Reactions & Stoichiometry

CHEM 50 — General Chemistry I · Dr. Karmach

build Jul 13 · 16:10 · CC BY-NC-SA 4.0 · OpenStax Chemistry 2e where noted
Dr. Karmach

By the end of this unit, you can…

  • Balance any chemical equation with the smallest whole-number coefficients
  • Read a balanced equation as a recipe: coefficients are mole relationships
  • Convert between amounts of any two species using mole ratios
  • Chain molar masses with mole ratios to solve gram-to-gram problems
  • Identify which reactant limits a reaction and how much product it allows
  • Classify a reaction by type and cite the evidence that a reaction occurred
  • Apply the solubility rules to predict precipitates and assign physical states
  • Write molecular, complete ionic, and net ionic equations and classify electrolytes
  • Assign oxidation numbers and identify oxidizing and reducing agents
  • Carry molarity through stoichiometric calculations and compute percent yield
Dr. Karmach

Today's route 🗺️

  1. Balancing Equations
  2. Mole Ratios
  3. Mass-to-Mass Stoichiometry
  4. Limiting Reactant
  5. Solution Stoichiometry
  6. Types of Reactions
  7. Solubility Rules & Precipitation
  8. Net Ionic Equations
  9. Electrolytes & Dissociation
  10. Oxidation Numbers
  11. Oxidizing & Reducing Agents
  12. Percent Yield
Dr. Karmach

1 · Balancing Equations

Turn any skeleton equation into a balanced one, and identify which numbers may change.

Dr. Karmach

Atoms don't disappear

Burning methane makes new molecules out of the same atoms. Count them: 1 C, 4 H, 4 O before and after. Every reaction works this way.

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Why every equation must balance

A reaction rearranges atoms. It never creates or destroys them. Both sides of a correct equation must show the same number of each kind of atom.

2 H₂ + O₂ → 2 H₂O
H: 4 = 4 ✓  ·  O: 2 = 2 ✓ — a possible reaction
H₂ + O₂ → H₂O
H: 2 = 2 ✓  ·  O: 2 ≠ 1 ✗ — an O atom would have to vanish
Dr. Karmach

What "balanced" looks like

2 KClO₃ → 2 KCl + 3 O₂
K: 2 = 2 ✓  ·  Cl: 2 = 2 ✓  ·  O: 6 = 6 ✓

Every element's count matches. That is the complete test.

Dr. Karmach

Coefficients and subscripts

2 H₂O
the 2 in front counts molecules  ·  the ₂ inside is part of the formula

An equation holds two kinds of numbers, and they do different jobs. Balancing may change only one of them.

Dr. Karmach

The method

  1. Write the atom count for each side.
  2. Balance one element at a time. Save any element that appears in several formulas for last.
  3. Recheck every count after each change.
  4. Finish with the smallest whole numbers.
Dr. Karmach

Worked example 1 — splitting water

Step 1 · Write the atom count for each side

H₂O → H₂ + O₂  (skeleton)
H: 2 = 2 ✓  ·  O: 1 ≠ 2 ✗

Electrolysis splits water into hydrogen gas and oxygen gas. Oxygen doesn't balance.

A common first attempt: change H₂O to H₂O₂. Test it.

Dr. Karmach

Worked example 1 — solution

H₂O → H₂ + O₂  (skeleton)
H: 2 = 2 ✓  ·  O: 1 ≠ 2 ✗

A common first attempt

H₂O₂ → H₂ + O₂
H: 2 = 2 ✓  ·  O: 2 = 2 ✓

Every count matches. But H₂O₂ is hydrogen peroxide. The goal was to split water; this equation splits a different substance. Changing a subscript changed the chemistry.

Dr. Karmach

Worked example 1 — solution

H₂O → H₂ + O₂  (skeleton)
H: 2 = 2 ✓  ·  O: 1 ≠ 2 ✗
A common first attempt
H₂O₂ → H₂ + O₂
H: 2 = 2 ✓  ·  O: 2 = 2 ✓
Step 2 · Balance one element at a time

Coefficients, not subscripts:

2 H₂O → 2 H₂ + O₂
H: 4 = 4 ✓  ·  O: 2 = 2 ✓
Dr. Karmach

Worked example 1 — solution

H₂O → H₂ + O₂  (skeleton)
H: 2 = 2 ✓  ·  O: 1 ≠ 2 ✗
A common first attempt
H₂O₂ → H₂ + O₂
H: 2 = 2 ✓  ·  O: 2 = 2 ✓
Step 2 · Balance one element at a time
2 H₂O → 2 H₂ + O₂
H: 4 = 4 ✓  ·  O: 2 = 2 ✓
Coefficients change the amount. Subscripts change the substance. Only coefficients may change.
Dr. Karmach

Take-home: coefficients, not subscripts

A coefficient counts molecules. A subscript is part of the formula.

Balancing may change only the coefficients.

Dr. Karmach

Worked example 2 — a common multiple

Rust: iron reacting with oxygen.

Step 1 · Write the atom count for each side

Fe + O₂ → Fe₂O₃  (skeleton)
Fe: 1 ≠ 2  ·  O: 2 ≠ 3

Oxygen shows 2 on the left and 3 on the right. What is the smallest number both divide into?

Dr. Karmach

Worked example 2 — solution

Fe + O₂ → Fe₂O₃  (skeleton)
Fe: 1 ≠ 2  ·  O: 2 ≠ 3

Step 2 · Balance one element at a time

O first, using the common multiple, 6: write 3 O₂ and 2 Fe₂O₃.

Fe + 3 O₂ → 2 Fe₂O₃
O: 6 = 6 ✓  ·  Fe: 1 ≠ 4 ✗

Fixing O changed the Fe count.

Dr. Karmach

Worked example 2 — solution

Fe + O₂ → Fe₂O₃  (skeleton)
Fe: 1 ≠ 2  ·  O: 2 ≠ 3
Step 2 · Balance one element at a time
Fe + 3 O₂ → 2 Fe₂O₃
O: 6 = 6 ✓  ·  Fe: 1 ≠ 4 ✗
Step 3 · Recheck every count

The recheck shows Fe unbalanced. Write 4 Fe:

4 Fe + 3 O₂ → 2 Fe₂O₃
Fe: 4 = 4 ✓  ·  O: 6 = 6 ✓
Dr. Karmach

Worked example 2 — solution

Fe + O₂ → Fe₂O₃  (skeleton)
Fe: 1 ≠ 2  ·  O: 2 ≠ 3
Step 2 · Balance one element at a time
Fe + 3 O₂ → 2 Fe₂O₃
O: 6 = 6 ✓  ·  Fe: 1 ≠ 4 ✗
Step 3 · Recheck every count
4 Fe + 3 O₂ → 2 Fe₂O₃
Fe: 4 = 4 ✓  ·  O: 6 = 6 ✓
One change can unbalance an element already counted. Recheck every count after each change.
Dr. Karmach

Your turn — zinc and hydrochloric acid

Zn + HCl → ZnCl₂ + H₂
atom left right
Zn 1 1 ✓
H × 1 2
Cl × 1 2

One coefficient balances both H and Cl.

Dr. Karmach

Your turn — zinc and hydrochloric acid

Zn + HCl → ZnCl₂ + H₂
atom left right
Zn 1 1 ✓
H × 1 2
Cl × 1 2

One coefficient balances both H and Cl.

Zn + 2 HCl → ZnCl₂ + H₂
Zn: 1 = 1 ✓  ·  H: 2 = 2 ✓  ·  Cl: 2 = 2 ✓
Dr. Karmach

Where this goes wrong

Changing subscripts. Writing H₂O₂ balances the counts but changes the substance. If the formula changes, the chemistry changes.
Forgetting the unwritten 1. Zn + 2 HCl → ZnCl₂ + H₂ has coefficient sum 1 + 2 + 1 + 1 = 5, not 4. An unwritten coefficient is still a 1.
Reading coefficients as grams. 4 Fe + 3 O₂ does not mean "4 g and 3 g." Coefficients count particles or moles. Converting to mass requires the molar mass.
Stopping too early. 8 Fe + 6 O₂ → 4 Fe₂O₃ balances, but every coefficient divides by 2. Reduce to smallest whole numbers.
Dr. Karmach

Practice 1

4 NH₃ + 5 O₂ → 4 NO + 6 H₂O

Ammonia oxidation, the first step in making nitric acid for fertilizer. What does the 5 in front of O₂ mean?

  1. Each O₂ molecule contains 5 oxygen atoms.
  2. 5 molecules of O₂ react, or equally 5 moles, in proportion to the other coefficients.
  3. 5 grams of O₂ are consumed.
  4. Exactly 5 individual molecules react. The number cannot scale up to moles.
Dr. Karmach

Practice 1 — answer: B

4 NH₃ + 5 O₂ → 4 NO + 6 H₂O
5 O₂ → 5 × 2 = 10 O  ·  right side: 4 NO + 6 H₂O → 4 + 6 = 10 O ✓

A describes a subscript's job. C: coefficients are counts, never masses. D: multiplying every coefficient by Avogadro's number leaves the ratios unchanged, so coefficients count moles as well as molecules.

In 5 O₂, the coefficient and the subscript do different jobs: 5 × 2 = 10 atoms of O.
Dr. Karmach

Worked example 3 — combustion

Butane fuels lighters.

Step 1 · Write the atom count for each side

C₄H₁₀ + O₂ → CO₂ + H₂O  (skeleton)
C: 4 ≠ 1  ·  H: 10 ≠ 2  ·  O: 2 ≠ 3

For combustion, balance C first, H second, O last. O₂ contains only one element, so its coefficient can be set last.

Balance it. A fraction will appear along the way.

Dr. Karmach

Worked example 3 — solution

C₄H₁₀ + O₂ → CO₂ + H₂O  (skeleton)

Step 2 · Balance one element at a time

C first: write 4 CO₂. Then H: write 5 H₂O.

C₄H₁₀ + O₂ → 4 CO₂ + 5 H₂O
C: 4 = 4 ✓  ·  H: 10 = 10 ✓  ·  O: 2 ≠ 13 ✗
Dr. Karmach

Worked example 3 — solution

C₄H₁₀ + O₂ → CO₂ + H₂O  (skeleton)
Step 2 · Balance one element at a time Step 3 · Recheck every count Step 4 · Finish with the smallest whole numbers

O last: the right side holds 13 O. Each O₂ supplies 2, so write 13/2 O₂, then double every coefficient.

step equation
C, then H C₄H₁₀ + O₂ → 4 CO₂ + 5 H₂O
O: right side holds 13 C₄H₁₀ + 13/2 O₂ → 4 CO₂ + 5 H₂O
double it 2 C₄H₁₀ + 13 O₂ → 8 CO₂ + 10 H₂O
2 C₄H₁₀ + 13 O₂ → 8 CO₂ + 10 H₂O
C: 8 = 8 ✓  ·  H: 20 = 20 ✓  ·  O: 26 = 26 ✓
Dr. Karmach

Worked example 3 — solution

C₄H₁₀ + O₂ → CO₂ + H₂O  (skeleton)
Step 2 · Balance one element at a time Step 3 · Recheck every count Step 4 · Finish with the smallest whole numbers
step equation
C, then H C₄H₁₀ + O₂ → 4 CO₂ + 5 H₂O
O: right side holds 13 C₄H₁₀ + 13/2 O₂ → 4 CO₂ + 5 H₂O
double it 2 C₄H₁₀ + 13 O₂ → 8 CO₂ + 10 H₂O
2 C₄H₁₀ + 13 O₂ → 8 CO₂ + 10 H₂O
C: 8 = 8 ✓  ·  H: 20 = 20 ✓  ·  O: 26 = 26 ✓
13 is odd, so no common factor remains. These are already the smallest whole numbers.
Dr. Karmach

Practice 2 — combustion

C₂H₄ + O₂ → CO₂ + H₂O  (skeleton)

Ethylene, the gas that ripens fruit, burns in air. Balance with smallest whole numbers. What is the sum of all the coefficients, counting every unwritten 1?

  1. 7
  2. 16
  3. 8
  4. 12
Dr. Karmach

Practice 2 — answer: C

C₂H₄ + O₂ → CO₂ + H₂O  (skeleton)
C₂H₄ + 3 O₂ → 2 CO₂ + 2 H₂O
1 + 3 + 2 + 2 = 8

C first (2 CO₂), H next (2 H₂O), O last: the right side holds 2 × 2 + 2 = 6, so 3 O₂. A omitted the unwritten 1: 3 + 2 + 2 = 7. B doubled every coefficient without reducing: 2 × 8 = 16. D doubled only the products: 1 + 3 + 4 + 4 = 12, and the O count no longer balances.

O check: left 3 × 2 = 6, right 2 × 2 + 2 = 6 ✓. The unwritten 1 is still included in the sum.
Dr. Karmach

Check yourself

  1. In 2 Al₂O₃, how many Al atoms in total? Which of the two numbers may change during balancing?
  2. Why is changing a subscript always wrong, even when the counts match?

These coefficients become mole ratios: the conversion factors used in every stoichiometry calculation.

Dr. Karmach

2 · Mole Ratios

Use the coefficients of a balanced equation to convert moles of one substance into moles of any other.

Dr. Karmach

The airbag problem

In a crash, an airbag pellet of sodium azide decomposes into nitrogen gas: 67 liters in 30 milliseconds. Mole ratios determine how much solid to pack.

Dr. Karmach

Why coefficients mean moles

2 C₂H₂ + 5 O₂ → 4 CO₂ + 2 H₂O
2 : 5 : 4 : 2 molecules2 : 5 : 4 : 2 dozen2 : 5 : 4 : 2 mol — the same ratio at every scale

A balanced equation counts molecules. Multiplying every amount by the same number leaves the ratio unchanged. Avogadro's number is one such multiplier, so coefficients count moles too.

Dr. Karmach

Reading the coefficients

2 C₂H₂ + 5 O₂ → 4 CO₂ + 2 H₂O

The coefficients count the molecules in the figure. The same numbers apply in moles. Like a recipe, the amounts scale together.

Dr. Karmach

Coefficients become conversion factors

2 C₂H₂ + 5 O₂ → 4 CO₂ + 2 H₂O

Any two coefficients form a mole ratio: a fraction that converts moles of one substance into moles of another.

4 mol CO₂5 mol O₂ or 5 mol O₂2 mol C₂H₂ or any pair

Write it so the given unit cancels.

Dr. Karmach

The method

  1. Start from a balanced equation. An unbalanced equation gives wrong ratios.
  2. Build the ratio wanted over given, so the given unit is in the denominator.
  3. Multiply, cancel the given unit, and check the result against the coefficients.
Dr. Karmach

Worked example 1

Step 1 · Start from a balanced equation

2 C₂H₂ + 5 O₂ → 4 CO₂ + 2 H₂O
given: 4.5 mol C₂H₂ · wanted: mol CO₂

A welding torch burns 4.5 mol of C₂H₂. How many moles of CO₂ form?

Set it up: which ratio cancels mol C₂H₂?

Dr. Karmach

Worked example 1 — solution

2 C₂H₂ + 5 O₂ → 4 CO₂ + 2 H₂O
given: 4.5 mol C₂H₂

One conversion factor is needed.

Step 2 · Build the ratio, wanted over given

Two orientations exist. Only one cancels the given unit:

4 mol CO₂2 mol C₂H₂ cancels mol C₂H₂ ✓    2 mol C₂H₂4 mol CO₂ cancels nothing ✗
Dr. Karmach

Worked example 1 — solution

2 C₂H₂ + 5 O₂ → 4 CO₂ + 2 H₂O
given: 4.5 mol C₂H₂
Step 2 · Build the ratio, wanted over given
4 mol CO₂2 mol C₂H₂ cancels mol C₂H₂ ✓    2 mol C₂H₂4 mol CO₂ cancels nothing ✗
Step 3 · Multiply and cancel
4.5 mol C₂H₂ × 4 mol CO₂2 mol C₂H₂ = 9.0 mol CO₂
Dr. Karmach

Worked example 1 — solution

2 C₂H₂ + 5 O₂ → 4 CO₂ + 2 H₂O
given: 4.5 mol C₂H₂
Step 2 · Build the ratio, wanted over given
4 mol CO₂2 mol C₂H₂ cancels mol C₂H₂ ✓    2 mol C₂H₂4 mol CO₂ cancels nothing ✗
Step 3 · Multiply and cancel
4.5 mol C₂H₂ × 4 mol CO₂2 mol C₂H₂ = 9.0 mol CO₂
The coefficients make CO₂ double the C₂H₂ (4 vs 2), and 9.0 is double 4.5. ✓
Dr. Karmach

Worked example 2

Step 1 · Start from a balanced equation

2 C₂H₂ + 5 O₂ → 4 CO₂ + 2 H₂O
given: 3.2 mol C₂H₂ · wanted: mol O₂

How many moles of O₂ does the torch consume while burning 3.2 mol C₂H₂?

Dr. Karmach

Worked example 2 — solution

2 C₂H₂ + 5 O₂ → 4 CO₂ + 2 H₂O
given: 3.2 mol C₂H₂

Step 2 · Build the ratio, wanted over given

The wanted substance is O₂, so the ratio is written O₂ over C₂H₂.

Dr. Karmach

Worked example 2 — solution

2 C₂H₂ + 5 O₂ → 4 CO₂ + 2 H₂O
given: 3.2 mol C₂H₂

Step 2 · Build the ratio, wanted over given

The wanted substance is O₂, so the ratio is written O₂ over C₂H₂.
Step 3 · Multiply and cancel

3.2 mol C₂H₂ × 5 mol O₂2 mol C₂H₂ = 8.0 mol O₂
Dr. Karmach

Worked example 2 — solution

2 C₂H₂ + 5 O₂ → 4 CO₂ + 2 H₂O
given: 3.2 mol C₂H₂

Step 2 · Build the ratio, wanted over given

The wanted substance is O₂, so the ratio is written O₂ over C₂H₂.
Step 3 · Multiply and cancel

3.2 mol C₂H₂ × 5 mol O₂2 mol C₂H₂ = 8.0 mol O₂
O₂'s coefficient (5) is larger than C₂H₂'s (2), so the torch needs more O₂ than fuel: 8.0 > 3.2. ✓
Dr. Karmach

Your turn — ammonia synthesis

N₂ + 3 H₂ → 2 NH₃

Making ammonia from 6.0 mol H₂:

6.0 mol H₂ × mol NH₃ mol H₂ = mol NH₃

Fill the ratio from the coefficients, then compute.

Dr. Karmach

Your turn — ammonia synthesis

N₂ + 3 H₂ → 2 NH₃

Making ammonia from 6.0 mol H₂:

6.0 mol H₂ × mol NH₃ mol H₂ = mol NH₃

Fill the ratio from the coefficients, then compute.

6.0 mol H₂ × 2 mol NH₃3 mol H₂ = 4.0 mol NH₃
Dr. Karmach

Where this goes wrong

N₂ + 3 H₂ → 2 NH₃
Assuming 1:1. "6 mol H₂ → 6 mol NH₃." The equation gives a 2 NH₃ : 3 H₂ ratio, so the answer is 4.0 mol.
Inverting the ratio. (3 mol H₂ / 2 mol NH₃) leaves units of mol H₂²/mol NH₃. Nothing cancels. If the units do not cancel, the fraction is inverted.
Answering with the coefficient. The coefficient (2) is not the answer. It must be applied to the given amount.
Dr. Karmach

Practice 1

2 H₂ + O₂ → 2 H₂O

7.0 mol of O₂ react completely. How many moles of H₂O form?

  1. 7.0 mol
  2. 14.0 mol
  3. 3.5 mol
  4. 2.0 mol
Dr. Karmach

Practice 1 — answer: B

2 H₂ + O₂ → 2 H₂O
given: 7.0 mol O₂
7.0 mol O₂ × 2 mol H₂O1 mol O₂ = 14.0 mol H₂O — answer B

A assumed 1:1: 7.0 × 1 = 7.0. C inverted the ratio: 7.0 × (1/2) = 3.5. D answered with the coefficient, 2.

Water's coefficient is double O₂'s, so the answer is double the given. ✓
Dr. Karmach

Practice 2

Fe₂O₃ + 3 CO → 2 Fe + 3 CO₂

A blast furnace is fed 4.8 mol CO. How many moles of iron form?

  1. 4.8 mol
  2. 7.2 mol
  3. 3.2 mol
  4. 9.6 mol
Dr. Karmach

Practice 2 — answer: C

Fe₂O₃ + 3 CO → 2 Fe + 3 CO₂
given: 4.8 mol CO
4.8 mol CO × 2 mol Fe3 mol CO = 3.2 mol Fe — answer C

A assumed 1:1: 4.8 × 1 = 4.8. B inverted the ratio: 4.8 × (3/2) = 7.2. D doubled the given: 4.8 × 2 = 9.6.

Fe's coefficient (2) is smaller than CO's (3), so less Fe forms than CO reacts: 3.2 < 4.8 ✓
Dr. Karmach

Worked example 3 — moles of reactant needed

Step 1 · Start from a balanced equation

2 KClO₃ → 2 KCl + 3 O₂
K: 2 = 2 ✓  ·  Cl: 2 = 2 ✓  ·  O: 6 = 6 ✓  ·  given: 7.5 mol O₂ · wanted: mol KClO₃

Heating potassium chlorate releases oxygen gas, one design for emergency oxygen generators. A generator must deliver 7.5 mol of O₂. How many moles of KClO₃ must it hold?

The given sits on the product side. The steps do not change.

Dr. Karmach

Worked example 3 — solution

2 KClO₃ → 2 KCl + 3 O₂
given: 7.5 mol O₂ · wanted: mol KClO₃

One conversion factor is needed.

Step 2 · Build the ratio, wanted over given

The ratio, wanted on top: 2 mol KClO₃ over 3 mol O₂, so mol O₂ cancels.

