AP Chemistry

AP Chemistry Unit 7 review: Equilibrium

Unit 7 describes reversible reactions at equilibrium and how composition responds to a disturbance. It is 7–9% of multiple choice. Expect to compare Q with K, calculate equilibrium amounts and explain shifts with particle-level reasoning rather than a memorized slogan.

Unit 7 on the May 2027 exam

AP Chemistry Unit 7 exam facts
2027 exam
Weight7–9% of the multiple-choice section
Exam dateThursday, May 6, 2027, afternoon session
Multiple choice60 questions in 90 minutes, worth 50% of the exam score
Free response7 questions in 105 minutes, worth 50%: three long questions (10 points each) and four short questions (4 points each).
CalculatorBoth sections allow scientific or approved graphing calculators. Four-function calculators are allowed but not recommended. Bluebook includes both Desmos scientific and graphing calculators.
Class timeAbout 13–15 class periods in College Board's pacing guide
2026 results15% of students scored a 5 on the whole exam, and about 76% scored 3 or higher

Sources: College Board's course and exam description, exam page, 2027 exam dates and score distributions.

What Unit 7 covers

College Board's course description splits the unit into 12 topics. The second column is what you should be able to do for each one.

AP Chemistry Unit 7 topics
TopicWhat you should be able to do
7.1 Introduction to EquilibriumExplain dynamic equilibrium as equal forward and reverse rates with constant macroscopic composition.
7.2 Direction of Reversible ReactionsPredict the direction of net reaction from relative forward and reverse rates.
7.3 Reaction Quotient and Equilibrium ConstantConstruct Q and K expressions with coefficients as exponents and appropriate phases omitted.
7.4 Calculating the Equilibrium ConstantCalculate K from measured equilibrium concentrations or partial pressures.
7.5 Magnitude of the Equilibrium ConstantInterpret large and small K values without confusing equilibrium position with reaction speed.
7.6 Properties of the Equilibrium ConstantTransform K when a reaction is reversed, multiplied or combined with another reaction.
7.7 Calculating Equilibrium ConcentrationsSet up initial, change and equilibrium amounts and solve for unknown concentrations.
7.8 Representations of EquilibriumConnect particle diagrams and concentration graphs to equilibrium composition.
7.9 Introduction to Le Châtelier’s PrinciplePredict responses to concentration, pressure, volume and temperature changes.
7.10 Reaction Quotient and Le Châtelier’s PrincipleJustify a shift by showing how the disturbance changes Q relative to K.
7.11 Introduction to Solubility EquilibriaWrite solubility-product expressions and connect Ksp to molar solubility.
7.12 Common-Ion EffectCalculate or explain the effect of an added common ion on solubility.

Q and K tell you direction; the equation tells you the amount

Use the same reaction and expression for both Q and K. Temperature fixes K for that reaction.

Q and K tell you direction; the equation tells you the amount
Condition or operationResultReason
Q < KNet forward reactionProduct-to-reactant activity ratio must increase.
Q > KNet reverse reactionProduct-to-reactant activity ratio must decrease.
Q = KEquilibriumForward and reverse rates are equal, not zero.
Reverse the equationKnew = 1/KNumerator and denominator exchange.
Multiply coefficients by nKnew = KⁿEvery exponent is multiplied by n.
Add reaction equationsKoverall = K₁K₂Equilibrium expressions multiply and shared species cancel.
Add a common ionMolar solubility usually decreasesThe ion raises Qsp; precipitation restores Qsp = Ksp.
Add a catalystK and equilibrium composition stay the sameThe system approaches equilibrium faster.

Common mistakes

Each of these loses points on questions you otherwise understand.

  • Treating equilibrium as stopped reactions or equal concentrations. The rates are equal; reactant and product concentrations may differ. CED topic 7.1.
  • Ignoring a very large K when choosing an approximation. A product-favored reaction may be nearly complete, so an assumption of tiny conversion can fail. CED printed p. 125 highlights this problem.
  • Including a pure solid or pure liquid in a standard equilibrium expression. Its activity is fixed in the model. CED topic 7.3.
  • Assuming pressure always shifts a gas equilibrium. Compare gaseous stoichiometric totals and explain how Q changes; equal totals give no compression-driven shift in the ideal model. CED topics 7.9–7.10.

