AP Chemistry Equilibrium — Complete Guide with Practice Problems (2026)
Chemical equilibrium is one of the highest-weighted topics on AP Chemistry, appearing in both multiple choice and FRQ sections every year. This guide covers every equilibrium concept tested on the AP exam, with worked examples and practice problems.
What Is Chemical Equilibrium?
A reaction reaches equilibrium when the rate of the forward reaction equals the rate of the reverse reaction. At this point, the concentrations of reactants and products remain constant — but the reaction has not stopped. It is a dynamic equilibrium.
$$\text{reactants} \rightleftharpoons \text{products}$$
Key point: Equilibrium does not mean equal concentrations. It means the rate of forward = rate of reverse.
The Equilibrium Constant (Keq)
For a generic reaction: $aA + bB \rightleftharpoons cC + dD$
$$K_{eq} = \frac{[C]^c[D]^d}{[A]^a[B]^b}$$
Rules for writing K expressions:
- Use molar concentrations (mol/L) for aqueous species and gases
- Pure solids and pure liquids are NOT included in K expressions (their concentration is constant)
- Coefficients in the balanced equation become exponents in K
Example: Write Keq for $\text{N}_2(g) + 3\text{H}_2(g) \rightleftharpoons 2\text{NH}_3(g)$
$$K_c = \frac{[\text{NH}_3]^2}{[\text{N}_2][\text{H}_2]^3}$$
Interpreting K Values
| K value | Meaning |
|---|---|
| K >> 1 | Products favored; reaction essentially goes to completion |
| K << 1 | Reactants favored; very little product forms |
| K ≈ 1 | Significant amounts of both reactants and products at equilibrium |
Kp vs Kc
Kc uses molar concentrations (mol/L). Kp uses partial pressures (atm).
$$K_p = K_c(RT)^{\Delta n}$$
Where $\Delta n$ = moles of gaseous products − moles of gaseous reactants, R = 0.08206 L·atm/mol·K, T = temperature in Kelvin.
Example: For $\text{N}_2(g) + 3\text{H}_2(g) \rightleftharpoons 2\text{NH}_3(g)$
$\Delta n = 2 - (1 + 3) = -2$
$$K_p = K_c(RT)^{-2} = \frac{K_c}{(RT)^2}$$
The Reaction Quotient Q
Q has the same form as K, but uses current concentrations (not equilibrium concentrations).
| Comparison | Meaning | Direction reaction shifts |
|---|---|---|
| Q < K | Too many reactants | Forward (→ toward products) |
| Q > K | Too many products | Reverse (← toward reactants) |
| Q = K | At equilibrium | No shift |
AP exam tip: Q vs K problems are extremely common. Always state which direction the reaction shifts and why.
ICE Tables
ICE (Initial, Change, Equilibrium) tables are the standard method for calculating equilibrium concentrations.
Example: 0.500 mol of N₂ and 0.500 mol of H₂ are placed in a 1.00 L container. At equilibrium, [NH₃] = 0.060 M. Find Kc.
Reaction: $\text{N}_2 + 3\text{H}_2 \rightleftharpoons 2\text{NH}_3$
| N₂ | H₂ | NH₃ | |
|---|---|---|---|
| I | 0.500 | 0.500 | 0 |
| C | −x | −3x | +2x |
| E | 0.500−x | 0.500−3x | 2x |
Given: $2x = 0.060 \Rightarrow x = 0.030$
$[\text{N}_2] = 0.500 - 0.030 = 0.470$ M $[\text{H}_2] = 0.500 - 0.090 = 0.410$ M $[\text{NH}_3] = 0.060$ M
$$K_c = \frac{(0.060)^2}{(0.470)(0.410)^3} = \frac{0.0036}{0.0324} = \boxed{0.111}$$
Le Chatelier's Principle
If a system at equilibrium is disturbed, it will shift to minimize the disturbance and re-establish equilibrium.
Concentration Changes
| Change | Shift direction |
|---|---|
| Add reactant | Forward (→) |
| Remove reactant | Reverse (←) |
| Add product | Reverse (←) |
| Remove product | Forward (→) |
Pressure/Volume Changes (Gas-phase reactions only)
| Change | Effect | Shift |
|---|---|---|
| Increase pressure (decrease V) | Shift toward fewer moles of gas | |
| Decrease pressure (increase V) | Shift toward more moles of gas | |
| Add inert gas at constant V | No effect on equilibrium |
Example: $\text{N}_2(g) + 3\text{H}_2(g) \rightleftharpoons 2\text{NH}_3(g)$
Increasing pressure shifts toward the side with fewer moles of gas: products (2 moles vs 4 moles). Reaction shifts forward → more NH₃ produced.