Dr. Karmach

Worked example 3 — solution

2 KClO₃ → 2 KCl + 3 O₂
given: 7.5 mol O₂ · wanted: mol KClO₃
Step 2 · Build the ratio, wanted over given Step 3 · Multiply and cancel
7.5 mol O₂ × 2 mol KClO₃3 mol O₂ = 5.0 mol KClO₃
Dr. Karmach

Worked example 3 — solution

2 KClO₃ → 2 KCl + 3 O₂
given: 7.5 mol O₂ · wanted: mol KClO₃
Step 2 · Build the ratio, wanted over given Step 3 · Multiply and cancel
7.5 mol O₂ × 2 mol KClO₃3 mol O₂ = 5.0 mol KClO₃
Fewer moles of solid are packed than moles of gas delivered: 2 KClO₃ yield 3 O₂. The ratio converts in either direction across the equation. ✓
Dr. Karmach

Practice 3

2 C₄H₁₀ + 13 O₂ → 8 CO₂ + 10 H₂O

Greenhouse growers burn butane to enrich the air with CO₂, which speeds plant growth. How many moles of C₄H₁₀ must burn to produce 26.0 mol of CO₂?

  1. 26.0 mol
  2. 52.0 mol
  3. 6.50 mol
  4. 104 mol
Dr. Karmach

Practice 3 — answer: C

2 C₄H₁₀ + 13 O₂ → 8 CO₂ + 10 H₂O
given: 26.0 mol CO₂ · wanted: mol C₄H₁₀
26.0 mol CO₂ × 2 mol C₄H₁₀8 mol CO₂ = 6.50 mol C₄H₁₀ — answer C

A assumed a 1 : 1 ratio: 26.0 × 1 = 26.0. B multiplied by 2 without dividing by 8: 26.0 × 2 = 52.0. D inverted the ratio: 26.0 × (8/2) = 104.

The ratio 8 : 2 means four CO₂ per butane, so the fuel needed is 26.0 ÷ 4 = 6.50 mol. ✓
Dr. Karmach

Check yourself

  1. Why does a mole ratio require moles, not grams? (What do coefficients count?)
  2. In N₂ + 3 H₂ → 2 NH₃, which ratio converts mol N₂ → mol NH₃?

A molar-mass conversion on each end of the mole ratio extends this to grams → grams: mass-to-mass stoichiometry. Given two reactants, the same ratios show which one runs out first.

Dr. Karmach

3 · Mass-to-Mass Stoichiometry

Convert a given mass of one substance into the mass of another by converting grams to moles, crossing substances with the mole ratio, and converting back.

Dr. Karmach

Heavier than the fuel

One 45-kg tank of gasoline emits about 140 kg of CO₂ — triple the fuel's mass. The extra mass comes from oxygen in the air, and stoichiometry predicts it exactly.

Dr. Karmach

Equations count particles, not grams

C₆H₁₂O₆ + 6 O₂ → 6 CO₂ + 6 H₂O
moles — 1 glucose : 6 CO₂  ·  grams — 180.16 : 264.06, not 1 : 6

A balanced equation relates counts (moles), never masses. A mole of glucose weighs four times a mole of CO₂, so a 1:6 mole ratio is not a 1:6 gram ratio.

Dr. Karmach

Convert to moles, then convert back

Convert the given mass to moles, relate moles with the equation, and convert back to mass at the end.

Dr. Karmach

The full map

Mass, molecules, or atoms on either side: convert in to moles, cross the mole ratio, convert out.

Dr. Karmach

Three conversion factors, one setup

Molar mass converts at each end; the mole ratio is the only factor that switches substances. Chain them so each unit cancels the one before:

g A × 1 mol A(molar mass A) g A × b mol Ba mol A × (molar mass B) g B1 mol B = g B
Dr. Karmach

The method

  1. Grams → moles: convert the given mass with its own molar mass.
  2. Moles → moles: cross substances with the mole ratio. No other step can.
  3. Moles → grams: convert out with the target's molar mass.
Dr. Karmach

Worked example 1

C₆H₁₂O₆ + 6 O₂ → 6 CO₂ + 6 H₂O
given: 90.0 g glucose · wanted: g CO₂

Respiration burns glucose, and the CO₂ is exhaled. What mass of CO₂ forms when 90.0 g of glucose reacts completely? (glucose 180.16 g/mol, CO₂ 44.01 g/mol)

Write the route first: g glucose → mol glucose → mol CO₂ → g CO₂.

Dr. Karmach

Worked example 1 — solution

C₆H₁₂O₆ + 6 O₂ → 6 CO₂ + 6 H₂O
given: 90.0 g glucose

Three conversion factors are needed.

Step 1 · Grams → moles

Glucose's own molar mass converts the given mass to moles. Its unit cancels the given unit:

90.0 g glucose × 1 mol glucose180.16 g glucose
Dr. Karmach

Worked example 1 — solution

C₆H₁₂O₆ + 6 O₂ → 6 CO₂ + 6 H₂O
given: 90.0 g glucose
Step 1 · Grams → moles
90.0 g glucose × 1 mol glucose180.16 g glucose
Step 2 · Moles → moles

The mole ratio is the only factor that crosses substances. Two orientations exist. Only one cancels mol glucose:

6 mol CO₂1 mol glucose cancels mol glucose ✓    1 mol glucose6 mol CO₂ cancels nothing ✗
Dr. Karmach

Worked example 1 — solution

C₆H₁₂O₆ + 6 O₂ → 6 CO₂ + 6 H₂O
given: 90.0 g glucose
Step 1 · Grams → moles
90.0 g glucose × 1 mol glucose180.16 g glucose
Step 2 · Moles → moles Step 3 · Moles → grams

Convert out with the target's molar mass, in one continuous setup. Carry all digits and round once at the end:

90.0 g glucose × 1 mol glucose180.16 g glucose × 6 mol CO₂1 mol glucose × 44.01 g CO₂1 mol CO₂ = 132 g CO₂
Dr. Karmach

Worked example 1 — solution

C₆H₁₂O₆ + 6 O₂ → 6 CO₂ + 6 H₂O
given: 90.0 g glucose
Step 1 · Grams → moles
90.0 g glucose × 1 mol glucose180.16 g glucose
Step 2 · Moles → moles Step 3 · Moles → grams
90.0 g glucose × 1 mol glucose180.16 g glucose × 6 mol CO₂1 mol glucose × 44.01 g CO₂1 mol CO₂ = 132 g CO₂
More mass leaves than entered: the carbon leaves as CO₂, and the added oxygen mass comes from the air. The extra mass is oxygen from the air. ✓
Dr. Karmach

Worked example 2

3 Si + 2 Cr₂O₃ → 3 SiO₂ + 4 Cr
given: 42.0 g Si · wanted: g Cr

Silicon extracts chromium metal from its ore. What mass of Cr forms when 42.0 g of Si reacts completely? (Si 28.09 g/mol, Cr 52.00 g/mol)

The equation is already balanced. Read the mole ratio directly from the coefficients.

Dr. Karmach

Worked example 2 — solution

3 Si + 2 Cr₂O₃ → 3 SiO₂ + 4 Cr
given: 42.0 g Si

Three conversion factors are needed.

Step 1 · Grams → moles

The molar mass, 28.09 g per mole, converts the given mass of Si to moles.

Dr. Karmach

Worked example 2 — solution

3 Si + 2 Cr₂O₃ → 3 SiO₂ + 4 Cr
given: 42.0 g Si
Step 1 · Grams → moles Step 2 · Moles → moles

The mole ratio, written Cr over Si (4 : 3), crosses substances; mol Si cancels. Only the substances changed; the route is the same.

Dr. Karmach

Worked example 2 — solution

3 Si + 2 Cr₂O₃ → 3 SiO₂ + 4 Cr
given: 42.0 g Si
Step 1 · Grams → moles Step 2 · Moles → moles Step 3 · Moles → grams

Convert out with Cr's molar mass. The complete chain:

42.0 g Si × 1 mol Si28.09 g Si × 4 mol Cr3 mol Si × 52.00 g Cr1 mol Cr = 104 g Cr

Label every quantity with its substance. A wrong setup shows up as a unit that will not cancel.

Dr. Karmach

Worked example 2 — solution

3 Si + 2 Cr₂O₃ → 3 SiO₂ + 4 Cr
given: 42.0 g Si
Step 1 · Grams → moles Step 2 · Moles → moles Step 3 · Moles → grams
42.0 g Si × 1 mol Si28.09 g Si × 4 mol Cr3 mol Si × 52.00 g Cr1 mol Cr = 104 g Cr
A mole of Cr (52.00 g) weighs nearly twice a mole of Si (28.09 g), and the ratio gives more moles of Cr (4:3). More mass leaves than entered: 104 > 42.0 ✓
Dr. Karmach

Your turn — potassium chlorate

2 KClO₃ → 2 KCl + 3 O₂

Heating potassium chlorate releases oxygen gas. Starting from 61.3 g KClO₃ (122.55 g/mol; O₂ 32.00 g/mol):

61.3 g KClO₃ × 1 mol KClO₃122.55 g KClO₃ × mol O₂ mol KClO₃ × g O₂1 mol O₂ = g O₂

Fill the mole ratio from the coefficients and the last molar mass, then compute.

Dr. Karmach

Your turn — potassium chlorate

2 KClO₃ → 2 KCl + 3 O₂

Heating potassium chlorate releases oxygen gas. Starting from 61.3 g KClO₃ (122.55 g/mol; O₂ 32.00 g/mol):

61.3 g KClO₃ × 1 mol KClO₃122.55 g KClO₃ × mol O₂ mol KClO₃ × g O₂1 mol O₂ = g O₂

Fill the mole ratio from the coefficients and the last molar mass, then compute.

61.3 g KClO₃ × 1 mol KClO₃122.55 g KClO₃ × 3 mol O₂2 mol KClO₃ × 32.00 g O₂1 mol O₂ = 24.0 g O₂
Dr. Karmach

Grams never enter the mole ratio

2 KClO₃ → 2 KCl + 3 O₂
given: 61.3 g KClO₃ · wanted: g O₂

Do: convert the given mass to moles first.

61.3 g ÷ 122.55 g/mol = 0.500 mol KClO₃
grams → moles with the molar mass ✓

Do not: apply the mole ratio to grams.

61.3 g × 3/2 = 92.0 g
coefficients count moles, not grams ✗
Dr. Karmach

Where this goes wrong

2 KClO₃ → 2 KCl + 3 O₂
given: 61.3 g KClO₃
Applying the mole ratio to grams. 61.3 g × (3/2) = 92.0 g is wrong: coefficients count moles, not grams. Convert first: 61.3 g ÷ 122.55 g/mol = 0.500 mol. The correct answer is 24.0 g.
Skipping the mole ratio. g → mol → g gives 16.0 g. That assumes a 1:1 ratio. The equation gives 2 KClO₃ : 3 O₂, and the mole ratio is the only step that switches substances.
Inverting the ratio. (2 mol KClO₃ / 3 mol O₂) leaves units of mol KClO₃²/mol O₂. Nothing cancels, and 10.7 g is wrong. If the units do not cancel, the fraction is inverted.
Dr. Karmach

Practice 1

C₃H₈ + 5 O₂ → 3 CO₂ + 4 H₂O

A camping stove burns 25.0 g of propane (44.09 g/mol). What mass of water forms? (H₂O 18.02 g/mol)

  1. 10.2 g
  2. 100. g
  3. 40.9 g
  4. 2.55 g
Dr. Karmach

Practice 1 — answer: C

C₃H₈ + 5 O₂ → 3 CO₂ + 4 H₂O
given: 25.0 g C₃H₈
25.0 g C₃H₈ × 1 mol C₃H₈44.09 g C₃H₈ × 4 mol H₂O1 mol C₃H₈ × 18.02 g H₂O1 mol H₂O = 40.9 g H₂O — answer C

A skipped the mole ratio: 25.0/44.09 × 18.02 = 10.2. B applied the ratio to grams: 25.0 × 4 = 100. D inverted the ratio: 25.0/44.09 × (1/4) × 18.02 = 2.55.

The ratio gives four H₂O per C₃H₈, but a mole of H₂O weighs less than half a mole of C₃H₈ (18 vs 44 g). The overall factor is about 1.6: 25.0 → 40.9 ✓
Dr. Karmach

Practice 2

4 Al + 3 O₂ → 2 Al₂O₃

35.0 g of aluminum (26.98 g/mol) oxidizes completely. What mass of Al₂O₃ (101.96 g/mol) forms?

  1. 17.5 g
  2. 66.1 g
  3. 132 g
  4. 265 g
Dr. Karmach

Practice 2 — answer: B

4 Al + 3 O₂ → 2 Al₂O₃
given: 35.0 g Al
35.0 g Al × 1 mol Al26.98 g Al × 2 mol Al₂O₃4 mol Al × 101.96 g Al₂O₃1 mol Al₂O₃ = 66.1 g Al₂O₃ — answer B

A applied the ratio to grams: 35.0 × (2/4) = 17.5. C skipped the mole ratio: 35.0/26.98 × 101.96 = 132. D inverted the ratio: 35.0/26.98 × (4/2) × 101.96 = 265.

The oxide weighs more than the metal alone. The extra 31 g is oxygen from the air. ✓
Dr. Karmach

Check yourself

  1. In the g → g route, why must the given mass become moles before the mole ratio is applied? (What do coefficients count?)
  2. Fill in the route: g A → ? → ? → g B. Which of the three factors is the only one that switches substances?

Many problems give two starting masses. Convert each reactant to the same product; whichever gives less product runs out first. That is the limiting reactant.

Dr. Karmach

4 · Limiting Reactant

Decide which reactant runs out first, and compute the product from that reactant alone.

Dr. Karmach

One ingredient runs out first

One bun and one patty per burger. The patties ran out first, so only seven burgers can be made. Reactions work the same way, in moles.

Dr. Karmach

Reactants are consumed in a fixed ratio

2 H₂ + O₂ → 2 H₂O

A reaction consumes its reactants in a fixed ratio, set by the coefficients. One reactant runs out first; the reaction stops there.

Dr. Karmach

The reaction stops when one runs out

2 Al + Fe₂O₃ → Al₂O₃ + 2 Fe

The reaction runs only while both reactants remain. The first to run out is the limiting reactant; it sets the maximum product. The unreacted portion of the other is excess.

Dr. Karmach

The test: moles ÷ coefficient

2 H₂ + O₂ → 2 H₂O

The coefficients set the proportion in which the reactants are consumed. Divide each reactant's moles by its coefficient. The smaller result marks the limiting reactant.

H₂: 6.0 mol2 = 3.0 ← smaller: H₂ limits
O₂: 4.0 mol1 = 4.0 (excess)

O₂ has fewer moles, yet H₂ runs out first.

Dr. Karmach

The method

  1. Convert both reactants to moles.
  2. Divide each by its coefficient.
  3. The smaller number limits: that reactant runs out first.
  4. Compute product from the limiting reactant only.
Dr. Karmach

Worked example 1 — thermite

2 Al + Fe₂O₃ → Al₂O₃ + 2 Fe
given: 4.6 mol Al and 3.8 mol Fe₂O₃

Rail-welding thermite: 4.6 mol Al mixed with 3.8 mol Fe₂O₃. How many moles of Al₂O₃ can form?

Divide each reactant's moles by its coefficient. The smaller result marks the limiting reactant.

Dr. Karmach

Worked example 1 — which reactant limits

2 Al + Fe₂O₃ → Al₂O₃ + 2 Fe
given: 4.6 mol Al and 3.8 mol Fe₂O₃

Step 1 · Convert both reactants to moles

Both amounts are already in moles, so Step 1 is complete.

Step 2 · Divide each by its coefficient

Al: 4.6 mol2 = 2.3
Dr. Karmach

Worked example 1 — which reactant limits

2 Al + Fe₂O₃ → Al₂O₃ + 2 Fe
given: 4.6 mol Al and 3.8 mol Fe₂O₃
Step 1 · Convert both reactants to moles Step 2 · Divide each by its coefficient
Al: 4.6 mol2 = 2.3
Fe₂O₃: the same division.
Fe₂O₃: 3.8 mol1 = 3.8
Dr. Karmach

Worked example 1 — which reactant limits

2 Al + Fe₂O₃ → Al₂O₃ + 2 Fe
given: 4.6 mol Al and 3.8 mol Fe₂O₃
Step 1 · Convert both reactants to moles Step 2 · Divide each by its coefficient
Al: 4.6 mol2 = 2.3
Fe₂O₃: 3.8 mol1 = 3.8
Step 3 · The smaller number limits
2.3 < 3.8, so Al limits. Fe₂O₃ is excess.
Dr. Karmach

Worked example 1 — how much product

2 Al + Fe₂O₃ → Al₂O₃ + 2 Fe
given: 4.6 mol Al and 3.8 mol Fe₂O₃ · Al limits

Step 4 · Compute product from the limiting reactant only

4.6 mol Al × 1 mol Al₂O₃2 mol Al = 2.3 mol Al₂O₃
Dr. Karmach

Worked example 1 — how much product

2 Al + Fe₂O₃ → Al₂O₃ + 2 Fe
given: 4.6 mol Al and 3.8 mol Fe₂O₃ · Al limits

Step 4 · Compute product from the limiting reactant only

4.6 mol Al × 1 mol Al₂O₃2 mol Al = 2.3 mol Al₂O₃
Fe₂O₃ alone could give 3.8 mol, but the reaction stops when Al runs out, at 2.3 mol. The smaller result is the amount that can actually form. ✓
Dr. Karmach

Worked example 2 — full mass chain

N₂ + 3 H₂ → 2 NH₃
given: 42.0 g N₂ and 12.0 g H₂

An ammonia reactor is charged with 42.0 g N₂ and 12.0 g H₂. What mass of NH₃ can form?

A common first attempt: H₂ has the smaller mass, 12.0 g, so H₂ limits. Test it.

Dr. Karmach

Worked example 2 — which reactant limits

N₂ + 3 H₂ → 2 NH₃ · given: 42.0 g N₂ and 12.0 g H₂

Four conversion factors are needed: one molar mass for each reactant, then the mole ratio, then the target's molar mass.

Step 1 · Convert both reactants to moles

42.0 g N₂ × 1 mol N₂28.02 g N₂ = 1.50 mol N₂ · 12.0 g H₂ × 1 mol H₂2.016 g H₂ = 5.95 mol H₂
Dr. Karmach

Worked example 2 — which reactant limits

N₂ + 3 H₂ → 2 NH₃ · given: 42.0 g N₂ and 12.0 g H₂
Step 1 · Convert both reactants to moles
42.0 g N₂ × 1 mol N₂28.02 g N₂ = 1.50 mol N₂ · 12.0 g H₂ × 1 mol H₂2.016 g H₂ = 5.95 mol H₂
Step 2 · Divide each by its coefficient
N₂: 1.50 mol1 = 1.50 · H₂: 5.95 mol3 = 1.98
Dr. Karmach

Worked example 2 — which reactant limits

N₂ + 3 H₂ → 2 NH₃ · given: 42.0 g N₂ and 12.0 g H₂
Step 1 · Convert both reactants to moles
42.0 g N₂ × 1 mol N₂28.02 g N₂ = 1.50 mol N₂ · 12.0 g H₂ × 1 mol H₂2.016 g H₂ = 5.95 mol H₂
Step 2 · Divide each by its coefficient
N₂: 1.50 mol1 = 1.50 · H₂: 5.95 mol3 = 1.98
Step 3 · The smaller number limits
1.50 < 1.98, so N₂ limits. H₂ is excess.
Dr. Karmach

Worked example 2 — how much product

N₂ + 3 H₂ → 2 NH₃
given: 42.0 g N₂ and 12.0 g H₂ · N₂ limits, 1.50 mol

Step 4 · Compute product from the limiting reactant only

1.50 mol N₂ × 2 mol NH₃1 mol N₂ × 17.03 g NH₃1 mol NH₃ = 51.1 g NH₃
Dr. Karmach

Worked example 2 — how much product

N₂ + 3 H₂ → 2 NH₃
given: 42.0 g N₂ and 12.0 g H₂ · N₂ limits, 1.50 mol

Step 4 · Compute product from the limiting reactant only

1.50 mol N₂ × 2 mol NH₃1 mol N₂ × 17.03 g NH₃1 mol NH₃ = 51.1 g NH₃
The smaller mass, 12.0 g of H₂, is the excess reactant. Mass does not identify the limiting reactant. ✓
Dr. Karmach

Take-home: mass does not pick the limiting reactant

N₂ + 3 H₂ → 2 NH₃
given: 42.0 g N₂ and 12.0 g H₂ — the larger mass limits
N₂: 1.50 mol1 = 1.50N₂ limits · H₂: 5.95 mol3 = 1.98 (excess)

The larger mass, 42.0 g of N₂, runs out first. Divide each reactant's moles by its coefficient; the smaller result limits.

Dr. Karmach

Your turn — finish the comparison

2 Mg + O₂ → 2 MgO

A signal flare holds 0.80 mol Mg and 0.50 mol O₂. How many moles of MgO form?

Mg: 0.80 mol2 = 0.40 · O₂: 0.50 mol1 =

Limiting reactant:

Dr. Karmach

Your turn — finish the comparison

2 Mg + O₂ → 2 MgO

A signal flare holds 0.80 mol Mg and 0.50 mol O₂. How many moles of MgO form?