6 practice questions with answers

Written by Ashore for this page, in the style of the multiple-choice section. Try each one before you open the answer.

  1. Question 1 · 7.4

    For A(g) ⇌ 2B(g), equilibrium concentrations are [A] = 0.200 M and [B] = 0.300 M. What is Kc?

    • A0.667
    • B1.50
    • C0.450
    • D2.25
    Show the answer

    C. Kc = [B]²/[A] = (0.300)²/0.200 = 0.450. The coefficient 2 becomes an exponent, not a factor multiplying [B].

  2. Question 2 · 7.10

    For A ⇌ B, K = 4.0. A mixture has [A] = 0.50 M and [B] = 1.0 M. Which change occurs as equilibrium is approached?

    • ANet conversion of A to B
    • BNet conversion of B to A
    • CNo net reaction because Q = K
    • DK decreases until it equals Q
    Show the answer

    A. Q = [B]/[A] = 1.0/0.50 = 2.0. Since Q < K, the forward reaction increases the ratio toward 4.0. At fixed temperature, K does not adjust to the initial mixture.

  3. Question 3 · 7.6

    The reaction A ⇌ B has K = 9.0. What is K for 2B ⇌ 2A at the same temperature?

    • A18
    • B81
    • C1/18
    • D1/81
    Show the answer

    D. Reversing gives 1/9. Doubling all coefficients squares that value: (1/9)² = 1/81. Doubling a reaction does not merely double K.

  4. Question 4 · 7.7

    Initially [A] = 0.600 M and [B] = 0 in A ⇌ B at constant volume. If K = 2.00, what is [B] at equilibrium?

    • A0.200 M
    • B0.400 M
    • C0.300 M
    • D0.600 M
    Show the answer

    B. Let x M of A convert to B. Then K = x/(0.600 − x) = 2.00. Solving x = 1.200 − 2x gives x = 0.400 M, leaving [A] = 0.200 M.

  5. Question 5 · 7.11

    For MX₂(s) ⇌ M²⁺ + 2X⁻, Ksp = 1.08 × 10⁻¹⁰. What is the molar solubility in pure water?

    • A1.04 × 10⁻⁵ M
    • B4.76 × 10⁻⁴ M
    • C3.00 × 10⁻⁴ M
    • D1.08 × 10⁻¹⁰ M
    Show the answer

    C. If solubility is s, [M²⁺] = s and [X⁻] = 2s. Ksp = s(2s)² = 4s³. Thus s³ = 2.70 × 10⁻¹¹ and s = 3.00 × 10⁻⁴ M.

  6. Question 6 · 7.12

    AgCl has Ksp = 1.8 × 10⁻¹⁰. In 0.020 M NaCl, neglecting added chloride from dissolution, what is [Ag⁺] at saturation?

    • A9.0 × 10⁻⁹ M
    • B3.6 × 10⁻¹² M
    • C1.3 × 10⁻⁵ M
    • D9.0 × 10⁻⁷ M
    Show the answer

    A. Ksp = [Ag⁺][Cl⁻], so [Ag⁺] = 1.8 × 10⁻¹⁰/0.020 = 9.0 × 10⁻⁹ M. This is much smaller than 0.020 M, consistent with neglecting the extra chloride.

How to study Unit 7

For each disturbance, write the expression for Q and mark which term changes immediately. Compare that new Q with unchanged K unless temperature changes. Only then state the net reaction direction.

For an equilibrium calculation, define x and write the stoichiometric changes before solving. Substitute the answer into the original K expression and check that no concentration is negative. For solubility, derive every ion concentration from the dissolution equation rather than setting all of them equal to s.

Ashore's Chemistry course has a short lesson for every topic in this unit, each ending with a few questions on what it taught.

Questions

Still have a question? support@tryashore.com

It is 7–9% of the multiple-choice section, which is half the exam score. This is not a fixed share of the whole exam: free-response questions can combine units. Suggested pacing is 13–15 class periods.

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Starting check

SAT Math · 1 of 5

Calculator allowed

A jacket's price is increased by 20% and then the new price is decreased by 20%. The final price is what percent of the original price?
  • A96%96\%
  • B100%100\%
  • C104%104\%
  • D80%80\%