Temperature Changes
| Change | Effect on K | Exothermic rxn shift | Endothermic rxn shift |
|---|---|---|---|
| Increase T | K changes | Reverse (←) | Forward (→) |
| Decrease T | K changes | Forward (→) | Reverse (←) |
Key distinction: Concentration and pressure changes shift equilibrium but do NOT change K. Temperature changes shift equilibrium AND change K.
Gases in Equilibrium — Partial Pressures
For gas-phase equilibria, you can use partial pressures directly in Kp expressions.
Dalton's Law: $P_{total} = P_A + P_B + P_C + \cdots$
Mole fraction: $\chi_A = \frac{n_A}{n_{total}}$, then $P_A = \chi_A \cdot P_{total}$
Example FRQ-style: A mixture of 0.40 atm SO₂, 0.20 atm O₂, and 0.80 atm SO₃ is placed in a container.
Reaction: $2\text{SO}_2(g) + \text{O}_2(g) \rightleftharpoons 2\text{SO}_3(g)$ with $K_p = 1.7 \times 10^2$
$$Q_p = \frac{(P_{\text{SO}3})^2}{(P{\text{SO}2})^2(P{\text{O}_2})} = \frac{(0.80)^2}{(0.40)^2(0.20)} = \frac{0.64}{0.032} = 20$$
Since $Q_p (20) < K_p (170)$, the reaction shifts forward to produce more SO₃.
Solubility Equilibrium (Ksp)
When a slightly soluble ionic compound dissolves:
$$\text{AB}(s) \rightleftharpoons \text{A}^+(aq) + \text{B}^-(aq)$$ $$K_{sp} = [\text{A}^+][\text{B}^-]$$
The solid is not included in Ksp because it's a pure solid.
Common Ksp expressions:
| Compound | Dissolution | Ksp expression |
|---|---|---|
| AgCl | $\text{AgCl} \rightleftharpoons \text{Ag}^+ + \text{Cl}^-$ | $K_{sp} = [\text{Ag}^+][\text{Cl}^-]$ |
| PbCl₂ | $\text{PbCl}_2 \rightleftharpoons \text{Pb}^{2+} + 2\text{Cl}^-$ | $K_{sp} = [\text{Pb}^{2+}][\text{Cl}^-]^2$ |
| Ca₃(PO₄)₂ | $\rightleftharpoons 3\text{Ca}^{2+} + 2\text{PO}_4^{3-}$ | $K_{sp} = [\text{Ca}^{2+}]^3[\text{PO}_4^{3-}]^2$ |
Will a Precipitate Form?
Compare the ion product Q to Ksp:
- Q > Ksp → precipitate forms (solution is supersaturated)
- Q < Ksp → no precipitate (solution is unsaturated)
- Q = Ksp → at saturation
AP Chemistry Equilibrium Practice Problems
Problem 1: For the reaction $\text{H}_2(g) + \text{I}_2(g) \rightleftharpoons 2\text{HI}(g)$, Kc = 54.3 at 430°C. If [H₂] = [I₂] = 0.10 M and [HI] = 0.50 M, which direction does the reaction shift?
$Q = \frac{(0.50)^2}{(0.10)(0.10)} = \frac{0.25}{0.01} = 25$. Since Q (25) < K (54.3), reaction shifts forward.
Problem 2: The Ksp of BaSO₄ is 1.1 × 10⁻¹⁰. What is the molar solubility of BaSO₄?
$\text{BaSO}_4 \rightleftharpoons \text{Ba}^{2+} + \text{SO}4^{2-}$ Let solubility = s. Then $K{sp} = s \cdot s = s^2$ $s = \sqrt{1.1 \times 10^{-10}} = 1.05 \times 10^{-5}$ mol/L
Problem 3: If the temperature is raised for an endothermic reaction at equilibrium, what happens to K and to the equilibrium position?
K increases (temperature change always changes K). The equilibrium shifts forward (toward products), consistent with the higher K.
How Equilibrium Is Tested on AP Chemistry FRQs
Equilibrium appears on nearly every AP Chemistry FRQ section. Common question types:
- Write the Kc or Kp expression for a given reaction
- Use an ICE table to find equilibrium concentrations
- Calculate Q and determine shift direction
- Apply Le Chatelier's principle to predict the effect of a change
- Calculate molar solubility from Ksp or vice versa
- Determine whether a precipitate forms given ion concentrations
AP reader expectation: Show your ICE table. Label rows clearly (I, C, E). Show algebraic setup before plugging in numbers.