Mg: 0.80 mol2 = 0.40 · O₂: 0.50 mol1 =

Limiting reactant:

O₂: 0.50 / 1 = 0.50 · Mg: 0.40 is smaller, so Mg limits · 0.80 mol Mg × 2 mol MgO2 mol Mg = 0.80 mol MgO
Dr. Karmach

Where this goes wrong

Picking the limiting reactant by mass. In N₂ + 3 H₂ → 2 NH₃, the smaller mass, 12.0 g of H₂ against 42.0 g of N₂, is the excess. Mass does not identify the limiting reactant; moles ÷ coefficient does.
Comparing raw moles. In 2 Mg + O₂ → 2 MgO, 0.50 mol O₂ is fewer moles than 0.80 mol Mg. But two Mg are consumed per O₂: 0.40 vs 0.50, so Mg limits and 0.80 mol MgO forms.
2 Al + Fe₂O₃ → Al₂O₃ + 2 Fe
given: 4.6 mol Al and 3.8 mol Fe₂O₃
Building product from the excess reactant. With 4.6 mol Al and 3.8 mol Fe₂O₃, the 3.8 mol suggests 3.8 mol Al₂O₃. The reaction stops at 2.3 mol, when Al runs out. Compute product from the limiting reactant only.
Applying the mole ratio to grams. Coefficients count moles, not grams. Convert each mass to moles before comparing.
Dr. Karmach

Practice 1

Mg + 2 HCl → MgCl₂ + H₂

25.0 g of HCl is poured over 10.0 g of Mg. What is the maximum mass of MgCl₂? (HCl 36.46 g/mol · Mg 24.31 g/mol · MgCl₂ 95.21 g/mol)

  1. 12.5 g
  2. 39.2 g
  3. 32.6 g
  4. 65.3 g
Dr. Karmach

Practice 1 — answer: C

Mg + 2 HCl → MgCl₂ + H₂
given: 25.0 g HCl and 10.0 g Mg
HCl: 0.686 mol2 = 0.343HCl limits · Mg: 0.411 mol1 = 0.411 (excess)
25.0 g HCl × 1 mol HCl36.46 g HCl × 1 mol MgCl₂2 mol HCl × 95.21 g MgCl₂1 mol MgCl₂ = 32.6 g MgCl₂ — answer C

A applied the ratio to grams: 25.0 × (1/2) = 12.5. B built product from the excess Mg: 10.0/24.31 × 95.21 = 39.2. D skipped the mole ratio: 25.0/36.46 × 95.21 = 65.3.

Mg's mass is smaller (10.0 g vs 25.0 g), yet Mg is the excess: each Mg consumes two HCl. ✓
Dr. Karmach

Practice 2

C₃H₈ + 5 O₂ → 3 CO₂ + 4 H₂O

A camp stove burns 11.0 g of propane in 32.0 g of O₂. What is the maximum mass of CO₂? (C₃H₈ 44.09 g/mol · O₂ 32.00 g/mol · CO₂ 44.01 g/mol)

  1. 26.4 g
  2. 32.9 g
  3. 44.0 g
  4. 19.2 g
Dr. Karmach

Practice 2 — answer: A

C₃H₈ + 5 O₂ → 3 CO₂ + 4 H₂O
given: 11.0 g C₃H₈ and 32.0 g O₂
O₂: 1.00 mol5 = 0.200O₂ limits · C₃H₈: 0.249 mol1 = 0.249 (excess)
32.0 g O₂ × 1 mol O₂32.00 g O₂ × 3 mol CO₂5 mol O₂ × 44.01 g CO₂1 mol CO₂ = 26.4 g CO₂ — answer A

B built product from the excess propane: 11.0/44.09 × 3 × 44.01 = 32.9. C skipped the mole ratio: 1.00 × 44.01 = 44.0. D applied the ratio to grams: 32.0 × (3/5) = 19.2.

O₂ has more grams and more moles (1.00 vs 0.249), yet it runs out first: each propane consumes five O₂. ✓
Dr. Karmach

Check yourself

  1. Two reactant masses are given. List the steps that identify the limiting reactant. (Where do the coefficients enter?)
  2. Why does neither the smallest mass nor the fewest moles identify the limiting reactant?

The product the limiting reactant allows is the theoretical yield: the maximum the reaction can produce. Percent yield compares the amount actually collected to that maximum: actual over theoretical, × 100.

Dr. Karmach

5 · Solution Stoichiometry

Convert a volume of solution to moles with molarity, cross substances with the mole ratio, and finish in grams or in the volume of a second solution.

Dr. Karmach

Dosed by volume

A pool is chlorinated by pumping in a measured volume of chlorine solution. Nothing is weighed: the strength on the drum's label and the liters pumped set the chlorine dose.

Dr. Karmach

A solution's label counts moles

0.500 M NaOH — 0.500 mol NaOH = 1 L of solution
the label states a rate: moles delivered per liter poured

Measure a volume, and the label converts it to moles; the liters cancel:

0.2000 L soln × 0.500 mol NaOH1 L soln = 0.100 mol NaOH

A graduated cylinder now counts moles. No balance is needed.

Dr. Karmach

Two ways to deliver 0.100 mol

4.00 g NaOH ÷ 40.00 g/mol = 0.100 mol NaOH
counted with a balance and the molar mass
0.2000 L of 0.500 M NaOH = 0.100 mol NaOH
counted with a graduated cylinder and the label

A reaction receives 0.100 mol either way. Stoichiometry works on moles; where they came from never enters the calculation.

Dr. Karmach

Volume joins the map

Volume of solution enters through molarity, exactly where grams enter through molar mass. Every route still crosses the mole bridge, and the mole ratio still switches substances.

Dr. Karmach

The method

  1. Volume → moles: mL to L; molarity converts liters to moles of its solute.
  2. Moles → moles: cross substances with the mole ratio. No other step can.
  3. Moles → the wanted unit: molar mass for grams; molarity for volume.
Dr. Karmach

Worked example 1 — moles from a solution volume

Zn + 2 HCl → ZnCl₂ + H₂
given: 250.0 mL of 0.400 M HCl · wanted: mol H₂

Zinc metal dissolves in hydrochloric acid, releasing hydrogen gas. 250.0 mL of 0.400 M HCl reacts completely with excess zinc. How many moles of H₂ form?

Write the route first: mL → L → mol HCl → mol H₂.

Dr. Karmach

Worked example 1 — solution

Zn + 2 HCl → ZnCl₂ + H₂
given: 250.0 mL of 0.400 M HCl · wanted: mol H₂

Two conversion factors are needed.

Step 1 · Volume → moles

250.0 mL is 0.2500 L. The label's molarity converts the liters to moles of HCl:

0.2500 L soln × 0.400 mol HCl1 L soln = 0.100 mol HCl
Dr. Karmach

Worked example 1 — solution

Zn + 2 HCl → ZnCl₂ + H₂
given: 250.0 mL of 0.400 M HCl · wanted: mol H₂
Step 1 · Volume → moles
0.2500 L soln × 0.400 mol HCl1 L soln = 0.100 mol HCl
Step 2 · Moles → moles

The mole ratio, written H₂ over HCl (1 : 2), crosses substances; mol HCl cancels:

0.2500 L soln × 0.400 mol HCl1 L soln × 1 mol H₂2 mol HCl = 0.0500 mol H₂
Dr. Karmach

Worked example 1 — solution

Zn + 2 HCl → ZnCl₂ + H₂
given: 250.0 mL of 0.400 M HCl · wanted: mol H₂
Step 1 · Volume → moles
0.2500 L soln × 0.400 mol HCl1 L soln = 0.100 mol HCl
Step 2 · Moles → moles
0.2500 L soln × 0.400 mol HCl1 L soln × 1 mol H₂2 mol HCl = 0.0500 mol H₂
Each H₂ consumes two HCl, so the mole count halves: 0.100 mol HCl → 0.0500 mol H₂ ✓
Dr. Karmach

Worked example 2 — grams of product from a solution volume

Pb(NO₃)₂ + 2 KI → PbI₂ + 2 KNO₃
given: 150.0 mL of 0.300 M KI · wanted: g PbI₂

Two clear solutions mix, and bright yellow lead(II) iodide settles out. 150.0 mL of 0.300 M KI reacts completely with excess Pb(NO₃)₂. What mass of PbI₂ forms? (PbI₂ 461.0 g/mol)

A tempting shortcut: carry the moles of KI straight to grams of PbI₂. Test it against the equation.

Dr. Karmach

Worked example 2 — solution

Pb(NO₃)₂ + 2 KI → PbI₂ + 2 KNO₃
given: 150.0 mL of 0.300 M KI · wanted: g PbI₂ (461.0 g/mol)

Three conversion factors are needed.

Step 1 · Volume → moles

150.0 mL is 0.1500 L. The molarity, 0.300 mol per liter, converts the liters to 0.0450 mol KI.

Dr. Karmach

Worked example 2 — solution

Pb(NO₃)₂ + 2 KI → PbI₂ + 2 KNO₃
given: 150.0 mL of 0.300 M KI · wanted: g PbI₂ (461.0 g/mol)
Step 1 · Volume → moles The tempting shortcut
0.0450 mol KI × 461.0 g PbI₂1 mol PbI₂ = 20.7 g ✗

mol KI cannot cancel mol PbI₂. The equation makes one PbI₂ from two KI; the mole ratio must cross first.

Dr. Karmach

Worked example 2 — solution

Pb(NO₃)₂ + 2 KI → PbI₂ + 2 KNO₃
given: 150.0 mL of 0.300 M KI · wanted: g PbI₂ (461.0 g/mol)
Step 1 · Volume → moles The tempting shortcut
0.0450 mol KI × 461.0 g PbI₂1 mol PbI₂ = 20.7 g ✗
Step 2 · Moles → moles Step 3 · Moles → the wanted unit

The ratio, written PbI₂ over KI (1 : 2), crosses substances; the molar mass then converts out:

0.1500 L soln × 0.300 mol KI1 L soln × 1 mol PbI₂2 mol KI × 461.0 g PbI₂1 mol PbI₂ = 10.4 g PbI₂
Dr. Karmach

Worked example 2 — solution

Pb(NO₃)₂ + 2 KI → PbI₂ + 2 KNO₃
given: 150.0 mL of 0.300 M KI · wanted: g PbI₂ (461.0 g/mol)
Step 1 · Volume → moles The tempting shortcut
0.0450 mol KI × 461.0 g PbI₂1 mol PbI₂ = 20.7 g ✗
Step 2 · Moles → moles Step 3 · Moles → the wanted unit
0.1500 L soln × 0.300 mol KI1 L soln × 1 mol PbI₂2 mol KI × 461.0 g PbI₂1 mol PbI₂ = 10.4 g PbI₂
Two KI deliver one PbI₂: 0.0450 mol halves to 0.0225 mol, and each mole weighs 461.0 g — about 10 g. 10.4 g ✓
Dr. Karmach

Take-home: only the mole ratio switches substances

0.0450 mol KI × 461.0 g PbI₂1 mol PbI₂ = 20.7 g ✗ — nothing cancels
0.0450 mol KI × 1 mol PbI₂2 mol KI × 461.0 g PbI₂1 mol PbI₂ = 10.4 g PbI₂ ✓

Molarity delivers moles of its own solute, nothing else. In solution exactly as on a balance, only the mole ratio crosses to another substance.

Dr. Karmach

Your turn — copper(II) hydroxide

CuSO₄ + 2 NaOH → Cu(OH)₂ + Na₂SO₄
given: 200.0 mL (0.2000 L) of 0.250 M NaOH · wanted: g Cu(OH)₂ (97.57 g/mol)

Excess copper(II) sulfate reacts with 200.0 mL of 0.250 M NaOH, and pale blue Cu(OH)₂ precipitates:

0.2000 L soln × mol NaOH1 L soln × mol Cu(OH)₂ mol NaOH × g Cu(OH)₂1 mol Cu(OH)₂ = g Cu(OH)₂

Fill the molarity, the mole ratio, and the molar mass, then compute.

Dr. Karmach

Your turn — copper(II) hydroxide

CuSO₄ + 2 NaOH → Cu(OH)₂ + Na₂SO₄
given: 200.0 mL (0.2000 L) of 0.250 M NaOH · wanted: g Cu(OH)₂ (97.57 g/mol)
0.2000 L soln × mol NaOH1 L soln × mol Cu(OH)₂ mol NaOH × g Cu(OH)₂1 mol Cu(OH)₂ = g Cu(OH)₂
0.2000 L soln × 0.250 mol NaOH1 L soln × 1 mol Cu(OH)₂2 mol NaOH × 97.57 g Cu(OH)₂1 mol Cu(OH)₂ = 2.44 g Cu(OH)₂
Dr. Karmach

Where this goes wrong

Pb(NO₃)₂ + 2 KI → PbI₂ + 2 KNO₃
given: 150.0 mL of 0.300 M KI · correct: 0.1500 L → 0.0450 mol KI → 0.0225 mol PbI₂ → 10.4 g
Feeding milliliters to the molarity. 150.0 × 0.300 = 45.0 mol KI, a thousand times too many. Molarity counts liters of solution: 150.0 mL is 0.1500 L, and 0.1500 × 0.300 = 0.0450 mol.
Skipping the mole ratio. 0.0450 × 461.0 = 20.7 g assumes one PbI₂ per KI. The equation gives 1 PbI₂ : 2 KI, and only the mole ratio switches substances.
Inverting the ratio. (2 mol KI / 1 mol PbI₂) leaves mol KI uncancelled, and 0.0450 × 2 × 461.0 = 41.5 g is wrong. Write the wanted substance on top, so the given unit cancels.
Dr. Karmach

Practice 1

FeCl₃ + 3 NaOH → Fe(OH)₃ + 3 NaCl
molar mass Fe(OH)₃ 106.87 g/mol

300.0 mL of 0.200 M NaOH reacts completely with excess iron(III) chloride, and rust-brown Fe(OH)₃ precipitates. What mass of Fe(OH)₃ forms?

  1. 2.14 g
  2. 6.41 g
  3. 19.2 g
  4. 2140 g
Dr. Karmach

Practice 1 — answer: A

FeCl₃ + 3 NaOH → Fe(OH)₃ + 3 NaCl
given: 300.0 mL of 0.200 M NaOH · wanted: g Fe(OH)₃ (106.87 g/mol)
0.3000 L soln × 0.200 mol NaOH1 L soln × 1 mol Fe(OH)₃3 mol NaOH × 106.87 g Fe(OH)₃1 mol Fe(OH)₃ = 2.14 g Fe(OH)₃ — answer A

B skipped the mole ratio: 0.0600 × 106.87 = 6.41. C inverted the ratio: 0.0600 × 3 × 106.87 = 19.2. D fed milliliters to the molarity: 300.0 × 0.200 = 60.0, a mole count 1000 times too large, and the chain ends at 2140 g.

0.0600 mol NaOH gives a third as many moles of Fe(OH)₃: 0.0200 mol, at about 107 g per mole — about 2 g. 2.14 g ✓
Dr. Karmach

Worked example 3 — volume of a second solution

H₂SO₄ + 2 NaOH → Na₂SO₄ + 2 H₂O
given: 175.0 mL of 0.240 M NaOH · wanted: mL of 0.150 M H₂SO₄

A base spill of 175.0 mL of 0.240 M NaOH is neutralized with 0.150 M H₂SO₄ from the shelf. What volume of the acid solution, in milliliters, reacts completely?

Count the factors on the route: mL → L → mol NaOH → mol H₂SO₄ → L → mL.

Dr. Karmach

Worked example 3 — solution

H₂SO₄ + 2 NaOH → Na₂SO₄ + 2 H₂O

Three conversion factors are needed. Molarity works at both ends: the base's converts volume in to moles, the acid's converts moles out to volume.

Step 1 · Volume → moles

175.0 mL is 0.1750 L. The base's molarity converts the liters to moles of NaOH:

0.1750 L NaOH soln × 0.240 mol NaOH1 L NaOH soln = 0.0420 mol NaOH
Dr. Karmach

Worked example 3 — solution

H₂SO₄ + 2 NaOH → Na₂SO₄ + 2 H₂O
Step 1 · Volume → moles
0.1750 L NaOH soln × 0.240 mol NaOH1 L NaOH soln = 0.0420 mol NaOH
Step 2 · Moles → moles

The mole ratio, written H₂SO₄ over NaOH (1 : 2), gives 0.0210 mol H₂SO₄.

Dr. Karmach

Worked example 3 — solution

H₂SO₄ + 2 NaOH → Na₂SO₄ + 2 H₂O
Step 1 · Volume → moles
0.1750 L NaOH soln × 0.240 mol NaOH1 L NaOH soln = 0.0420 mol NaOH
Step 2 · Moles → moles Step 3 · Moles → the wanted unit

The acid's molarity converts moles out to volume:

0.1750 L NaOH soln × 0.240 mol NaOH1 L NaOH soln × 1 mol H₂SO₄2 mol NaOH × 1 L acid soln0.150 mol H₂SO₄ = 0.140 L = 140. mL acid soln
Dr. Karmach

Worked example 3 — solution

H₂SO₄ + 2 NaOH → Na₂SO₄ + 2 H₂O
Step 1 · Volume → moles
0.1750 L NaOH soln × 0.240 mol NaOH1 L NaOH soln = 0.0420 mol NaOH
Step 2 · Moles → moles Step 3 · Moles → the wanted unit
0.1750 L NaOH soln × 0.240 mol NaOH1 L NaOH soln × 1 mol H₂SO₄2 mol NaOH × 1 L acid soln0.150 mol H₂SO₄ = 0.140 L = 140. mL acid soln
Half the moles (0.0210 vs 0.0420), but fewer per liter (0.150 vs 0.240): 140. mL is near 175.0 mL ✓
Dr. Karmach

Practice 2

Ba(OH)₂ + 2 HCl → BaCl₂ + 2 H₂O
two labeled solutions: 0.250 M Ba(OH)₂ · 0.400 M HCl

150.0 mL of 0.250 M Ba(OH)₂ reacts completely with 0.400 M HCl. What volume of the HCl solution, in milliliters, is required?

  1. 30.0 mL
  2. 46.9 mL
  3. 93.8 mL
  4. 188 mL
Dr. Karmach

Practice 2 — answer: D

Ba(OH)₂ + 2 HCl → BaCl₂ + 2 H₂O
given: 150.0 mL of 0.250 M Ba(OH)₂ · wanted: mL of 0.400 M HCl
0.1500 L base soln × 0.250 mol Ba(OH)₂1 L base soln × 2 mol HCl1 mol Ba(OH)₂ × 1 L acid soln0.400 mol HCl = 0.1875 L = 188 mL — answer D

A flipped the acid's molarity factor: 0.0750 × 0.400 = 0.0300, and the units, mol²/L, are not a volume. B inverted the mole ratio: 0.0375 × 1/2 ÷ 0.400 = 0.0469 L, or 46.9 mL. C skipped the mole ratio: 0.0375 ÷ 0.400 = 0.0938 L, or 93.8 mL.

Two HCl are needed per Ba(OH)₂, and the acid is not twice as concentrated (0.400 vs 0.250 M), so the acid volume comes out larger: 188 mL vs 150.0 mL ✓
Dr. Karmach

Check yourself

  1. A bottle is labeled 2.00 M NaOH. Write the setup that converts 50.0 mL of this solution to moles of NaOH.
  2. In the route L of A → mol A → mol B → L of B, name the conversion factor at each arrow. Which one comes from the balanced equation?

This chain also runs backward: the volume of a known-molarity solution that reacts completely with an unknown gives the unknown's moles. That laboratory measurement is a titration.

Dr. Karmach

6 · Types of Reactions

Spot the evidence that a reaction occurred, classify any equation as one of the five reaction types, and predict products from the pattern.

Dr. Karmach

Signs of a new substance

Baking soda and vinegar foam. A nail turns brown and flaky. Stove gas burns blue. Each change makes a new substance, and each leaves a visible sign.

Dr. Karmach

Reactions repeat a few patterns

2 Na + Cl₂ → 2 NaCl
element + element → one compound
2 Mg + O₂ → 2 MgO
element + element → one compound — the same pattern

Millions of reactions are known. Nearly all follow a few repeating patterns, visible in the equation's shape. Recognizing the pattern tells what the products must be before any balancing starts.

Dr. Karmach

Evidence a reaction occurred

New substances have new properties, so the change is visible. Watch for a color change, a gas bubbling out, a solid settling from clear solutions (a precipitate), a temperature change, or light.

Dr. Karmach

The five patterns

The shape carries the classification: how many substances on each side, and whether each is an element or a compound. Combustion adds a signature: O₂ consumed, CO₂ and H₂O formed.

Dr. Karmach

The method

  1. Inventory each side. Count the substances; mark each as element or compound.
  2. Match the shape. Pick the pattern the inventory fits.
  3. Name the type and complete the products. If products are missing, the pattern supplies them.
Dr. Karmach

Worked example 1 — heating limestone

Step 1 · Inventory each side

CaCO₃(s) → CaO(s) + CO₂(g)
one reactant, a compound → two products, both compounds  ·  O: 3 = 1 + 2 ✓

Limestone breaks down in a hot kiln. Classify the reaction.

A common first attempt: CO₂ forms, so combustion. Test it.

Dr. Karmach

Worked example 1 — solution

CaCO₃(s) → CaO(s) + CO₂(g)
one reactant, a compound → two products, both compounds

A common first attempt

CaCO₃ → CaO + CO₂ as a combustion
combustion: fuel + O₂ → CO₂ + H₂O  ·  no O₂ is consumed here ✗

Nothing burns. Combustion consumes O₂ as a reactant, and no O₂ appears on the left.

Dr. Karmach

Worked example 1 — solution

CaCO₃(s) → CaO(s) + CO₂(g)
one reactant, a compound → two products, both compounds
A common first attempt
CaCO₃ → CaO + CO₂ as a combustion
combustion: fuel + O₂ → CO₂ + H₂O  ·  no O₂ is consumed here ✗
Step 2 · Match the shape

One reactant, two products. Only one pattern starts from a single substance: AB → A + B.

Dr. Karmach

Worked example 1 — solution

CaCO₃(s) → CaO(s) + CO₂(g)
one reactant, a compound → two products, both compounds
A common first attempt
CaCO₃ → CaO + CO₂ as a combustion
combustion: fuel + O₂ → CO₂ + H₂O  ·  no O₂ is consumed here ✗
Step 2 · Match the shape Step 3 · Name the type and complete the products
CaCO₃(s) → CaO(s) + CO₂(g) — decomposition
Ca: 1 = 1 ✓  ·  C: 1 = 1 ✓  ·  O: 3 = 1 + 2 ✓
Dr. Karmach

Worked example 1 — solution

CaCO₃(s) → CaO(s) + CO₂(g)
one reactant, a compound → two products, both compounds
A common first attempt
CaCO₃ → CaO + CO₂ as a combustion
combustion: fuel + O₂ → CO₂ + H₂O  ·  no O₂ is consumed here ✗
Step 2 · Match the shape Step 3 · Name the type and complete the products
CaCO₃(s) → CaO(s) + CO₂(g) — decomposition
Ca: 1 = 1 ✓  ·  C: 1 = 1 ✓  ·  O: 3 = 1 + 2 ✓
Heat split one compound into two simpler ones. CO₂ appeared without any burning: the products alone cannot name the type.
Dr. Karmach

Take-home: combustion is read from the reactants

CH₄ + 2 O₂ → CO₂ + 2 H₂O — combustion
O₂ consumed  ·  a fuel burned to CO₂ and H₂O
CaCO₃ → CaO + CO₂ — decomposition
CO₂ formed, but no O₂ consumed — one compound splitting

A product alone never classifies a reaction. Combustion needs O₂ on the reactant side; CO₂ among the products can come from burning or from breaking down.

Dr. Karmach

Worked example 2 — propane on a grill

Step 1 · Inventory each side

C₃H₈(g) + O₂(g) → ?
a carbon–hydrogen fuel + the element O₂  ·  products not yet written

Propane burns in a grill. Classify the reaction, write the products the pattern requires, and balance.

Dr. Karmach

Worked example 2 — solution

C₃H₈(g) + O₂(g) → ?
a carbon–hydrogen fuel + the element O₂

Step 2 · Match the shape

A fuel reacting with O₂ fits one pattern: combustion.

Dr. Karmach

Worked example 2 — solution

C₃H₈(g) + O₂(g) → ?
a carbon–hydrogen fuel + the element O₂
Step 2 · Match the shape Step 3 · Name the type and complete the products
C₃H₈ + O₂ → CO₂ + H₂O  (skeleton)
every C leaves in CO₂  ·  every H leaves in H₂O

The pattern fixes both products before any balancing. Balancing now assigns the coefficients: C first, H second, O last.

Dr. Karmach

Worked example 2 — solution

C₃H₈(g) + O₂(g) → ?
a carbon–hydrogen fuel + the element O₂
Step 2 · Match the shape Step 3 · Name the type and complete the products
C₃H₈ + O₂ → CO₂ + H₂O  (skeleton)
every C leaves in CO₂  ·  every H leaves in H₂O
The balance check
C₃H₈ + 5 O₂ → 3 CO₂ + 4 H₂O
C: 3 = 3 ✓  ·  H: 8 = 8 ✓  ·  O: 10 = 6 + 4 ✓
Dr. Karmach

Worked example 2 — solution

C₃H₈(g) + O₂(g) → ?
a carbon–hydrogen fuel + the element O₂
Step 2 · Match the shape Step 3 · Name the type and complete the products
C₃H₈ + O₂ → CO₂ + H₂O  (skeleton)
every C leaves in CO₂  ·  every H leaves in H₂O
The balance check
C₃H₈ + 5 O₂ → 3 CO₂ + 4 H₂O
C: 3 = 3 ✓  ·  H: 8 = 8 ✓  ·  O: 10 = 6 + 4 ✓
Every carbon–hydrogen fuel burns to the same two products. The pattern chose CO₂ and H₂O; balancing only chose the amounts.
Dr. Karmach

Your turn — magnesium in acid

Mg(s) + 2 HCl(aq) → MgCl₂(aq) + H₂(g)
bubbles rise as the metal dissolves  ·  H: 2 = 2 ✓  ·  Cl: 2 = 2 ✓
step question answer
1 · Inventory each side element or compound? bare element + compound → compound + bare
2 · Match the shape which pattern fits? A + BC → + B
3 · Name the type displacement

Complete the three steps.

Dr. Karmach

Your turn — magnesium in acid

Mg(s) + 2 HCl(aq) → MgCl₂(aq) + H₂(g)
bubbles rise as the metal dissolves  ·  H: 2 = 2 ✓  ·  Cl: 2 = 2 ✓
step question answer
1 · Inventory each side element or compound? bare element + compound → compound + bare
2 · Match the shape which pattern fits? A + BC → + B
3 · Name the type displacement

Complete the three steps.

Mg + 2 HCl → MgCl₂ + H₂ — single displacement
Mg displaces hydrogen from HCl  ·  the escaping H₂ gas is the visible evidence
Dr. Karmach

Where this goes wrong

Reading any two-and-two equation as a partner swap. Zn + CuSO₄ → ZnSO₄ + Cu shows two reactants and two products, but Zn enters as a bare element. Double displacement needs two compounds; a bare element displacing another is single displacement.
Calling every CO₂ producer combustion. CaCO₃ → CaO + CO₂ releases CO₂ with no O₂ consumed. Combustion consumes O₂ and forms CO₂ and H₂O; one compound splitting apart is decomposition.
Reading the arrow backwards. Combination builds one product from several reactants; decomposition splits one reactant into several products. 2 HgO → 2 Hg + O₂ starts from a single compound: decomposition.
Calling every bright, hot reaction combustion. 2 Na + Cl₂ → 2 NaCl gives off heat and light, yet no O₂ is consumed and no CO₂ or H₂O forms. Two elements forming one compound: combination.
Dr. Karmach

Practice 1

2 C₂H₂(g) + 5 O₂(g) → 4 CO₂(g) + 2 H₂O(g)
C: 4 = 4 ✓  ·  H: 4 = 4 ✓  ·  O: 10 = 8 + 2 ✓

A welding torch burns acetylene, C₂H₂, in pure oxygen. Which type best classifies this reaction?

  1. Double displacement — two reactants form two products, so two pairs traded partners
  2. Combination — the fuel and the oxygen combine into new compounds
  3. Combustion — a carbon–hydrogen fuel consumes O₂ and forms CO₂ and H₂O
  4. Decomposition — the heat breaks the C₂H₂ molecule apart
Dr. Karmach

Practice 1 — answer: C

2 C₂H₂ + 5 O₂ → 4 CO₂ + 2 H₂O — combustion — answer C
a carbon–hydrogen fuel consumes O₂ and forms CO₂ and H₂O — the full signature

A: a partner swap needs two compounds trading ions, and O₂ is a bare element. B: combination merges everything into one product; two products form here. D: decomposition starts from one reactant; two react here, and the fuel is not falling apart on its own.

Fuel and O₂ on the left, CO₂ and H₂O on the right. The same signature classifies every burning hydrocarbon.
Dr. Karmach

Worked example 3 — single or double displacement

Step 1 · Inventory each side

Zn(s) + CuSO₄(aq) → ZnSO₄(aq) + Cu(s)
bare element + compound → compound + bare element
AgNO₃(aq) + KCl(aq) → AgCl(s) + KNO₃(aq)
compound + compound → compound + compound — no bare element

Each equation shows two reactants and two products. Classify each reaction.

Dr. Karmach

Worked example 3 — match the shape

Zn + CuSO₄ → ZnSO₄ + Cu
bare element + compound → compound + bare element
AgNO₃ + KCl → AgCl + KNO₃
compound + compound → compound + compound

Step 2 · Match the shape

Counting substances cannot separate these: both show two reactants and two products. The inventory can: the first equation carries a bare element, the second carries none.

Dr. Karmach

Worked example 3 — match the shape

Zn + CuSO₄ → ZnSO₄ + Cu
bare element + compound → compound + bare element
AgNO₃ + KCl → AgCl + KNO₃
compound + compound → compound + compound

Step 2 · Match the shape

Counting substances cannot separate these: both show two reactants and two products. The inventory can: the first equation carries a bare element, the second carries none.
The first fits A + BC → AC + B. The second fits AB + CD → AD + CB.

Substance counts match pattern to pattern. The element-or-compound inventory is what tells the two displacements apart.
Dr. Karmach

Worked example 3 — name the types

Step 3 · Name the type and complete the products

Zn + CuSO₄ → ZnSO₄ + Cu — single displacement
A + BC → AC + B  ·  Zn displaces Cu; copper leaves as the bare element
Dr. Karmach

Worked example 3 — name the types

Step 3 · Name the type and complete the products

Zn + CuSO₄ → ZnSO₄ + Cu — single displacement
A + BC → AC + B  ·  Zn displaces Cu; copper leaves as the bare element
AgNO₃ + KCl → AgCl + KNO₃ — double displacement
AB + CD → AD + CB  ·  the compounds trade partners; AgCl is a precipitate
Dr. Karmach

Worked example 3 — name the types

Step 3 · Name the type and complete the products

Zn + CuSO₄ → ZnSO₄ + Cu — single displacement
A + BC → AC + B  ·  Zn displaces Cu; copper leaves as the bare element
AgNO₃ + KCl → AgCl + KNO₃ — double displacement
AB + CD → AD + CB  ·  the compounds trade partners; AgCl is a precipitate
A bare element among the reactants marks single displacement. Two compounds trading partners, with no bare element anywhere, marks double displacement.
Dr. Karmach

Practice 2

Ba(NO₃)₂(aq) + K₂SO₄(aq) → BaSO₄(s) + 2 KNO₃(aq)
two clear solutions mixed — a white solid settles out

Barium nitrate and potassium sulfate solutions are mixed, and a white solid appears. Which type best classifies this reaction?

  1. Single displacement — barium displaces potassium from its compound
  2. Combination — the two reactants combine into the one solid product
  3. Decomposition — a compound broke down, which is why a solid fell out
  4. Double displacement — two compounds trade partners, and one new pair leaves as a solid
Dr. Karmach

Practice 2 — answer: D

Ba(NO₃)₂ + K₂SO₄ → BaSO₄ + 2 KNO₃ — double displacement — answer D
AB + CD → AD + CB  ·  the new pair BaSO₄ is the precipitate — the visible evidence

A: single displacement needs a bare element among the reactants, and every substance here is a compound. B: combination ends in one product; two form, and KNO₃ stays dissolved. C: decomposition starts from one reactant; two were mixed, and nothing split into simpler substances.

Two compounds in, two compounds out, one of them insoluble. The white solid is the evidence that the partners traded.
Dr. Karmach

Check yourself

  1. Hydrogen peroxide slowly turns into water and oxygen: 2 H₂O₂ → 2 H₂O + O₂. Inventory each side and name the type. O₂ and H₂O both appear — why is this not combustion?
  2. Butane, C₄H₁₀, burns in a lighter. Write the two products before balancing anything. Which pattern makes that prediction possible?

A double displacement happens only when a new pair leaves the solution — as a solid, a gas, or water. The solubility rules predict which ion pairs drop out as precipitates.

Dr. Karmach

7 · Solubility Rules & Precipitation

Predict whether mixing two solutions makes a precipitate — swap the partners, check each new compound against the solubility rules, and write the balanced equation with states.

Dr. Karmach

A solid from two clear liquids

Two beakers, two clear liquids. Poured together, they instantly cloud, and a bright yellow solid settles to the bottom. No solid went in.

Dr. Karmach

Soluble or insoluble

NaCl(aq) — soluble: it dissolves, and its ions spread through the water
(aq) = aqueous, dissolved in water
AgCl(s) — insoluble: it stays a solid
(s) = solid — it does not dissolve

An ionic compound in water either dissolves or it does not. Which way each compound goes is a fixed fact, set by a short list of rules.

Dr. Karmach

The solubility rules

One line decides each compound: read its ions, find their line, apply the exception list.

Dr. Karmach

Mixing two solutions: the partners swap

Dissolved compounds are separated ions. Mixing two solutions lets each cation meet the other anion. A new pairing the rules call insoluble forms a solid: a precipitate.

Dr. Karmach

The method

  1. Swap the partners. New cation–anion pairs.
  2. Build each new formula. Charge balance sets subscripts.
  3. Check each product against the rules. Soluble → (aq); insoluble → (s).
  4. Write the balanced equation with states. Both products (aq): no reaction.
Dr. Karmach

Worked example 1 — soluble or insoluble

CaCO₃ · K₂CO₃
wanted: the state of each in water — (aq) or (s)

Marble is CaCO₃. Potash fertilizer, K₂CO₃, is spread as a solution. Assign each compound its state in water.

Dr. Karmach

Worked example 1 — solution

CaCO₃ · K₂CO₃
wanted: the state of each in water — (aq) or (s)

Read the ions

CaCO₃ = Ca²⁺ + CO₃²⁻ · K₂CO₃ = 2 K⁺ + CO₃²⁻
both compounds are carbonates — the carbonate line decides both
Dr. Karmach

Worked example 1 — solution

CaCO₃ · K₂CO₃
wanted: the state of each in water — (aq) or (s)
Read the ions
CaCO₃ = Ca²⁺ + CO₃²⁻ · K₂CO₃ = 2 K⁺ + CO₃²⁻
both compounds are carbonates — the carbonate line decides both
Apply the carbonate line

Carbonates are insoluble except with group 1 cations or NH₄⁺.

CaCO₃ → CaCO₃(s) · K₂CO₃ → K₂CO₃(aq)
Ca²⁺: not on the exception list → solid · K⁺: group 1 → the exception applies, dissolved
Dr. Karmach

Worked example 1 — solution

CaCO₃ · K₂CO₃
wanted: the state of each in water — (aq) or (s)
Read the ions
CaCO₃ = Ca²⁺ + CO₃²⁻ · K₂CO₃ = 2 K⁺ + CO₃²⁻
both compounds are carbonates — the carbonate line decides both
Apply the carbonate line

Carbonates are insoluble except with group 1 cations or NH₄⁺.

CaCO₃ → CaCO₃(s) · K₂CO₃ → K₂CO₃(aq)
Ca²⁺: not on the exception list → solid · K⁺: group 1 → the exception applies, dissolved
Same anion, opposite states. A rule reads the pair of ions; the exception list is part of the rule.
Dr. Karmach

Worked example 2 — AgNO₃ + NaCl

AgNO₃(aq) + NaCl(aq) → ?
wanted: the precipitate

Silver nitrate solution meets salt solution in photographic processing. Both are clear; mixing them turns the beaker milky white. Predict the solid.

A common first attempt: check AgNO₃ and NaCl against the rules — both soluble, so no solid should form. Test it.

Dr. Karmach

Worked example 2 — testing the first attempt

AgNO₃(aq) + NaCl(aq) → ?
wanted: the precipitate

A common first attempt

AgNO₃ soluble ✓ · NaCl soluble ✓ → no solid?
nitrates: always soluble · group 1: always soluble — yet the mixture turns white ✗
Dr. Karmach

Worked example 2 — testing the first attempt

AgNO₃(aq) + NaCl(aq) → ?
wanted: the precipitate

A common first attempt

AgNO₃ soluble ✓ · NaCl soluble ✓ → no solid?
nitrates: always soluble · group 1: always soluble — yet the mixture turns white ✗
Both reactants pass the rules. That is what (aq) already records: they arrived dissolved. The white solid must be a compound neither beaker held.
The mixed beaker holds four ions moving independently: Ag⁺, NO₃⁻, Na⁺, Cl⁻. Two of them meet here for the first time.
Dr. Karmach

Worked example 2 — the swap

AgNO₃(aq) + NaCl(aq) → ?
wanted: the precipitate

Step 1 · Swap the partners Step 2 · Build each new formula

Ag⁺ pairs with Cl⁻; Na⁺ pairs with NO₃⁻. Both new pairs balance one-to-one.

Dr. Karmach

Worked example 2 — the swap

AgNO₃(aq) + NaCl(aq) → ?
wanted: the precipitate

Step 1 · Swap the partners Step 2 · Build each new formula

Ag⁺ pairs with Cl⁻; Na⁺ pairs with NO₃⁻. Both new pairs balance one-to-one.

new pairs: AgCl and NaNO₃
AgCl: 1(+1) + 1(−1) = 0 ✓ · NaNO₃: 1(+1) + 1(−1) = 0 ✓
Two dissolved compounds went in; two new pairings remain to be checked against the rules.
Dr. Karmach

Worked example 2 — states and the equation

AgNO₃(aq) + NaCl(aq) → AgCl + NaNO₃
new pairs built — wanted: each product's state

Step 3 · Check each product against the rules

AgCl → (s) · NaNO₃ → (aq)
chlorides: soluble except Ag⁺, Pb²⁺, Hg₂²⁺ — Ag⁺ is on the list · nitrates: always soluble
Dr. Karmach

Worked example 2 — states and the equation

AgNO₃(aq) + NaCl(aq) → AgCl + NaNO₃
new pairs built — wanted: each product's state
Step 3 · Check each product against the rules
AgCl → (s) · NaNO₃ → (aq)
chlorides: soluble except Ag⁺, Pb²⁺, Hg₂²⁺ — Ag⁺ is on the list · nitrates: always soluble
Step 4 · Write the balanced equation with states
AgNO₃(aq) + NaCl(aq) → AgCl(s) + NaNO₃(aq)
Ag: 1 = 1 · NO₃: 1 = 1 · Na: 1 = 1 · Cl: 1 = 1 — balanced as written
Dr. Karmach

Worked example 2 — states and the equation

AgNO₃(aq) + NaCl(aq) → AgCl + NaNO₃
new pairs built — wanted: each product's state
Step 3 · Check each product against the rules
AgCl → (s) · NaNO₃ → (aq)
chlorides: soluble except Ag⁺, Pb²⁺, Hg₂²⁺ — Ag⁺ is on the list · nitrates: always soluble
Step 4 · Write the balanced equation with states
AgNO₃(aq) + NaCl(aq) → AgCl(s) + NaNO₃(aq)
Ag: 1 = 1 · NO₃: 1 = 1 · Na: 1 = 1 · Cl: 1 = 1 — balanced as written
The milky white is AgCl, the one new pairing the rules call insoluble. Na⁺ and NO₃⁻ never left the water.
Dr. Karmach

Take-home: apply the rules to the products

AgNO₃(aq) + NaCl(aq) — reactants already dissolved
(aq) on a reactant records that it already dissolved
Ag⁺ + Cl⁻ → AgCl(s) — the new pairing
chlorides: soluble except Ag⁺, Pb²⁺, Hg₂²⁺

Swap first, then check. The precipitate question is about the two new pairings, never about the compounds that arrived dissolved.

Dr. Karmach

Your turn — Pb(NO₃)₂ + KI

Pb(NO₃)₂(aq) + KI(aq) → ?
two clear solutions · mixing makes a bright yellow solid
step question answer
1 · swap the partners which new pairs form? Pb²⁺ with I⁻ · K⁺ with NO₃⁻
2 · build each new formula 1(+2) + 2(−1) = 0 PbI and KNO₃
3 · check each product which lines of the rules? PbI₂ → () · KNO₃ → ()
4 · write the balanced equation coefficients

Complete the prediction.

Dr. Karmach

Your turn — Pb(NO₃)₂ + KI

Pb(NO₃)₂(aq) + KI(aq) → ?
two clear solutions · mixing makes a bright yellow solid
step question answer
1 · swap the partners which new pairs form? Pb²⁺ with I⁻ · K⁺ with NO₃⁻
2 · build each new formula 1(+2) + 2(−1) = 0 PbI and KNO₃
3 · check each product which lines of the rules? PbI₂ → () · KNO₃ → ()
4 · write the balanced equation coefficients

Complete the prediction.

Pb(NO₃)₂(aq) + 2 KI(aq) → PbI₂(s) + 2 KNO₃(aq)
PbI₂: 1(+2) + 2(−1) = 0 ✓ · iodides: soluble except Ag⁺, Pb²⁺, Hg₂²⁺ · nitrates: always soluble
Dr. Karmach

Where this goes wrong

Checking the rules on the starting solutions. AgNO₃ and NaCl both pass — they were already dissolved. The rules judge the products of the swap: Ag⁺ with Cl⁻ gives AgCl, and the chloride line puts Ag⁺ on its exception list.
Calling the soluble product the precipitate. BaCl₂ + Na₂SO₄ gives two new pairs. NaCl passes the rules, so its ions stay dissolved. The solid is the pairing that does not: BaSO₄.
Expecting a starting compound to fall out. A compound that arrived dissolved stays dissolved. The precipitate is always a new pairing — ions that arrived in different beakers.
Dragging old subscripts into new formulas. Pb(NO₃)₂ + KI: copying KI's one-to-one ratio gives PbI, and 1(+2) + 1(−1) = +1, not neutral. Charge balance builds the new formula: PbI₂, 1(+2) + 2(−1) = 0.
Dr. Karmach

Practice 1

Ba(NO₃)₂(aq) + K₂SO₄(aq) → ?
two clear solutions are mixed

Solutions of barium nitrate and potassium sulfate are mixed. Which precipitate forms, if any?

  1. KNO₃
  2. BaSO₄
  3. Ba(NO₃)₂
  4. No precipitate — both new pairings stay dissolved
Dr. Karmach

Practice 1 — answer: B

Ba(NO₃)₂(aq) + K₂SO₄(aq) → BaSO₄(s) + 2 KNO₃(aq) — answer B
sulfates: soluble except Ba²⁺, Sr²⁺, Pb²⁺ · Ba: 1 = 1 · SO₄: 1 = 1 · K: 2 = 2 · NO₃: 2 = 2

A is the soluble product: potassium is group 1 and nitrate is always soluble, so KNO₃'s ions stay dissolved. C is a reactant: Ba(NO₃)₂ arrived dissolved, and a dissolved compound does not leave solution when another is added. D skipped the check on BaSO₄ — barium is on the sulfate exception list.

Of the four ions mixed, only the Ba²⁺ + SO₄²⁻ pairing appears on an exception list. One insoluble pairing, one solid.
Dr. Karmach

Worked example 3 — BaCl₂ + NaOH

BaCl₂(aq) + NaOH(aq) → ?
wanted: the precipitate, if one forms

Solutions of barium chloride and sodium hydroxide are mixed. Work all four steps.

Dr. Karmach

Worked example 3 — the swap

BaCl₂(aq) + NaOH(aq) → ?
wanted: the precipitate, if one forms

Step 1 · Swap the partners Step 2 · Build each new formula

Ba²⁺ pairs with OH⁻; Na⁺ pairs with Cl⁻. Ba²⁺ needs two OH⁻ to reach zero charge.

Dr. Karmach

Worked example 3 — the swap

BaCl₂(aq) + NaOH(aq) → ?
wanted: the precipitate, if one forms

Step 1 · Swap the partners Step 2 · Build each new formula

Ba²⁺ pairs with OH⁻; Na⁺ pairs with Cl⁻. Ba²⁺ needs two OH⁻ to reach zero charge.

new pairs: Ba(OH)₂ and NaCl
Ba(OH)₂: 1(+2) + 2(−1) = 0 ✓ · NaCl: 1(+1) + 1(−1) = 0 ✓
The new formulas come from charge balance, never from the reactants' subscripts.
Dr. Karmach

Worked example 3 — solution

BaCl₂(aq) + NaOH(aq) → Ba(OH)₂ + NaCl
new pairs built — wanted: each product's state

Step 3 · Check each product against the rules

Most hydroxides are insoluble. The exception list is part of the rule, and Ba²⁺ is on it.

Ba(OH)₂ → (aq) · NaCl → (aq)
hydroxides: insoluble except group 1 and Ba²⁺ · group 1: always soluble
Dr. Karmach

Worked example 3 — solution

BaCl₂(aq) + NaOH(aq) → Ba(OH)₂ + NaCl
new pairs built — wanted: each product's state
Step 3 · Check each product against the rules
Ba(OH)₂ → (aq) · NaCl → (aq)
hydroxides: insoluble except group 1 and Ba²⁺ · group 1: always soluble
Step 4 · Write the balanced equation with states
BaCl₂(aq) + NaOH(aq) → no reaction
both new pairings stay dissolved — nothing leaves the solution
Dr. Karmach

Worked example 3 — solution

BaCl₂(aq) + NaOH(aq) → Ba(OH)₂ + NaCl
new pairs built — wanted: each product's state
Step 3 · Check each product against the rules
Ba(OH)₂ → (aq) · NaCl → (aq)
hydroxides: insoluble except group 1 and Ba²⁺ · group 1: always soluble
Step 4 · Write the balanced equation with states
BaCl₂(aq) + NaOH(aq) → no reaction
both new pairings stay dissolved — nothing leaves the solution
The mixed beaker stays clear: it holds four kinds of dissolved ions. A precipitate needs one insoluble pairing, and here there is none.
Dr. Karmach

Practice 2

MgSO₄(aq) + NaCl(aq) → ?
two clear solutions are mixed

Epsom salt is MgSO₄; table salt is NaCl. Solutions of the two are mixed. Which precipitate forms, if any?

  1. MgCl₂
  2. Na₂SO₄
  3. No precipitate — both new pairings stay dissolved
  4. MgSO₄
Dr. Karmach

Practice 2 — answer: C

new pairs: MgCl₂ → (aq) · Na₂SO₄ → (aq) → no reaction — answer C
MgCl₂: 1(+2) + 2(−1) = 0 ✓ · Na₂SO₄: 2(+1) + 1(−2) = 0 ✓ · neither pairing is on an exception list

A: chlorides are soluble except with Ag⁺, Pb²⁺, Hg₂²⁺, and Mg²⁺ is not among them, so MgCl₂ stays dissolved. B: sodium is group 1, and group 1 compounds are always soluble. D is a reactant: MgSO₄ arrived dissolved, and no new pairing removed its ions.

Sulfates fail only with Ba²⁺, Sr²⁺, Pb²⁺. Four ions went in; four ions stay dissolved. The result is one mixed solution.
Dr. Karmach

Check yourself

  1. Solutions of Pb(NO₃)₂ and Na₂SO₄ are mixed. Swap the partners, build both formulas, check each against the rules: which product is the solid?
  2. Solutions of KCl and NH₄NO₃ are mixed. Both new pairings pass the rules. What is the prediction, and why?

Every (aq) compound in a precipitate equation is really separated ions in the water. Writing the dissolved compounds as their ions, then removing the ions that never change, leaves the net ionic equation — the precipitate-forming ions alone.

Dr. Karmach

8 · Net Ionic Equations

Write the molecular, complete ionic, and net ionic equations for a reaction in solution, cancel the spectator ions, and check that the result balances in atoms and charge.

Dr. Karmach

The solid takes only two kinds of particles

Two clear solutions are mixed; a white solid settles. Most dissolved particles are still floating afterward, unchanged. Only two kinds left the water.

Dr. Karmach

Dissolved means separated into ions

A soluble ionic compound does not dissolve as molecules. It exists in the water as separated ions, each moving on its own. Writing the ions shows which of them react and which never change.

Dr. Karmach

Three views of the same reaction

The molecular equation lists whole compounds. The two ionic views show what the water actually holds. All three keep the states and stay balanced.

Dr. Karmach

Spectator ions

Ag⁺(aq) + NO₃⁻(aq) + Na⁺(aq) + Cl⁻(aq) → AgCl(s) + Na⁺(aq) + NO₃⁻(aq)
Na⁺ and NO₃⁻ — dissolved before, dissolved after, unchanged

A spectator ion appears identical on both sides of the complete ionic equation. Cancel the spectators from both sides. What remains is the net ionic equation.

Dr. Karmach

The method

  1. Write the molecular equation with states.
  2. Write each (aq) compound as its ions. Keep charges and coefficients; polyatomic ions stay whole; (s) stays intact.
  3. Cancel the spectator ions.
  4. Check atoms and charge. Both must balance.
Dr. Karmach

Worked example 1 — silver chloride

Step 1 · Write the molecular equation with states

AgNO₃(aq) + NaCl(aq) → AgCl(s) + NaNO₃(aq)
states from the solubility rules — AgCl insoluble, the rest soluble

A drop of silver nitrate turns salty water cloudy white, a standard test for chloride. Write the complete ionic equation, then the net ionic equation.

Dr. Karmach

Worked example 1 — the complete ionic equation

AgNO₃(aq) + NaCl(aq) → AgCl(s) + NaNO₃(aq)
molecular — states from the solubility rules

Step 2 · Write each (aq) compound as its ions

Each (aq) compound separates. The solid does not.

Ag⁺(aq) + NO₃⁻(aq) + Na⁺(aq) + Cl⁻(aq) → AgCl(s) + Na⁺(aq) + NO₃⁻(aq)
complete ionic · charge: left 1(+1) + 1(−1) + 1(+1) + 1(−1) = 0 · right 0 + 1(+1) + 1(−1) = 0 ✓
Dr. Karmach

Worked example 1 — the complete ionic equation

AgNO₃(aq) + NaCl(aq) → AgCl(s) + NaNO₃(aq)
molecular — states from the solubility rules
Step 2 · Write each (aq) compound as its ions
Ag⁺(aq) + NO₃⁻(aq) + Na⁺(aq) + Cl⁻(aq) → AgCl(s) + Na⁺(aq) + NO₃⁻(aq)
complete ionic · charge: left 1(+1) + 1(−1) + 1(+1) + 1(−1) = 0 · right 0 + 1(+1) + 1(−1) = 0 ✓
Step 3 · Cancel the spectator ions

Na⁺ and NO₃⁻ appear identical on both sides. They never reacted.

Ag⁺(aq) + NO₃⁻(aq) + Na⁺(aq) + Cl⁻(aq) → AgCl(s) + Na⁺(aq) + NO₃⁻(aq)
spectators: Na⁺ and NO₃⁻
Dr. Karmach

Worked example 1 — the complete ionic equation

AgNO₃(aq) + NaCl(aq) → AgCl(s) + NaNO₃(aq)
molecular — states from the solubility rules
Step 2 · Write each (aq) compound as its ions
Ag⁺(aq) + NO₃⁻(aq) + Na⁺(aq) + Cl⁻(aq) → AgCl(s) + Na⁺(aq) + NO₃⁻(aq)
complete ionic · charge: left 1(+1) + 1(−1) + 1(+1) + 1(−1) = 0 · right 0 + 1(+1) + 1(−1) = 0 ✓
Step 3 · Cancel the spectator ions
Ag⁺(aq) + NO₃⁻(aq) + Na⁺(aq) + Cl⁻(aq) → AgCl(s) + Na⁺(aq) + NO₃⁻(aq)
spectators: Na⁺ and NO₃⁻
The compound formulas are gone; the water's actual contents are on the page, and the two ions that never react are struck out.
Dr. Karmach

Worked example 1 — the net ionic equation

AgNO₃(aq) + NaCl(aq) → AgCl(s) + NaNO₃(aq)
molecular · spectators already cancelled: Na⁺ and NO₃⁻

Step 4 · Check atoms and charge

Only the ions that build the solid remain.

Ag⁺(aq) + Cl⁻(aq) → AgCl(s)
net ionic · atoms: Ag 1 = 1 ✓ · Cl 1 = 1 ✓ · charge: left 1(+1) + 1(−1) = 0, right 0 ✓
Dr. Karmach

Worked example 1 — the net ionic equation

AgNO₃(aq) + NaCl(aq) → AgCl(s) + NaNO₃(aq)
molecular · spectators already cancelled: Na⁺ and NO₃⁻
Step 4 · Check atoms and charge
Ag⁺(aq) + Cl⁻(aq) → AgCl(s)
net ionic · atoms: Ag 1 = 1 ✓ · Cl 1 = 1 ✓ · charge: left 1(+1) + 1(−1) = 0, right 0 ✓
The net ionic equation balances twice: every atom matches, and both sides carry zero total charge.
Dr. Karmach

Worked example 2 — lead iodide

Step 1 · Write the molecular equation with states

Pb(NO₃)₂(aq) + 2 KI(aq) → PbI₂(s) + 2 KNO₃(aq)
PbI₂ insoluble — the yellow solid of the golden-rain demonstration

Write the complete ionic equation, then the net ionic equation.

A common first attempt for the net: Pb²⁺(aq) + I⁻(aq) → PbI₂(s). Test it.

Dr. Karmach

Worked example 2 — the complete ionic equation

Pb(NO₃)₂(aq) + 2 KI(aq) → PbI₂(s) + 2 KNO₃(aq)
molecular — PbI₂ is the solid

Step 2 · Write each (aq) compound as its ions

Pb(NO₃)₂ separates into one Pb²⁺ and two whole NO₃⁻. The coefficient on 2 KI carries through: 2 K⁺ and 2 I⁻.

Pb²⁺(aq) + 2 NO₃⁻(aq) + 2 K⁺(aq) + 2 I⁻(aq) → PbI₂(s) + 2 K⁺(aq) + 2 NO₃⁻(aq)
charge: left 1(+2) + 2(−1) + 2(+1) + 2(−1) = 0 · right 0 + 2(+1) + 2(−1) = 0 ✓
Dr. Karmach

Worked example 2 — the complete ionic equation

Pb(NO₃)₂(aq) + 2 KI(aq) → PbI₂(s) + 2 KNO₃(aq)
molecular — PbI₂ is the solid
Step 2 · Write each (aq) compound as its ions
Pb²⁺(aq) + 2 NO₃⁻(aq) + 2 K⁺(aq) + 2 I⁻(aq) → PbI₂(s) + 2 K⁺(aq) + 2 NO₃⁻(aq)
charge: left 1(+2) + 2(−1) + 2(+1) + 2(−1) = 0 · right 0 + 2(+1) + 2(−1) = 0 ✓
Step 3 · Cancel the spectator ions
Pb²⁺(aq) + 2 NO₃⁻(aq) + 2 K⁺(aq) + 2 I⁻(aq) → PbI₂(s) + 2 K⁺(aq) + 2 NO₃⁻(aq)
spectators: K⁺ and NO₃⁻ · Pb²⁺ and 2 I⁻ have no match to cancel
Dr. Karmach

Worked example 2 — the complete ionic equation

Pb(NO₃)₂(aq) + 2 KI(aq) → PbI₂(s) + 2 KNO₃(aq)
molecular — PbI₂ is the solid
Step 2 · Write each (aq) compound as its ions
Pb²⁺(aq) + 2 NO₃⁻(aq) + 2 K⁺(aq) + 2 I⁻(aq) → PbI₂(s) + 2 K⁺(aq) + 2 NO₃⁻(aq)
charge: left 1(+2) + 2(−1) + 2(+1) + 2(−1) = 0 · right 0 + 2(+1) + 2(−1) = 0 ✓
Step 3 · Cancel the spectator ions
Pb²⁺(aq) + 2 NO₃⁻(aq) + 2 K⁺(aq) + 2 I⁻(aq) → PbI₂(s) + 2 K⁺(aq) + 2 NO₃⁻(aq)
spectators: K⁺ and NO₃⁻ · Pb²⁺ and 2 I⁻ have no match to cancel
Nitrate separates and cancels as one whole unit, never as N and O pieces, and its coefficient 2 stays with it.
Dr. Karmach

Worked example 2 — the net ionic equation

Pb(NO₃)₂(aq) + 2 KI(aq) → PbI₂(s) + 2 KNO₃(aq)
molecular · spectators already cancelled: K⁺ and NO₃⁻

A common first attempt

Pb²⁺(aq) + I⁻(aq) → PbI₂(s)
atoms: I 1 ≠ 2 ✗ · charge: left 1(+2) + 1(−1) = +1, right 0 ✗

The coefficient on I⁻ was dropped. Two iodides build each PbI₂.

Dr. Karmach

Worked example 2 — the net ionic equation

Pb(NO₃)₂(aq) + 2 KI(aq) → PbI₂(s) + 2 KNO₃(aq)
molecular · spectators already cancelled: K⁺ and NO₃⁻
A common first attempt
Pb²⁺(aq) + I⁻(aq) → PbI₂(s)
atoms: I 1 ≠ 2 ✗ · charge: left 1(+2) + 1(−1) = +1, right 0 ✗
Step 4 · Check atoms and charge
Pb²⁺(aq) + 2 I⁻(aq) → PbI₂(s)
atoms: Pb 1 = 1 ✓ · I 2 = 2 ✓ · charge: left 1(+2) + 2(−1) = 0, right 0 ✓
Dr. Karmach

Worked example 2 — the net ionic equation

Pb(NO₃)₂(aq) + 2 KI(aq) → PbI₂(s) + 2 KNO₃(aq)
molecular · spectators already cancelled: K⁺ and NO₃⁻
A common first attempt
Pb²⁺(aq) + I⁻(aq) → PbI₂(s)
atoms: I 1 ≠ 2 ✗ · charge: left 1(+2) + 1(−1) = +1, right 0 ✗
Step 4 · Check atoms and charge
Pb²⁺(aq) + 2 I⁻(aq) → PbI₂(s)
atoms: Pb 1 = 1 ✓ · I 2 = 2 ✓ · charge: left 1(+2) + 2(−1) = 0, right 0 ✓
The solid is neutral, so the ions that build it must sum to zero. Keeping the coefficients is what makes both checks pass.
Dr. Karmach

Take-home: balance atoms and charge

Pb²⁺(aq) + 2 I⁻(aq) → PbI₂(s)
atoms: Pb 1 = 1 ✓ · I 2 = 2 ✓ · charge: 0 = 0 ✓
Pb²⁺(aq) + I⁻(aq) → PbI₂(s)
atoms: I 1 ≠ 2 ✗ · charge: +1 ≠ 0 ✗

Check atoms and total charge on both sides. An equation that fails either check is wrong.

Dr. Karmach

Your turn — barium sulfate

BaCl₂(aq) + Na₂SO₄(aq) → BaSO₄(s) + 2 NaCl(aq)
Step 1 done · BaSO₄ insoluble — the X-ray contrast a patient drinks
step your work
2 · write each (aq) compound as its ions Ba²⁺ + 2 Cl⁻ + 2 Na⁺ + → BaSO₄(s) + 2 Na⁺ + 2 Cl⁻
3 · cancel the spectator ions and
4 · check atoms and charge net: · left charge = right charge 0

Complete steps 2 through 4.

Dr. Karmach

Your turn — barium sulfate

BaCl₂(aq) + Na₂SO₄(aq) → BaSO₄(s) + 2 NaCl(aq)
Step 1 done · BaSO₄ insoluble — the X-ray contrast a patient drinks
step your work
2 · write each (aq) compound as its ions Ba²⁺ + 2 Cl⁻ + 2 Na⁺ + → BaSO₄(s) + 2 Na⁺ + 2 Cl⁻
3 · cancel the spectator ions and
4 · check atoms and charge net: · left charge = right charge 0

Complete steps 2 through 4.

Ba²⁺(aq) + SO₄²⁻(aq) → BaSO₄(s)
spectators: Na⁺, Cl⁻ · atoms: Ba 1 = 1 ✓ · S 1 = 1 ✓ · O 4 = 4 ✓ · charge: left 1(+2) + 1(−2) = 0, right 0 ✓
Sulfate stayed whole from the first line to the last. Its charge comes from the memorized list, and the charge check depends on it.
Dr. Karmach

Where this goes wrong

Splitting the solid into ions. Writing AgCl(s) as Ag⁺(aq) + Cl⁻(aq) lets every ion cancel, and the equation claims nothing happened. A solid formed. Only (aq) compounds separate; (s) stays intact.
Breaking up a polyatomic ion. Dissolved nitrate is NO₃⁻(aq), one whole unit with one charge. Cancel nitrate as nitrate, never as separate N and O.
Dropping the charges. Ag(aq) + Cl(aq) → AgCl(s) shows neutral atoms the water does not contain. Without charges, the charge check cannot be run.
Stopping at the complete ionic equation. If K⁺ and NO₃⁻ still stand on both sides, nothing has been cancelled. The net ionic equation keeps only the ions that build the solid.
Dr. Karmach

Practice 1

SrCl₂(aq) + Na₂CO₃(aq) → SrCO₃(s) + 2 NaCl(aq)
molecular — SrCO₃ is the precipitate

Strontium salts color fireworks red. Aqueous SrCl₂ and Na₂CO₃ are mixed, and SrCO₃ precipitates. Which is the correct net ionic equation?

  1. SrCl₂(aq) + Na₂CO₃(aq) → SrCO₃(s) + 2 NaCl(aq)
  2. Sr²⁺(aq) + 2 Cl⁻(aq) + 2 Na⁺(aq) + CO₃²⁻(aq) → SrCO₃(s) + 2 Na⁺(aq) + 2 Cl⁻(aq)
  3. Sr²⁺(aq) + CO₃²⁻(aq) → SrCO₃(s)
  4. Sr⁺(aq) + CO₃⁻(aq) → SrCO₃(s)
Dr. Karmach

Practice 1 — answer: C

SrCl₂(aq) + Na₂CO₃(aq) → SrCO₃(s) + 2 NaCl(aq)
the molecular equation, states from the solubility rules
Sr²⁺(aq) + CO₃²⁻(aq) → SrCO₃(s) — answer C
atoms: Sr 1 = 1 ✓ · C 1 = 1 ✓ · O 3 = 3 ✓ · charge: left 1(+2) + 1(−2) = 0, right 0 ✓

A is the molecular equation; nothing has been written as ions. B is the complete ionic equation: Na⁺ and Cl⁻ still stand on both sides, uncancelled. D halves both charges — strontium is a group 2 metal, Sr²⁺, and carbonate is CO₃²⁻, so its 1(+1) + 1(−1) = 0 only looks balanced.

An equation can pass the charge check with two wrong charges. Assign each ion's real charge first, then check.
Dr. Karmach

Worked example 3 — sodium chloride and potassium nitrate

Step 1 · Write the molecular equation with states

NaCl(aq) + KNO₃(aq) → NaNO₃(aq) + KCl(aq)
partners swapped — the solubility rules mark every compound (aq): no solid

The two solutions are mixed and stay clear: no solid, no gas, no color change. Write the complete ionic equation, then the net ionic equation.

Dr. Karmach

Worked example 3 — solution

NaCl(aq) + KNO₃(aq) → NaNO₃(aq) + KCl(aq)
molecular — every compound soluble, every state (aq)

Step 2 · Write each (aq) compound as its ions

Na⁺(aq) + Cl⁻(aq) + K⁺(aq) + NO₃⁻(aq) → Na⁺(aq) + NO₃⁻(aq) + K⁺(aq) + Cl⁻(aq)
complete ionic — no solid to keep intact
Dr. Karmach

Worked example 3 — solution

NaCl(aq) + KNO₃(aq) → NaNO₃(aq) + KCl(aq)
molecular — every compound soluble, every state (aq)
Step 2 · Write each (aq) compound as its ions
Na⁺(aq) + Cl⁻(aq) + K⁺(aq) + NO₃⁻(aq) → Na⁺(aq) + NO₃⁻(aq) + K⁺(aq) + Cl⁻(aq)
complete ionic — no solid to keep intact
Step 3 · Cancel the spectator ions

All four ions appear identical on both sides. Every ion is a spectator.

Na⁺(aq) + Cl⁻(aq) + K⁺(aq) + NO₃⁻(aq)Na⁺(aq) + NO₃⁻(aq) + K⁺(aq) + Cl⁻(aq)
4 − 4 = 0 ions remain — no net ionic equation
Dr. Karmach

Worked example 3 — solution

NaCl(aq) + KNO₃(aq) → NaNO₃(aq) + KCl(aq)
molecular — every compound soluble, every state (aq)
Step 2 · Write each (aq) compound as its ions
Na⁺(aq) + Cl⁻(aq) + K⁺(aq) + NO₃⁻(aq) → Na⁺(aq) + NO₃⁻(aq) + K⁺(aq) + Cl⁻(aq)
complete ionic — no solid to keep intact
Step 3 · Cancel the spectator ions
Na⁺(aq) + Cl⁻(aq) + K⁺(aq) + NO₃⁻(aq)Na⁺(aq) + NO₃⁻(aq) + K⁺(aq) + Cl⁻(aq)
4 − 4 = 0 ions remain — no net ionic equation
Mixing produced one solution holding the same four ions. When everything cancels, no reaction occurred — which is exactly what the clear beaker showed.
Dr. Karmach

Practice 2

Al(NO₃)₃(aq) + 3 NaOH(aq) → Al(OH)₃(s) + 3 NaNO₃(aq)
molecular — Al(OH)₃ is the precipitate

Water-treatment plants form Al(OH)₃ in the water; the fluffy solid traps fine dirt as it settles. Which is the correct net ionic equation?

  1. Al³⁺(aq) + 3 OH⁻(aq) → Al(OH)₃(s)
  2. Al³⁺(aq) + OH⁻(aq) → Al(OH)₃(s)
  3. Al³⁺(aq) + 3 NO₃⁻(aq) + 3 Na⁺(aq) + 3 OH⁻(aq) → Al(OH)₃(s) + 3 Na⁺(aq) + 3 NO₃⁻(aq)
  4. Al(NO₃)₃(aq) + 3 NaOH(aq) → Al(OH)₃(s) + 3 NaNO₃(aq)
Dr. Karmach

Practice 2 — answer: A

Al(NO₃)₃(aq) + 3 NaOH(aq) → Al(OH)₃(s) + 3 NaNO₃(aq)
the molecular equation, states from the solubility rules
Al³⁺(aq) + 3 OH⁻(aq) → Al(OH)₃(s) — answer A
atoms: Al 1 = 1 ✓ · O 3 = 3 ✓ · H 3 = 3 ✓ · charge: left 1(+3) + 3(−1) = 0, right 0 ✓

B dropped the coefficient: charge 1(+3) + 1(−1) = +2 against 0, and one OH cannot supply the three in Al(OH)₃. C is the complete ionic equation with Na⁺ and NO₃⁻ uncancelled. D is the molecular equation; no compound has been written as its ions.

Three 1− hydroxides balance one 3+ aluminum. The neutral solid fixes the 3 : 1 ratio, and the charge check confirms it.
Dr. Karmach

Check yourself

  1. K₂SO₄ dissolves in water. List the species actually present, with the charge and count of each.
  2. Cu²⁺(aq) + OH⁻(aq) → Cu(OH)₂(s) is offered as a net ionic equation. Run both checks; correct the equation.

Writing every (aq) compound as separated ions assumed each one separates completely. Some dissolved substances separate only partly, and sugar not at all: how completely a solute separates into ions classifies it as a strong, weak, or non-electrolyte.

Dr. Karmach

9 · Electrolytes & Dissociation

Classify a solute as a strong electrolyte, a weak electrolyte, or a nonelectrolyte from its compound type, and write its dissociation equation with the right ions, coefficients, and charge sum.

Dr. Karmach

Inside a sports drink

The label lists sodium, potassium, chloride. In the bottle, each one travels through the water as a separate charged particle. Nerve and muscle signals run on these moving charges.

Dr. Karmach

Conduction needs moving charges

A solution conducts only if charged particles can move through it. What a solute becomes in water sets how strongly its solution conducts: all ions, a few ions, or no ions at all.

Dr. Karmach

Three classes of solute

strong electrolyte — dissolves entirely as ions
soluble ionic compounds (NaOH, KOH included) · the strong acids: HCl · HBr · HI · HNO₃ · H₂SO₄ · HClO₄
weak electrolyte — a small fraction ionizes
weak acids and weak bases: HC₂H₃O₂ · NH₃ — most molecules stay whole
nonelectrolyte — dissolves as whole molecules
other molecular compounds: sugar · ethanol — no ions, no conduction

An electrolyte releases ions in water, and its solution conducts. Compound type assigns the class.

Dr. Karmach

Dissociation equations

NaCl(s) → Na⁺(aq) + Cl⁻(aq)
1 + 1 = 2 ions per formula unit · charge: (1+) + (1−) = 0
CaCl₂(s) → Ca²⁺(aq) + 2 Cl⁻(aq)
1 + 2 = 3 ions per formula unit · charge: (2+) + 2(1−) = 0

Water pulls an ionic solid apart into its separate ions: dissociation. Each ion keeps its identity and its charge. A subscript counts separate ions, so it becomes a coefficient.

Dr. Karmach

Polyatomic ions stay in one piece

Na₂SO₄(s) → 2 Na⁺(aq) + SO₄²⁻(aq)
2 + 1 = 3 ions · charge: 2(1+) + (2−) = 0

Dissociation separates cations from anions. It never breaks the bonds inside a polyatomic ion: sulfate enters the water whole, carrying its 2− charge.

Dr. Karmach

Weak electrolytes: partial ionization

HC₂H₃O₂(aq) ⇌ H⁺(aq) + C₂H₃O₂⁻(aq)
most molecules stay whole · each ionization: (1+) + (1−) = 0
NH₃(aq) + H₂O(l) ⇌ NH₄⁺(aq) + OH⁻(aq)
a weak base: only a few molecules react · charge: (1+) + (1−) = 0

A molecular acid or base ionizes: reaction with water makes new ions. A weak one barely reacts: a few molecules ionize, the rest stay whole. The double arrow marks an incomplete reaction.

Dr. Karmach

The method

  1. Classify the solute. Soluble ionic and strong acids: strong. Other acids and bases: weak. Other molecular: nonelectrolyte.
  2. Write what water makes. Separated ions, a few ions, or whole molecules.
  3. Check the charge sum. The ions must total zero.
Dr. Karmach

Worked example 1 — magnesium chloride

MgCl₂(s) dissolved in water
given: a soluble ionic compound · wanted: class + the dissociation equation

Road crews spread MgCl₂ as a de-icer, and it dissolves freely. Classify it and write the dissociation equation.

Dr. Karmach

Worked example 1 — solution

MgCl₂(s) dissolved in water
given: a soluble ionic compound · wanted: class + the dissociation equation

Step 1 · Classify the solute

A metal with a nonmetal: ionic. A soluble ionic compound is a strong electrolyte.

Dr. Karmach

Worked example 1 — solution

MgCl₂(s) dissolved in water
given: a soluble ionic compound · wanted: class + the dissociation equation
Step 1 · Classify the solute Step 2 · Write what water makes
MgCl₂(s) → Mg²⁺(aq) + 2 Cl⁻(aq)
subscript 2 → coefficient 2 · 1 + 2 = 3 ions per formula unit

The subscript counts two separate chloride ions. Each one leaves the lattice on its own.

Dr. Karmach

Worked example 1 — solution

MgCl₂(s) dissolved in water
given: a soluble ionic compound · wanted: class + the dissociation equation
Step 1 · Classify the solute Step 2 · Write what water makes
MgCl₂(s) → Mg²⁺(aq) + 2 Cl⁻(aq)
subscript 2 → coefficient 2 · 1 + 2 = 3 ions per formula unit
Step 3 · Check the charge sum
MgCl₂(s) → Mg²⁺(aq) + 2 Cl⁻(aq)
3 ions · charge: (2+) + 2(1−) = 0 ✓
Dr. Karmach

Worked example 1 — solution

MgCl₂(s) dissolved in water
given: a soluble ionic compound · wanted: class + the dissociation equation
Step 1 · Classify the solute Step 2 · Write what water makes
MgCl₂(s) → Mg²⁺(aq) + 2 Cl⁻(aq)
subscript 2 → coefficient 2 · 1 + 2 = 3 ions per formula unit
Step 3 · Check the charge sum
MgCl₂(s) → Mg²⁺(aq) + 2 Cl⁻(aq)
3 ions · charge: (2+) + 2(1−) = 0 ✓
The solid is neutral, so the ions it releases must cancel: one 2+ against two 1−. A nonzero sum marks a wrong formula or a wrong coefficient. ✓
Dr. Karmach

Worked example 2 — Na₂CO₃, NH₃, C₂H₅OH

Na₂CO₃ · NH₃ · C₂H₅OH
washing soda · household ammonia · ethanol — wanted: each class + what each solution contains

All three dissolve freely in water. Classify each and write what its solution contains.

Dr. Karmach

Worked example 2 — classifying

Na₂CO₃ · NH₃ · C₂H₅OH
washing soda · household ammonia · ethanol

Step 1 · Classify the solute

solute type class
Na₂CO₃ soluble ionic compound strong electrolyte
NH₃ molecular base, not an ionic hydroxide weak electrolyte
C₂H₅OH molecular, neither acid nor base nonelectrolyte
Dr. Karmach

Worked example 2 — classifying

Na₂CO₃ · NH₃ · C₂H₅OH
washing soda · household ammonia · ethanol

Step 1 · Classify the solute

solute type class
Na₂CO₃ soluble ionic compound strong electrolyte
NH₃ molecular base, not an ionic hydroxide weak electrolyte
C₂H₅OH molecular, neither acid nor base nonelectrolyte
All three bottles look identical. The compound type, not the appearance, separates them.
Dr. Karmach

Worked example 2 — what each solution contains

Na₂CO₃ · NH₃ · C₂H₅OH
classified: strong electrolyte · weak electrolyte · nonelectrolyte

Step 2 · Write what water makes Step 3 · Check the charge sum

Na₂CO₃(s) → 2 Na⁺(aq) + CO₃²⁻(aq)
2 + 1 = 3 ions · charge: 2(1+) + (2−) = 0 · carbonate stays one piece
Dr. Karmach

Worked example 2 — what each solution contains

Na₂CO₃ · NH₃ · C₂H₅OH
classified: strong electrolyte · weak electrolyte · nonelectrolyte

Step 2 · Write what water makes Step 3 · Check the charge sum

Na₂CO₃(s) → 2 Na⁺(aq) + CO₃²⁻(aq)
2 + 1 = 3 ions · charge: 2(1+) + (2−) = 0 · carbonate stays one piece
NH₃(aq) + H₂O(l) ⇌ NH₄⁺(aq) + OH⁻(aq)
a few ions · charge: (1+) + (1−) = 0 · most NH₃ molecules stay whole
Dr. Karmach

Worked example 2 — what each solution contains

Na₂CO₃ · NH₃ · C₂H₅OH
classified: strong electrolyte · weak electrolyte · nonelectrolyte

Step 2 · Write what water makes Step 3 · Check the charge sum

Na₂CO₃(s) → 2 Na⁺(aq) + CO₃²⁻(aq)
2 + 1 = 3 ions · charge: 2(1+) + (2−) = 0 · carbonate stays one piece
NH₃(aq) + H₂O(l) ⇌ NH₄⁺(aq) + OH⁻(aq)
a few ions · charge: (1+) + (1−) = 0 · most NH₃ molecules stay whole
C₂H₅OH(aq) — dissolves as whole molecules
0 ions · the OH is covalently bonded, not OH⁻
Dr. Karmach

Worked example 2 — what each solution contains

Na₂CO₃ · NH₃ · C₂H₅OH
classified: strong electrolyte · weak electrolyte · nonelectrolyte

Step 2 · Write what water makes Step 3 · Check the charge sum

Na₂CO₃(s) → 2 Na⁺(aq) + CO₃²⁻(aq)
2 + 1 = 3 ions · charge: 2(1+) + (2−) = 0 · carbonate stays one piece
NH₃(aq) + H₂O(l) ⇌ NH₄⁺(aq) + OH⁻(aq)
a few ions · charge: (1+) + (1−) = 0 · most NH₃ molecules stay whole
C₂H₅OH(aq) — dissolves as whole molecules
0 ions · the OH is covalently bonded, not OH⁻
Three clear solutions, three bulb readings: bright, dim, dark. ✓
Dr. Karmach

Your turn — magnesium nitrate

Mg(NO₃)₂(s) dissolved in water
given: a soluble ionic compound · nitrate: NO₃⁻
step work result
1 · classify the solute soluble ionic compound electrolyte
2 · write what water makes Mg(NO₃)₂(s) → Mg²⁺(aq) + ions per formula unit:
3 · check the charge sum (2+) + 2(1−) =

Complete the classification and the equation.

Dr. Karmach

Your turn — magnesium nitrate

Mg(NO₃)₂(s) dissolved in water
given: a soluble ionic compound · nitrate: NO₃⁻
step work result
1 · classify the solute soluble ionic compound electrolyte
2 · write what water makes Mg(NO₃)₂(s) → Mg²⁺(aq) + ions per formula unit:
3 · check the charge sum (2+) + 2(1−) =

Complete the classification and the equation.

Mg(NO₃)₂(s) → Mg²⁺(aq) + 2 NO₃⁻(aq)
strong electrolyte · 1 + 2 = 3 ions · charge: (2+) + 2(1−) = 0 · each nitrate leaves whole
Dr. Karmach

Where this goes wrong

Reading a subscript as a bonded pair. CaCl₂ never releases a Cl₂²⁻ unit. The subscript counts separate ions: Ca²⁺ + 2 Cl⁻ makes 1 + 2 = 3 ions, not 1 + 1 = 2.
Breaking a polyatomic ion into atoms. Na₂CO₃ gives 2 Na⁺ + CO₃²⁻ = 3 ions, never 2 + 1 + 3 = 6 pieces. Dissociation separates ions; it does not break the bonds inside one.
Calling sugar a weak electrolyte. Weak means a few ions form. Sugar forms none: its solution conducts no better than pure water. Nonelectrolyte.
Reading a molecular OH as hydroxide. Ethanol's OH is covalently bonded and stays put. Only ionic hydroxides such as NaOH release OH⁻.
Dr. Karmach

Practice 1

K₃PO₄ dissolved in water
given: a soluble ionic compound · phosphate: PO₄³⁻

Fertilizer-grade potassium phosphate dissolves freely in water. Which statement classifies it and describes what its solution contains?

  1. Weak electrolyte — a salt built around a polyatomic ion dissociates only partially
  2. Strong electrolyte — it dissociates completely into 3 K⁺ and PO₄³⁻, four ions per formula unit
  3. Strong electrolyte — it dissociates completely into K₃⁺ and PO₄³⁻, two ions per formula unit
  4. Nonelectrolyte — it dissolves as intact, neutral K₃PO₄ molecules
Dr. Karmach

Practice 1 — answer: B

K₃PO₄(s) → 3 K⁺(aq) + PO₄³⁻(aq) — answer B
3 + 1 = 4 ions · charge: 3(1+) + (3−) = 0

A: solubility decides, not the anion; a soluble salt dissociates completely, polyatomic ion or not. C: the subscript counts three separate K⁺ ions; no K₃⁺ unit exists, and 1 + 1 = 2 undercounts the ions. D: an ionic compound has no molecules; only separated ions enter the water.

Four ions from one formula unit, and the charges cancel: 3(1+) + (3−) = 0. ✓
Dr. Karmach

Worked example 3 — two acids

HNO₃ and HC₂H₃O₂, each dissolved in water
given: two molecular acids · wanted: each class + what each solution contains

Nitric acid and acetic acid both dissolve freely, in any proportion. A common first attempt: both are acids, so both ionize completely. Test it.

Dr. Karmach

Worked example 3 — solution

HNO₃ and HC₂H₃O₂, each dissolved in water

A common first attempt

both acids → all ions?
the strong-acid list: HCl · HBr · HI · HNO₃ · H₂SO₄ · HClO₄ — HC₂H₃O₂ is not on it ✗

Dissolving freely is not ionizing. Mixing spreads molecules through the water; only reaction with water makes ions.

Dr. Karmach

Worked example 3 — solution

HNO₃ and HC₂H₃O₂, each dissolved in water
A common first attempt
both acids → all ions?
the strong-acid list: HCl · HBr · HI · HNO₃ · H₂SO₄ · HClO₄ — HC₂H₃O₂ is not on it ✗
Step 1 · Classify the solute

HNO₃ is on the list: a strong electrolyte. HC₂H₃O₂ is not, and an acid off the list is weak.

Dr. Karmach

Worked example 3 — solution

HNO₃ and HC₂H₃O₂, each dissolved in water
A common first attempt
both acids → all ions?
the strong-acid list: HCl · HBr · HI · HNO₃ · H₂SO₄ · HClO₄ — HC₂H₃O₂ is not on it ✗
Step 1 · Classify the solute Step 2 · Write what water makes Step 3 · Check the charge sum
HNO₃(aq) → H⁺(aq) + NO₃⁻(aq)
every molecule ionizes · 1 + 1 = 2 ions · charge: (1+) + (1−) = 0
HC₂H₃O₂(aq) ⇌ H⁺(aq) + C₂H₃O₂⁻(aq)
a few molecules ionize, the rest stay whole · charge: (1+) + (1−) = 0
Dr. Karmach

Worked example 3 — solution

HNO₃ and HC₂H₃O₂, each dissolved in water
A common first attempt
both acids → all ions?
the strong-acid list: HCl · HBr · HI · HNO₃ · H₂SO₄ · HClO₄ — HC₂H₃O₂ is not on it ✗
Step 1 · Classify the solute Step 2 · Write what water makes Step 3 · Check the charge sum
HNO₃(aq) → H⁺(aq) + NO₃⁻(aq)
every molecule ionizes · 1 + 1 = 2 ions · charge: (1+) + (1−) = 0
HC₂H₃O₂(aq) ⇌ H⁺(aq) + C₂H₃O₂⁻(aq)
a few molecules ionize, the rest stay whole · charge: (1+) + (1−) = 0
Both conduct, not equally: HNO₃ all ions, HC₂H₃O₂ mostly whole molecules — a dim bulb. ✓
Dr. Karmach

Take-home: dissolving is not ionizing

HNO₃ — on the strong-acid list
dissolves freely and ionizes completely: all ions in solution
HC₂H₃O₂ — not on the list
dissolves just as freely, barely ionizes: mostly whole molecules

Solubility measures how much dissolves. Electrolyte strength measures what the dissolved substance becomes. An acid is a strong electrolyte only if it is on the memorized list; every other acid is weak.

Dr. Karmach

Practice 2

HF dissolved in water
given: a molecular acid · wanted: class + what the solution contains

Glass etchers work with HF dissolved in water. Which statement classifies it and describes what its solution contains?

  1. Strong electrolyte — HF is an acid, and acids ionize completely in water
  2. Nonelectrolyte — HF is molecular, so it dissolves without forming any ions
  3. Weak electrolyte — most HF molecules stay whole; a small fraction ionizes to H⁺ and F⁻
  4. Weak electrolyte — each HF molecule that ionizes produces three ions: one H⁺, one H₃O⁺, and one F⁻
Dr. Karmach

Practice 2 — answer: C

HF(aq) ⇌ H⁺(aq) + F⁻(aq) — answer C
a few molecules ionize · 1 + 1 = 2 ions each · charge: (1+) + (1−) = 0

A: the list is HCl, HBr, HI, HNO₃, H₂SO₄, HClO₄; HF is not on it, and an acid off the list is weak. B: a small fraction does ionize, so the solution conducts weakly; a nonelectrolyte would not conduct at all. D: H⁺ and H₃O⁺ are two names for the same ion, so 1 + 1 + 1 = 3 counts it twice; each ionized HF gives 1 + 1 = 2 ions.

Weak means few ions, never zero. The few that form still cancel: (1+) + (1−) = 0. ✓
Dr. Karmach

Check yourself

  1. K₂S dissolves freely in water. Name its class, write the dissociation equation, and check the ion tally and the charge sum.
  2. A solution conducts, but only faintly. Which class is the solute, and what does the solution mostly contain?

Every dissolved ion in these equations carries a definite charge. The oxidation number extends that bookkeeping to every atom in any formula, and it tracks the electron transfers behind redox reactions.

Dr. Karmach

10 · Oxidation Numbers

Assign oxidation numbers by the priority rules, and find any element the rules skip by setting the sum equal to the species' charge.

Dr. Karmach

Rust, bleach, and batteries

A nail rusts. Bleach lifts a stain. A battery lights a bulb. In each change, atoms give electrons to other atoms. A number on each atom keeps count.

Dr. Karmach

The oxidation number

H₂O → H: +1 · O: −2
2(+1) + 1(−2) = 0 ✓ — the numbers sum to the compound's charge

An atom's oxidation number is the charge it would carry if the shared electrons were assigned by rule. The rules form a priority list. One check governs every assignment: the numbers sum to the species' charge.

Dr. Karmach

The rules, in priority order

Work down the list. The first rule that applies to an element wins. Most elements have no rule of their own; their numbers come from the sum.

Dr. Karmach

Oxidation number and ionic charge

Ca²⁺ → oxidation number +2
a monatomic ion — the number is the ion's real charge
CO₂ → C: +4 · O: −2 each
4 + 2(−2) = 0 ✓ — no C⁴⁺ ion here; the atoms share electrons

A monatomic ion's oxidation number is its charge. In a molecule, no atom holds a full charge; the number records assigned electrons. It is written sign-first: +4, not 4+.

Dr. Karmach

What the sum must equal

H₂O — a neutral compound
H: +1, +1 · O: −2 — 2(+1) + 1(−2) = 0, the compound's charge
OH⁻ — a polyatomic ion
O: −2 · H: +1 — 1(−2) + 1(+1) = −1, the ion's charge

A neutral compound's numbers sum to zero. A polyatomic ion's numbers sum to the charge written on the ion — never to zero.

Dr. Karmach

The method

  1. Assign the known numbers. The first rule that applies wins.
  2. Multiply by the subscripts.
  3. Set the sum equal to the charge. Neutral compound: 0. Polyatomic ion: its charge.
  4. Solve for the unknown.
Dr. Karmach

Worked example 1 — SO₂

SO₂
given: a neutral compound · wanted: every oxidation number

Sulfur dioxide forms when coal burns. Assign an oxidation number to each element.

Dr. Karmach

Worked example 1 — solution

SO₂
given: a neutral compound · wanted: every oxidation number

Step 1 · Assign the known numbers

Oxygen's rule gives −2. Sulfur has no rule of its own: call it x.

Dr. Karmach

Worked example 1 — solution

SO₂
given: a neutral compound · wanted: every oxidation number
Step 1 · Assign the known numbers Step 2 · Multiply by the subscripts Step 3 · Set the sum equal to the charge

Two O atoms contribute 2(−2) = −4. The compound is neutral, so the sum is 0.

x + 2(−2) = 0
S: x · O: −2 each, 2 atoms → −4 · neutral → sum 0
Dr. Karmach

Worked example 1 — solution

SO₂
given: a neutral compound · wanted: every oxidation number
Step 1 · Assign the known numbers Step 2 · Multiply by the subscripts Step 3 · Set the sum equal to the charge
x + 2(−2) = 0
S: x · O: −2 each, 2 atoms → −4 · neutral → sum 0
Step 4 · Solve for the unknown
x = 0 + 4 = +4
S: +4 · O: −2, −2 — check: +4 + 2(−2) = 0 ✓
Dr. Karmach

Worked example 1 — solution

SO₂
given: a neutral compound · wanted: every oxidation number
Step 1 · Assign the known numbers Step 2 · Multiply by the subscripts Step 3 · Set the sum equal to the charge
x + 2(−2) = 0
S: x · O: −2 each, 2 atoms → −4 · neutral → sum 0
Step 4 · Solve for the unknown
x = 0 + 4 = +4
S: +4 · O: −2, −2 — check: +4 + 2(−2) = 0 ✓
The numbers sum to 0, a neutral compound's charge. No S⁴⁺ ion exists in SO₂; +4 records assigned electrons, not a real charge.
Dr. Karmach

Worked example 2 — KMnO₄

KMnO₄
given: a neutral compound · wanted: the oxidation number of Mn

Potassium permanganate is a deep purple disinfectant. Two of its three elements have rules. Find the oxidation number of Mn.

Dr. Karmach

Worked example 2 — solution

KMnO₄
given: a neutral compound · wanted: the oxidation number of Mn

Step 1 · Assign the known numbers

Potassium is Group 1: +1. Oxygen's rule gives −2. Manganese has no rule of its own: call it x.

Dr. Karmach

Worked example 2 — solution

KMnO₄
given: a neutral compound · wanted: the oxidation number of Mn
Step 1 · Assign the known numbers Step 2 · Multiply by the subscripts Step 3 · Set the sum equal to the charge

Four O atoms contribute 4(−2) = −8. The compound is neutral, so the sum is 0.

(+1) + x + 4(−2) = 0
K: +1 · Mn: x · O: −2 each, 4 atoms → −8 · neutral → sum 0
Dr. Karmach

Worked example 2 — solution

KMnO₄
given: a neutral compound · wanted: the oxidation number of Mn
Step 1 · Assign the known numbers Step 2 · Multiply by the subscripts Step 3 · Set the sum equal to the charge
(+1) + x + 4(−2) = 0
K: +1 · Mn: x · O: −2 each, 4 atoms → −8 · neutral → sum 0
Step 4 · Solve for the unknown
x = 0 − 1 + 8 = +7
K: +1 · Mn: +7 · O: −2 ×4 — check: +1 + 7 + 4(−2) = 0 ✓
Dr. Karmach

Worked example 2 — solution

KMnO₄
given: a neutral compound · wanted: the oxidation number of Mn
Step 1 · Assign the known numbers Step 2 · Multiply by the subscripts Step 3 · Set the sum equal to the charge
(+1) + x + 4(−2) = 0
K: +1 · Mn: x · O: −2 each, 4 atoms → −8 · neutral → sum 0
Step 4 · Solve for the unknown
x = 0 − 1 + 8 = +7
K: +1 · Mn: +7 · O: −2 ×4 — check: +1 + 7 + 4(−2) = 0 ✓
+1 + 7 − 8 = 0 ✓. An element without a rule of its own gets its number from the sum.
Dr. Karmach

Your turn — H₂SO₄

H₂SO₄
given: a neutral compound · wanted: the oxidation number of S
step work
1 · assign the known numbers H: +1 · O: −2 · S: x
2 · multiply by the subscripts 2(+1) = +2 · 4(−2) =
3 · set the sum equal to the charge +2 + x + (−8) =
4 · solve for the unknown x =

Complete the table.

Dr. Karmach

Your turn — H₂SO₄

H₂SO₄
given: a neutral compound · wanted: the oxidation number of S
step work
1 · assign the known numbers H: +1 · O: −2 · S: x
2 · multiply by the subscripts 2(+1) = +2 · 4(−2) =
3 · set the sum equal to the charge +2 + x + (−8) =
4 · solve for the unknown x =

Complete the table.

2(+1) + x + 4(−2) = 0 → x = +6
H: +1, +1 · S: +6 · O: −2 ×4 — check: +2 + 6 − 8 = 0 ✓
Dr. Karmach

Where this goes wrong

Counting the −2 once for the whole formula. In CO₃²⁻, x + (−2) = −2 gives x = 0. The −2 belongs to each O atom: three of them contribute 3(−2) = −6, and x + (−6) = −2 gives x = +4.
Putting the unknown on the negative side. In ClO₃⁻, writing Cl as −5 sums to −5 − 6 = −11, not −1. Oxygen already holds the negative numbers; Cl balances them from the positive side: −1 + 6 = +5.
Giving H +1 next to a metal. In NaH, that reads +1 + 1 = +2, not 0. Sodium's rule sits higher on the list, so Na is +1 and H takes −1: +1 − 1 = 0 ✓.
Giving O −2 in a peroxide. In H₂O₂, that reads 2(+1) + 2(−2) = −2, not 0. Peroxide oxygen is −1: 2(+1) + 2(−1) = 0 ✓.
Dr. Karmach

Worked example 3 — SO₄²⁻

Step 1 · Assign the known numbers

SO₄²⁻
O: −2 each (rule) · S: x · wanted: the oxidation number of S

The sulfate ion appears in fertilizer and hard water. A common first attempt sets the sum to zero. Test it.

Dr. Karmach

Worked example 3 — testing the first attempt

SO₄²⁻
O: −2 each (rule) · S: x · wanted: the oxidation number of S

A common first attempt

x + 4(−2) = 0 → x = +8
sum: +8 − 8 = 0 ✗ — but SO₄²⁻ is not neutral
Dr. Karmach

Worked example 3 — testing the first attempt

SO₄²⁻
O: −2 each (rule) · S: x · wanted: the oxidation number of S

A common first attempt

x + 4(−2) = 0 → x = +8
sum: +8 − 8 = 0 ✗ — but SO₄²⁻ is not neutral
A sum of zero describes a neutral species. This ion carries 2−.
The check must land on the charge written on the species: −2, not 0.
Dr. Karmach

Worked example 3 — solution

SO₄²⁻
O: −2 each (rule) · S: x · wanted: the oxidation number of S

Step 2 · Multiply by the subscripts Step 3 · Set the sum equal to the charge

Four O atoms contribute 4(−2) = −8. The species is an ion, so the sum is its charge: −2.

x + 4(−2) = −2
S: x · O: −2 each, 4 atoms → −8 · ion → sum −2, not 0
Dr. Karmach

Worked example 3 — solution

SO₄²⁻
O: −2 each (rule) · S: x · wanted: the oxidation number of S
Step 2 · Multiply by the subscripts Step 3 · Set the sum equal to the charge
x + 4(−2) = −2
S: x · O: −2 each, 4 atoms → −8 · ion → sum −2, not 0
Step 4 · Solve for the unknown
x = −2 + 8 = +6
S: +6 · O: −2 ×4 — check: +6 − 8 = −2 ✓, the ion's charge
Dr. Karmach

Worked example 3 — solution

SO₄²⁻
O: −2 each (rule) · S: x · wanted: the oxidation number of S
Step 2 · Multiply by the subscripts Step 3 · Set the sum equal to the charge
x + 4(−2) = −2
S: x · O: −2 each, 4 atoms → −8 · ion → sum −2, not 0
Step 4 · Solve for the unknown
x = −2 + 8 = +6
S: +6 · O: −2 ×4 — check: +6 − 8 = −2 ✓, the ion's charge
+6 − 8 = −2 ✓. The first attempt's +8 fails the same check: +8 − 8 = 0 ≠ −2.
Dr. Karmach

Take-home: an ion's numbers sum to the ion's charge

Zero is reserved for neutral species. H₂SO₄ sums to 0; SO₄²⁻ sums to −2. Both give S +6 — the target changes, not the rules.

Dr. Karmach

Practice 1

CrO₄²⁻
the chromate ion · O: −2 each (rule) · Cr: x

Chromate gives some paint pigments their yellow color. What is the oxidation number of Cr in CrO₄²⁻?

  1. +8
  2. +6
  3. 0
  4. −6
Dr. Karmach

Practice 1 — answer: B

x + 4(−2) = −2 → x = −2 + 8 = +6 — answer B
Cr: +6 · O: −2 ×4 — check: +6 − 8 = −2 ✓, the ion's charge

A set the sum to zero: x + 4(−2) = 0 → +8, a neutral species' answer. C counted the −2 once for the whole ion: x + (−2) = −2 → 0; four O atoms contribute −8. D put the unknown on the negative side: −6 − 8 = −14, not −2.

+6 − 8 = −2 — the sum lands exactly on the charge written on the ion.
Dr. Karmach

Practice 2

PO₄³⁻
the phosphate ion · O: −2 each (rule) · P: x

Fertilizer supplies phosphorus as the phosphate ion. What is the oxidation number of P in PO₄³⁻?

  1. +8
  2. −5
  3. +5
  4. −1
Dr. Karmach

Practice 2 — answer: C

x + 4(−2) = −3 → x = −3 + 8 = +5 — answer C
P: +5 · O: −2 ×4 — check: +5 − 8 = −3 ✓, the ion's charge

A set the sum to zero: x + 4(−2) = 0 → +8. B put the unknown on the negative side: −5 − 8 = −13, not −3. D counted the −2 once for the whole ion: x + (−2) = −3 → −1; four O atoms contribute −8.

+5 − 8 = −3 ✓ — a 3− ion's numbers must sum to −3.
Dr. Karmach

Check yourself

  1. Assign every oxidation number in Na₂CrO₄. Which element's number comes from the sum?
  2. In NO₃⁻, what must the numbers sum to, and what number does N carry?

When a reaction runs, these numbers can change. An element whose number rises has lost electrons; one whose number falls has gained them. Those changes mark oxidation and reduction, and the reactants that cause them are the oxidizing and reducing agents.

Dr. Karmach

11 · Oxidizing & Reducing Agents

Decide from oxidation-number changes whether a reaction is redox, tell what is oxidized and what is reduced, and name the oxidizing and reducing agents.

Dr. Karmach

Silver grows on copper

A copper wire stands overnight in dissolved silver. Solid silver collects on the wire; the liquid turns blue with dissolved copper. The two metals have traded places.

Dr. Karmach

Electrons never vanish

Some reactions move electrons from one substance to another. Every electron one atom loses, another atom gains. Oxidation numbers make the transfer visible: they change only where electrons leave or arrive.

Dr. Karmach

Oxidation and reduction

oxidation — the oxidation number increases: electrons lost
Zn + Cu²⁺ → Zn²⁺ + Cu · Zn: 0 → +2 — zinc is oxidized
reduction — the oxidation number decreases: electrons gained
Zn + Cu²⁺ → Zn²⁺ + Cu · Cu: +2 → 0 — copper is reduced

Assign oxidation numbers to both sides and compare. OIL RIG: Oxidation Is Loss, Reduction Is Gain — a loss always pairs with a gain.

Dr. Karmach

Naming the agents

oxidizing agent — the reactant containing the atom that is reduced
it takes electrons: it oxidizes its partner
reducing agent — the reactant containing the atom that is oxidized
it gives electrons: it reduces its partner

Each agent is named for what it does to its partner, not for what happens to itself. Both agents are reactants: name the whole substance, not just the atom.

Dr. Karmach

The method

  1. Assign oxidation numbers to every atom, both sides.
  2. Find the changes: an increase is oxidation, a decrease is reduction.
  3. Name the agents: the reduced atom's reactant is the oxidizing agent; the oxidized atom's is the reducing agent.
Dr. Karmach

Worked example 1 — zinc in copper(II) sulfate

Step 1 · Assign oxidation numbers

Zn + CuSO₄ → ZnSO₄ + Cu
Zn: 0 → +2 · Cu: +2 → 0 · S: +6 → +6 · O: −2 → −2

A zinc strip in blue copper(II) sulfate solution darkens with copper, a single-displacement reaction. Elements by themselves count 0; O is −2; sulfate's sum, x + 4(−2) = −2, gives S +6; Cu balances its neutral formula at +2.

Which element is oxidized, and which is reduced?

Dr. Karmach

Worked example 1 — solution

Zn + CuSO₄ → ZnSO₄ + Cu
Zn: 0 → +2 · Cu: +2 → 0 · S: +6 → +6 · O: −2 → −2

Step 2 · Find the changes

Zn increases, 0 → +2: zinc is oxidized. It lost 2 electrons. Cu decreases, +2 → 0: copper is reduced. It gained 2 electrons.

Dr. Karmach

Worked example 1 — solution

Zn + CuSO₄ → ZnSO₄ + Cu
Zn: 0 → +2 · Cu: +2 → 0 · S: +6 → +6 · O: −2 → −2
Step 2 · Find the changes The unchanged atoms

S stays +6 and O stays −2. The sulfate group moves as one piece; no atom in it loses or gains anything. The transfer runs between Zn and Cu only.

Dr. Karmach

Worked example 1 — solution

Zn + CuSO₄ → ZnSO₄ + Cu
Zn: 0 → +2 · Cu: +2 → 0 · S: +6 → +6 · O: −2 → −2
Step 2 · Find the changes The unchanged atoms
Electrons lost = electrons gained: Zn lost 2, Cu gained 2. A reaction cannot lose electrons without something gaining them.
Dr. Karmach

Worked example 2 — copper in silver nitrate

Step 1 · Assign oxidation numbers

Cu + 2 AgNO₃ → Cu(NO₃)₂ + 2 Ag
Cu: 0 → +2 · Ag: +1 → 0 · N: +5 → +5 · O: −2 → −2

A copper wire in silver nitrate solution grows silver crystals while the liquid turns blue. Elements count 0; O is −2; nitrate's sum, x + 3(−2) = −1, gives N +5; Ag and Cu balance their formulas at +1 and +2.

Name both agents. A common first answer: copper is oxidized, so copper is the oxidizing agent. Test it against the definitions.

Dr. Karmach

Worked example 2 — solution

Cu + 2 AgNO₃ → Cu(NO₃)₂ + 2 Ag
Cu: 0 → +2 · Ag: +1 → 0 · N: +5 → +5 · O: −2 → −2

Step 2 · Find the changes

Cu increases, 0 → +2: copper is oxidized, losing 2 electrons. Ag decreases, +1 → 0: silver is reduced, each atom gaining 1 electron. N and O do not change.

Dr. Karmach

Worked example 2 — solution

Cu + 2 AgNO₃ → Cu(NO₃)₂ + 2 Ag
Cu: 0 → +2 · Ag: +1 → 0 · N: +5 → +5 · O: −2 → −2
Step 2 · Find the changes A common first answer

Copper is oxidized. That does not make it the oxidizing agent: the name describes what a reactant does to its partner. Copper gives its electrons away and oxidizes nothing. The silver in AgNO₃ takes them, so AgNO₃ does the oxidizing.

Dr. Karmach

Worked example 2 — solution

Cu + 2 AgNO₃ → Cu(NO₃)₂ + 2 Ag
Cu: 0 → +2 · Ag: +1 → 0 · N: +5 → +5 · O: −2 → −2
Step 2 · Find the changes A common first answer Step 3 · Name the agents
agent substance evidence
oxidizing agent AgNO₃ contains Ag, reduced +1 → 0
reducing agent Cu oxidized 0 → +2
Dr. Karmach

Worked example 2 — solution

Cu + 2 AgNO₃ → Cu(NO₃)₂ + 2 Ag
Cu: 0 → +2 · Ag: +1 → 0 · N: +5 → +5 · O: −2 → −2
Step 2 · Find the changes A common first answer Step 3 · Name the agents
agent substance evidence
oxidizing agent AgNO₃ contains Ag, reduced +1 → 0
reducing agent Cu oxidized 0 → +2
Electrons lost = gained: Cu lost 2; 2 Ag × 1 e⁻ = 2 gained. The oxidized copper is the reducing agent.
Dr. Karmach

Take-home: the oxidized substance is the reducing agent

An agent's name tells what it does to its partner. The oxidized substance gives electrons: the reducing agent. The reduced substance takes them: the oxidizing agent.

Dr. Karmach

Your turn — magnesium in hydrochloric acid

Mg + 2 HCl → MgCl₂ + H₂
Mg: 0 → · H: +1 → · Cl: −1 → −1
question answer
oxidized / reduced
oxidizing agent
reducing agent

Complete the two changes, then name both agents.

Dr. Karmach

Your turn — magnesium in hydrochloric acid

Mg + 2 HCl → MgCl₂ + H₂
Mg: 0 → · H: +1 → · Cl: −1 → −1
question answer
oxidized / reduced
oxidizing agent
reducing agent

Complete the two changes, then name both agents.

Mg + 2 HCl → MgCl₂ + H₂
Mg: 0 → +2 — oxidized · H: +1 → 0 — reduced · Cl: −1 → −1 unchanged

HCl contains the reduced H: the oxidizing agent. Mg is oxidized: the reducing agent. Electrons: Mg lost 2; 2 H × 1 e⁻ = 2 gained. ✓

Dr. Karmach

Where this goes wrong

Swapping the two agents. In Zn + CuSO₄ → ZnSO₄ + Cu, calling Zn the oxidizing agent and CuSO₄ the reducing agent reverses both names. CuSO₄ takes zinc's electrons, and the reactant that takes electrons does the oxidizing.
Calling the oxidized substance the oxidizing agent. Being oxidized means giving electrons to the partner, and giving electrons is what reduces the partner. The oxidized substance is always the reducing agent.
Picking a spectator as the agent. In Cu + 2 AgNO₃ → Cu(NO₃)₂ + 2 Ag, nitrate moves from silver to copper, yet N stays +5 and O stays −2. Changing partners moves no electrons. Agents contain atoms whose numbers change.
Dr. Karmach

Practice 1

Ni + CuCl₂ → NiCl₂ + Cu

A nickel bar sits in green copper(II) chloride solution and slowly plates with copper. Which species is the oxidizing agent?

  1. Ni, because it is the species that gets oxidized.
  2. CuCl₂, because it contains Cu, which is reduced from +2 to 0.
  3. The chloride ion, Cl⁻: it changes partners during the reaction, so it drives the electron transfer.
  4. Ni is the oxidizing agent, and CuCl₂ is the reducing agent.
Dr. Karmach

Practice 1 — answer: B

Ni + CuCl₂ → NiCl₂ + Cu
Ni: 0 → +2 — oxidized · Cu: +2 → 0 — reduced · Cl: −1 → −1 unchanged
Cu: +2 → 0 · reduced · its reactant is CuCl₂ = the oxidizing agent — answer B

A named the oxidized species: losing electrons to the partner is exactly what makes Ni the reducing agent. C followed the partner-swapping: Cl is −1 on both sides, a change of (−1) − (−1) = 0, so chloride transferred nothing. D swapped both names: CuCl₂ takes nickel's electrons, and the taker does the oxidizing.

Electrons lost = gained: Ni lost 2, Cu gained 2. ✓
Dr. Karmach

Worked example 3 — testing whether a reaction is redox

Pb(NO₃)₂ + 2 KI → PbI₂ + 2 KNO₃

Two colorless solutions mix and a bright yellow solid, PbI₂, appears. Every formula changes partners.

Assign oxidation numbers to both sides: is any element oxidized or reduced?

Dr. Karmach

Worked example 3 — solution

Step 1 · Assign oxidation numbers

K, a group 1A metal, is +1; the iodide ion is −1; O is −2; nitrate's sum, x + 3(−2) = −1, gives N +5; Pb balances each formula at +2.

Pb(NO₃)₂ + 2 KI → PbI₂ + 2 KNO₃
Pb: +2 → +2 · N: +5 → +5 · O: −2 → −2 · K: +1 → +1 · I: −1 → −1
Dr. Karmach

Worked example 3 — solution

Step 1 · Assign oxidation numbers

Pb(NO₃)₂ + 2 KI → PbI₂ + 2 KNO₃
Pb: +2 → +2 · N: +5 → +5 · O: −2 → −2 · K: +1 → +1 · I: −1 → −1
Step 2 · Find the changes

Every number is the same on both sides. Nothing is oxidized and nothing is reduced: no electrons moved. This reaction is not redox, and it has no oxidizing or reducing agent.

Dr. Karmach

Worked example 3 — solution

Step 1 · Assign oxidation numbers

Pb(NO₃)₂ + 2 KI → PbI₂ + 2 KNO₃
Pb: +2 → +2 · N: +5 → +5 · O: −2 → −2 · K: +1 → +1 · I: −1 → −1
Step 2 · Find the changes
Electrons lost = gained: 0 = 0. A yellow precipitate is a real reaction, but ions that keep their numbers have only changed partners.
Dr. Karmach

Practice 2 — halogens

Cl₂ + 2 KBr → 2 KCl + Br₂

Chlorine gas bubbled through potassium bromide solution turns it orange with bromine. Which species is the oxidizing agent?

  1. KBr, because it is the species that gets oxidized.
  2. The potassium ion, K⁺: it changes partners during the reaction, so it drives the electron transfer.
  3. Cl₂, because it contains Cl, which is reduced from 0 to −1.
  4. KBr is the oxidizing agent, and Cl₂ is the reducing agent.
Dr. Karmach

Practice 2 — answer: C

Cl₂ + 2 KBr → 2 KCl + Br₂
Cl: 0 → −1 — reduced · Br: −1 → 0 — oxidized · K: +1 → +1 unchanged
Cl: 0 → −1 · reduced · its reactant is Cl₂ = the oxidizing agent — answer C

A named the oxidized species: KBr gives its electrons away, which makes it the reducing agent. B followed the partner-swapping: K is +1 in KBr and +1 in KCl, a change of 1 − 1 = 0. D swapped both names: Cl₂ takes bromide's electrons, and the taker does the oxidizing. An oxidizing agent need not contain a metal.

Electrons lost = gained: 2 Br × 1 e⁻ = 2 lost; 2 Cl × 1 e⁻ = 2 gained. ✓
Dr. Karmach

Check yourself

  1. In Fe + CuSO₄ → FeSO₄ + Cu, iron goes 0 → +2. Which reactant is the reducing agent, and which element took iron's electrons?
  2. In 2 Al + 6 HCl → 2 AlCl₃ + 3 H₂, aluminum goes 0 → +3. How many electrons move in total, and where do they end up?

A balanced equation promises a maximum amount of product. The amount actually collected, compared with that maximum, is the percent yield.

Dr. Karmach

12 · Percent Yield

Compare the mass a reaction actually delivers to the maximum stoichiometry allows, and report it as a percent yield.

Dr. Karmach

Three cookies short

A cookie recipe promises two dozen. The tray comes out with 21: batter stuck to the bowl, one burned. Chemical reactions come up short the same way.

Dr. Karmach

Theoretical yield: the maximum stoichiometry allows

2 Mg + O₂ → 2 MgO
given: 10.0 g Mg · the chain g Mg → mol Mg → mol MgO → g MgO allows at most 16.6 g

Mass-to-mass stoichiometry computes the most product the given amounts can form: the theoretical yield. A real experiment collects less. Percent yield reports how much of that maximum was actually delivered.

Dr. Karmach

Actual yield is measured, never computed

2 Mg + O₂ → 2 MgO
theoretical: 16.6 g MgO — computed · actual: 14.1 g MgO — weighed

The actual yield is the mass of product collected, read off the balance after the experiment. No calculation predicts it. Every percent-yield problem states it.

Dr. Karmach

Where the missing mass goes

Side reactions consume reactant without making the product. Some reactant never reacts. Some product stays behind in transfer — on the filter, in the crucible. Every loss lowers the actual yield.

Dr. Karmach

Percent yield

percent yield = actual yield ÷ theoretical yield × 100
actual — weighed · theoretical — computed · same substance, same unit

Both masses refer to the product. The fraction compares the collected mass to the maximum; × 100 states it as a percent. A real preparation lands below 100%.

Dr. Karmach

The method

  1. Compute the theoretical yield: the maximum product mass from the given amounts. Two reactant amounts given: work from the limiting reactant.
  2. Take the actual yield from the problem — measured, never computed.
  3. Divide: actual ÷ theoretical × 100.
Dr. Karmach

Worked example 1 — heating limestone

CaCO₃ → CaO + CO₂
given: 50.0 g CaCO₃ · actual: 18.5 g CO₂ collected · wanted: percent yield

A kiln charge of 50.0 g CaCO₃ is heated until no more gas comes off. The CO₂ collected weighs 18.5 g. What is the percent yield? (CaCO₃ 100.09 g/mol · CO₂ 44.01 g/mol)

A common first attempt: 18.5 ÷ 50.0 × 100 = 37.0%. Test it.

Dr. Karmach

Worked example 1 — solution

CaCO₃ → CaO + CO₂
given: 50.0 g CaCO₃ · actual: 18.5 g CO₂

Three conversion factors build the theoretical yield.

Step 1 · Compute the theoretical yield

50.0 g CaCO₃ × 1 mol CaCO₃100.09 g CaCO₃ × 1 mol CO₂1 mol CaCO₃ × 44.01 g CO₂1 mol CO₂ = 22.0 g CO₂
Dr. Karmach

Worked example 1 — solution

CaCO₃ → CaO + CO₂
given: 50.0 g CaCO₃ · actual: 18.5 g CO₂
Step 1 · Compute the theoretical yield
50.0 g CaCO₃ × 1 mol CaCO₃100.09 g CaCO₃ × 1 mol CO₂1 mol CaCO₃ × 44.01 g CO₂1 mol CO₂ = 22.0 g CO₂
Step 2 · Take the actual yield from the problem

The balance reads 18.5 g. The first attempt divided by 50.0 g of CaCO₃ — a different substance. The 100% mark is 22.0 g: the most CO₂ this charge can form.

Dr. Karmach

Worked example 1 — solution

CaCO₃ → CaO + CO₂
given: 50.0 g CaCO₃ · actual: 18.5 g CO₂
Step 1 · Compute the theoretical yield
50.0 g CaCO₃ × 1 mol CaCO₃100.09 g CaCO₃ × 1 mol CO₂1 mol CaCO₃ × 44.01 g CO₂1 mol CO₂ = 22.0 g CO₂
Step 2 · Take the actual yield from the problem Step 3 · Divide: actual ÷ theoretical × 100
18.5 g CO₂22.0 g CO₂ × 100 = 84.1%
Dr. Karmach

Worked example 1 — solution

CaCO₃ → CaO + CO₂
given: 50.0 g CaCO₃ · actual: 18.5 g CO₂
Step 1 · Compute the theoretical yield
50.0 g CaCO₃ × 1 mol CaCO₃100.09 g CaCO₃ × 1 mol CO₂1 mol CaCO₃ × 44.01 g CO₂1 mol CO₂ = 22.0 g CO₂
Step 2 · Take the actual yield from the problem Step 3 · Divide: actual ÷ theoretical × 100
18.5 g CO₂22.0 g CO₂ × 100 = 84.1%
Below 100% ✓. Of every 100 g of CO₂ the equation allows, the kiln delivered 84. The 37.0% first attempt compared product to reactant, not product to product.
Dr. Karmach

Take-home: percent yield compares product to product

CaCO₃ → CaO + CO₂
given: 50.0 g CaCO₃ · actual: 18.5 g CO₂ · theoretical: 22.0 g CO₂

Do: divide the product collected by the product possible.

18.5 g CO₂ ÷ 22.0 g CO₂ × 100 = 84.1%
actual product over theoretical product ✓

Do not: divide by the starting mass.

18.5 g CO₂ ÷ 50.0 g CaCO₃ × 100 = 37.0%
product over reactant — different substances, not a yield ✗
Dr. Karmach

Worked example 2 — two reactant amounts

Pb(NO₃)₂ + 2 KI → PbI₂ + 2 KNO₃
given: 15.0 g Pb(NO₃)₂ and 12.0 g KI · actual: 14.2 g PbI₂ · wanted: percent yield

Two clear solutions are mixed and bright yellow PbI₂ precipitates. The dried solid weighs 14.2 g. What is the percent yield? (Pb(NO₃)₂ 331.2 g/mol · KI 166.00 g/mol · PbI₂ 461.0 g/mol)

Amounts of both reactants are given. The theoretical yield comes from the limiting reactant.

Dr. Karmach

Worked example 2 — which reactant limits

Pb(NO₃)₂ + 2 KI → PbI₂ + 2 KNO₃
given: 15.0 g Pb(NO₃)₂ and 12.0 g KI · actual: 14.2 g PbI₂

Four conversion factors are needed: one molar mass for each reactant, then the mole ratio and the product's molar mass.

Step 1 · Compute the theoretical yield

15.0 g Pb(NO₃)₂ × 1 mol Pb(NO₃)₂331.2 g Pb(NO₃)₂ = 0.0453 mol · 12.0 g KI × 1 mol KI166.00 g KI = 0.0723 mol
Dr. Karmach

Worked example 2 — which reactant limits

Pb(NO₃)₂ + 2 KI → PbI₂ + 2 KNO₃
given: 15.0 g Pb(NO₃)₂ and 12.0 g KI · actual: 14.2 g PbI₂
Step 1 · Compute the theoretical yield
15.0 g Pb(NO₃)₂ × 1 mol Pb(NO₃)₂331.2 g Pb(NO₃)₂ = 0.0453 mol · 12.0 g KI × 1 mol KI166.00 g KI = 0.0723 mol
Moles ÷ coefficient: the smaller result marks the limiting reactant.
Pb(NO₃)₂: 0.0453 mol1 = 0.0453 (excess) · KI: 0.0723 mol2 = 0.0362 ← smaller: KI limits
Dr. Karmach

Worked example 2 — which reactant limits

Pb(NO₃)₂ + 2 KI → PbI₂ + 2 KNO₃
given: 15.0 g Pb(NO₃)₂ and 12.0 g KI · actual: 14.2 g PbI₂
Step 1 · Compute the theoretical yield
15.0 g Pb(NO₃)₂ × 1 mol Pb(NO₃)₂331.2 g Pb(NO₃)₂ = 0.0453 mol · 12.0 g KI × 1 mol KI166.00 g KI = 0.0723 mol
Pb(NO₃)₂: 0.0453 mol1 = 0.0453 (excess) · KI: 0.0723 mol2 = 0.0362 ← smaller: KI limits
0.0362 < 0.0453: KI runs out first. The theoretical yield comes from KI alone.
Dr. Karmach

Worked example 2 — the percent yield

Pb(NO₃)₂ + 2 KI → PbI₂ + 2 KNO₃
given: 15.0 g Pb(NO₃)₂ and 12.0 g KI · KI limits, 0.0723 mol · actual: 14.2 g PbI₂

Step 1 · Compute the theoretical yield

0.0723 mol KI × 1 mol PbI₂2 mol KI × 461.0 g PbI₂1 mol PbI₂ = 16.7 g PbI₂ theoretical
Dr. Karmach

Worked example 2 — the percent yield

Pb(NO₃)₂ + 2 KI → PbI₂ + 2 KNO₃
given: 15.0 g Pb(NO₃)₂ and 12.0 g KI · KI limits, 0.0723 mol · actual: 14.2 g PbI₂

Step 1 · Compute the theoretical yield

0.0723 mol KI × 1 mol PbI₂2 mol KI × 461.0 g PbI₂1 mol PbI₂ = 16.7 g PbI₂ theoretical
Step 2 · Take the actual yield from the problem

The dried precipitate weighs 14.2 g. Measured on the balance, not computed.

Dr. Karmach

Worked example 2 — the percent yield

Pb(NO₃)₂ + 2 KI → PbI₂ + 2 KNO₃
given: 15.0 g Pb(NO₃)₂ and 12.0 g KI · KI limits, 0.0723 mol · actual: 14.2 g PbI₂

Step 1 · Compute the theoretical yield

0.0723 mol KI × 1 mol PbI₂2 mol KI × 461.0 g PbI₂1 mol PbI₂ = 16.7 g PbI₂ theoretical
Step 2 · Take the actual yield from the problem Step 3 · Divide: actual ÷ theoretical × 100
14.2 g PbI₂16.7 g PbI₂ × 100 = 85.0%
Dr. Karmach

Worked example 2 — the percent yield

Pb(NO₃)₂ + 2 KI → PbI₂ + 2 KNO₃
given: 15.0 g Pb(NO₃)₂ and 12.0 g KI · KI limits, 0.0723 mol · actual: 14.2 g PbI₂

Step 1 · Compute the theoretical yield

0.0723 mol KI × 1 mol PbI₂2 mol KI × 461.0 g PbI₂1 mol PbI₂ = 16.7 g PbI₂ theoretical
Step 2 · Take the actual yield from the problem Step 3 · Divide: actual ÷ theoretical × 100
14.2 g PbI₂16.7 g PbI₂ × 100 = 85.0%
Below 100% ✓. Some PbI₂ stayed dissolved and some clung to the filter — the balance reads less than the maximum.
Dr. Karmach

Your turn — blast furnace iron

Fe₂O₃ + 3 CO → 2 Fe + 3 CO₂
given: 80.0 g Fe₂O₃, CO in excess · actual: 47.6 g Fe

A furnace run reduces 80.0 g Fe₂O₃ with excess CO and taps 47.6 g of Fe. (Fe₂O₃ 159.70 g/mol · Fe 55.85 g/mol)

80.0 g Fe₂O₃ × 1 mol Fe₂O₃159.70 g Fe₂O₃ × mol Fe mol Fe₂O₃ × 55.85 g Fe1 mol Fe = g Fe
percent yield: 47.6 g Fe g Fe × 100 =

Fill the mole ratio, the theoretical yield, then the percent.

Dr. Karmach

Your turn — blast furnace iron

Fe₂O₃ + 3 CO → 2 Fe + 3 CO₂
given: 80.0 g Fe₂O₃, CO in excess · actual: 47.6 g Fe
80.0 g Fe₂O₃ × 1 mol Fe₂O₃159.70 g Fe₂O₃ × mol Fe mol Fe₂O₃ × 55.85 g Fe1 mol Fe = g Fe
percent yield: 47.6 g Fe g Fe × 100 =
ratio: 2 mol Fe1 mol Fe₂O₃ · theoretical: 56.0 g Fe · 47.6 g Fe56.0 g Fe × 100 = 85.0%
Dr. Karmach

Where this goes wrong

Swapping actual and theoretical. With 14.2 g of PbI₂ collected and 16.7 g possible, 16.7 ÷ 14.2 × 100 = 118%. No experiment beats its maximum; a percent above 100 means the ratio is upside down. Actual goes on top: 14.2 ÷ 16.7 × 100 = 85.0%.
Computing the theoretical yield from the excess reactant. In Pb(NO₃)₂ + 2 KI → PbI₂ + 2 KNO₃, with 15.0 g Pb(NO₃)₂ and 12.0 g KI, the Pb(NO₃)₂ chain gives 20.9 g and 14.2 ÷ 20.9 × 100 = 68.0%. KI runs out first: the maximum is 16.7 g and the yield is 85.0%.
Comparing product to starting material. In CaCO₃ → CaO + CO₂, 18.5 g of CO₂ from 50.0 g of CaCO₃ suggests 18.5 ÷ 50.0 × 100 = 37.0%. The 100% mark is the 22.0 g of CO₂ stoichiometry allows, and the yield is 84.1%.
Reporting the fraction as the percent. 18.5 ÷ 22.0 = 0.841 is a fraction of the maximum. Multiplied by 100 it becomes the percent yield, 84.1%. An answer of 0.841% would mean nearly everything was lost.
Dr. Karmach

Practice 1

2 H₂O₂ → 2 H₂O + O₂

A bottle of hydrogen peroxide decomposes completely. From 40.0 g of H₂O₂, 15.6 g of O₂ is collected. What is the percent yield? (H₂O₂ 34.02 g/mol · O₂ 32.00 g/mol)

  1. 39.0%
  2. 83.0%
  3. 0.830
  4. 41.5%
Dr. Karmach

Practice 1 — answer: B

2 H₂O₂ → 2 H₂O + O₂
given: 40.0 g H₂O₂ · actual: 15.6 g O₂
40.0 g H₂O₂ × 1 mol H₂O₂34.02 g H₂O₂ × 1 mol O₂2 mol H₂O₂ × 32.00 g O₂1 mol O₂ = 18.8 g O₂ theoretical
15.6 g O₂18.8 g O₂ × 100 = 83.0% — answer B

A compared product to starting material: 15.6/40.0 × 100 = 39.0. C left the fraction as a decimal: 15.6/18.8 = 0.830. D skipped the mole ratio in the theoretical yield: 40.0/34.02 × 32.00 = 37.6 g, then 15.6/37.6 × 100 = 41.5.

Dr. Karmach

Practice 1 — answer: B

2 H₂O₂ → 2 H₂O + O₂
given: 40.0 g H₂O₂ · actual: 15.6 g O₂
40.0 g H₂O₂ × 1 mol H₂O₂34.02 g H₂O₂ × 1 mol O₂2 mol H₂O₂ × 32.00 g O₂1 mol O₂ = 18.8 g O₂ theoretical
15.6 g O₂18.8 g O₂ × 100 = 83.0% — answer B
The product is a gas, and some escapes collection. 83 g reached the flask for every 100 g possible. Below 100% ✓
Dr. Karmach

Any two of the three determine the third

percent yield = actual ÷ theoretical × 100
a stated percent links the two masses: 78.0% yield — 78.0 g actual per 100 g theoretical

Written as a fraction, a stated percent yield converts between actual and theoretical grams in either direction. Given any two of the three quantities, the relation gives the third.

Dr. Karmach

Worked example 3 — reactant mass from a stated yield

Zn + 2 HCl → ZnCl₂ + H₂
wanted: 5.00 g ZnCl₂ actual · typical yield: 78.0% · find: g Zn

This preparation typically delivers a 78.0% yield. A procedure calls for 5.00 g of ZnCl₂, collected and dried. What mass of zinc must be weighed out? (Zn 65.38 g/mol · ZnCl₂ 136.28 g/mol)

Find the theoretical yield first, then the mass of Zn that provides it.

Dr. Karmach

Worked example 3 — solution

Zn + 2 HCl → ZnCl₂ + H₂
wanted: 5.00 g ZnCl₂ actual · typical yield: 78.0% · find: g Zn

Four conversion factors are needed: the percent yield, then the mass-to-mass chain run from product to reactant.

Theoretical yield required

At 78.0% yield, every 100 g theoretical delivers 78.0 g actual. Two orientations exist. Only one cancels the given g actual:

100 g theoretical78.0 g actual cancels g actual ✓    78.0 g actual100 g theoretical cancels nothing ✗
Dr. Karmach

Worked example 3 — solution

Zn + 2 HCl → ZnCl₂ + H₂
wanted: 5.00 g ZnCl₂ actual · typical yield: 78.0% · find: g Zn
Theoretical yield required
5.00 g actual × 100 g theoretical78.0 g actual = 6.41 g ZnCl₂ theoretical
Dr. Karmach

Worked example 3 — solution

Zn + 2 HCl → ZnCl₂ + H₂
wanted: 5.00 g ZnCl₂ actual · typical yield: 78.0% · find: g Zn
Theoretical yield required
5.00 g actual × 100 g theoretical78.0 g actual = 6.41 g ZnCl₂ theoretical
Mass-to-mass, product to reactant
6.41 g ZnCl₂ × 1 mol ZnCl₂136.28 g ZnCl₂ × 1 mol Zn1 mol ZnCl₂ × 65.38 g Zn1 mol Zn = 3.08 g Zn
Dr. Karmach

Worked example 3 — solution

Zn + 2 HCl → ZnCl₂ + H₂
wanted: 5.00 g ZnCl₂ actual · typical yield: 78.0% · find: g Zn
Theoretical yield required
5.00 g actual × 100 g theoretical78.0 g actual = 6.41 g ZnCl₂ theoretical
Mass-to-mass, product to reactant
6.41 g ZnCl₂ × 1 mol ZnCl₂136.28 g ZnCl₂ × 1 mol Zn1 mol ZnCl₂ × 65.38 g Zn1 mol Zn = 3.08 g Zn
The theoretical target, 6.41 g, exceeds the 5.00 g needed: a 78.0% yield loses 22 g of every 100. Weighing out 3.08 g of Zn covers the loss. ✓
Dr. Karmach

Practice 2

N₂ + 3 H₂ → 2 NH₃

A reactor is charged with 30.0 g N₂ and 10.0 g H₂ and delivers 22.6 g of NH₃. What is the percent yield? (N₂ 28.02 g/mol · H₂ 2.016 g/mol · NH₃ 17.03 g/mol)

  1. 61.9%
  2. 40.1%
  3. 56.5%
  4. 0.619
Dr. Karmach

Practice 2 — answer: A

N₂ + 3 H₂ → 2 NH₃ · given: 30.0 g N₂ and 10.0 g H₂
N₂: 1.07 mol1 = 1.07 ← smaller: N₂ limits · H₂: 4.96 mol3 = 1.65 (excess)
30.0 g N₂ × 1 mol N₂28.02 g N₂ × 2 mol NH₃1 mol N₂ × 17.03 g NH₃1 mol NH₃ = 36.5 g theoretical
22.6 g NH₃36.5 g NH₃ × 100 = 61.9% — answer A
Dr. Karmach

Practice 2 — answer: A

N₂ + 3 H₂ → 2 NH₃ · given: 30.0 g N₂ and 10.0 g H₂
N₂: 1.07 mol1 = 1.07 ← smaller: N₂ limits · H₂: 4.96 mol3 = 1.65 (excess)
30.0 g N₂ × 1 mol N₂28.02 g N₂ × 2 mol NH₃1 mol N₂ × 17.03 g NH₃1 mol NH₃ = 36.5 g theoretical
22.6 g NH₃36.5 g NH₃ × 100 = 61.9% — answer A
B used excess H₂: 22.6/56.3 × 100 = 40.1. C divided by 40.0 g loaded: 22.6/40.0 × 100 = 56.5. D left the decimal: 22.6/36.5 = 0.619.
Dr. Karmach

Practice 2 — answer: A

N₂ + 3 H₂ → 2 NH₃ · given: 30.0 g N₂ and 10.0 g H₂
N₂: 1.07 mol1 = 1.07 ← smaller: N₂ limits · H₂: 4.96 mol3 = 1.65 (excess)
30.0 g N₂ × 1 mol N₂28.02 g N₂ × 2 mol NH₃1 mol N₂ × 17.03 g NH₃1 mol NH₃ = 36.5 g theoretical
22.6 g NH₃36.5 g NH₃ × 100 = 61.9% — answer A
Below 100% ✓. The maximum comes from the limiting N₂, not from the excess H₂.
Dr. Karmach

Check yourself

  1. Percent yield divides two masses. Which is computed, and which is read from the balance? (Which substance do both refer to?)
  2. Masses of two reactants are given, plus the product mass collected. List the steps from the given data to the percent yield. (Which reactant sets the 100% mark?)

A balanced equation predicts one more product: energy. A reaction releases or absorbs a fixed amount per mole, and the same conversion-factor chains count it — in joules instead of grams.

Dr. Karmach

Can you…?

  • ☐ balance any chemical equation with the smallest whole-number coefficients?
  • ☐ read a balanced equation as a recipe: coefficients are mole relationships?
  • ☐ convert between amounts of any two species using mole ratios?
  • ☐ chain molar masses with mole ratios to solve gram-to-gram problems?
  • ☐ identify which reactant limits a reaction and how much product it allows?
  • ☐ classify a reaction by type and cite the evidence that a reaction occurred?
  • ☐ apply the solubility rules to predict precipitates and assign physical states?
  • ☐ write molecular, complete ionic, and net ionic equations and classify electrolytes?
  • ☐ assign oxidation numbers and identify oxidizing and reducing agents?
  • ☐ carry molarity through stoichiometric calculations and compute percent yield?

If any box stays empty, the practice site has a drill for it. 🧪

Dr. Karmach

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