Lesson 3 of 4
Equilibrium expressions and calculations
Use equilibrium concentrations or partial pressures, with stoichiometry to find missing amounts.
A-Level 9476 (2026-2027)
I can deduce concentration and partial-pressure expressions.Syllabus
Syllabus 9476, 9(d). Deduce concentration and partial-pressure expressions.
I can calculate Kc or Kp from equilibrium data.Syllabus
Syllabus 9476, 9(e). Calculate Kc or Kp from equilibrium data.
I can calculate quantities present at equilibrium.Syllabus
Syllabus 9476, 9(f). Calculate quantities present at equilibrium.
Build K from the written equation and equilibrium quantities
Products go above reactants; stoichiometric coefficients become powers.
For aA + bB ⇌ cC + dD, the concentration expression is Kc = [C]c[D]d / ([A]a[B]b), using equilibrium concentrations. Kp uses equilibrium partial pressures of gaseous species in the same pattern. Pure solids and pure liquids are omitted because their activities are constant; a dissolved species is not omitted merely because it is in a liquid solution.
| Reaction | Expression |
|---|---|
| H2(g) + I2(g) ⇌ 2HI(g) | Kc = [HI]2 / ([H2][I2]); Kp = p(HI)2 / (p(H2)p(I2)). |
| N2(g) + 3H2(g) ⇌ 2NH3(g) | Kc = [NH3]2 / ([N2][H2]3); Kp = p(NH3)2 / (p(N2)p(H2)3). |
| CaCO3(s) ⇌ CaO(s) + CO2(g) | Kp = p(CO2), with both pure solid phases present. |
| CH3COOH(aq) + C2H5OH(aq) ⇌ CH3COOC2H5(aq) + H2O(l) | In a dilute aqueous treatment, water as the solvent is incorporated into the constant; retain the dissolved reacting species. Read the stated medium. |
In conventional examination expressions, derive any units from the concentration or pressure powers and use one consistent pressure unit. For N2O4(g) ⇌ 2NO2(g), the concentration expression has units mol dm-3 and a pressure expression in kPa has units kPa. The numerical pressure-based value changes if the pressure unit changes, so report the unit used.
Worked exampleFind Kp from a gas mixture
At equilibrium, a mixture contains 0.0200 mol N2O4 and 0.0400 mol NO2 at total pressure 150 kPa. Calculate Kp for N2O4 ⇌ 2NO2.
Try it first. Then show the worked stepsHide the worked steps
- Total gas amount = 0.0600 mol.
- p(N2O4) = (0.0200/0.0600)(150) = 50.0 kPa; p(NO2) = 100 kPa.
- Kp = p(NO2)2 / p(N2O4) = 1002/50.0.
Kp = 200 kPa for the stated pressure convention and temperature.
Try it step by step
Work it out in steps: Total amount of gas, then Partial pressure of N2O4, then Kp = p(NO2)2 / p(N2O4).
Show the answer
Problem 1.
Total amount of gas: Total = 0.100 + 0.200 = 0.300 mol.
Partial pressure of N2O4: p(N2O4) = (0.100/0.300) x 300 = 100 kPa, and p(NO2) = 200 kPa.
Kp = p(NO2)2 / p(N2O4): Kp = 2002 / 100 = 400 kPa.
Problem 2.
Total amount of gas: Total = 0.400 mol.
Partial pressure of N2O4: p(N2O4) = (0.300/0.400) x 200 = 150 kPa, and p(NO2) = 50.0 kPa.
Kp = p(NO2)2 / p(N2O4): Kp = 50.02 / 150 = 16.7 kPa.
Problem 3.
Total amount of gas: Total = 0.0500 + 0.150 = 0.200 mol.
Partial pressure of N2O4: p(N2O4) = (0.0500/0.200) x 120 = 30.0 kPa, and p(NO2) = 90.0 kPa.
Kp = p(NO2)2 / p(N2O4): Kp = 90.02 / 30.0 = 270 kPa.
Reversing a reaction takes the reciprocal of K; multiplying all coefficients by a factor raises K to that power. A large K favours products relative to reactants in its expression, but gives no direct information about the speed of reaching equilibrium. The relationship converting Kp into Kc is not required in this syllabus.
Use stoichiometry to complete the equilibrium row
Amounts change in the coefficient ratio before they are converted to concentration or partial pressure.
Worked exampleCalculate Kc from an observed equilibrium amount
A 1.00 dm3 vessel initially contains 0.100 mol H2 and 0.100 mol I2, with no HI. At equilibrium, it contains 0.160 mol HI. Find Kc for H2 + I2 ⇌ 2HI.
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- Forming 0.160 mol HI consumes 0.0800 mol H2 and 0.0800 mol I2.
- Equilibrium amounts are 0.0200, 0.0200 and 0.160 mol respectively.
- Divide each amount by 1.00 dm3 to obtain the equilibrium concentrations.
- Kc = 0.1602/(0.0200 × 0.0200).
Kc = 64.0, with no net concentration unit for this expression.
Try it step by step
Work it out in steps: Amount of reactant used up, then Equilibrium amount of reactant, then Kc.
Show the answer
Problem 1.
Amount of reactant used up: Forming 0.600 mol HI uses 0.300 mol H2 and 0.300 mol I2 (ratio 1 : 1 : 2).
Equilibrium amount of reactant: Equilibrium H2 = I2 = 0.400 - 0.300 = 0.100 mol. Divide by 2.00 dm3: [H2] = [I2] = 0.0500 and [HI] = 0.300 mol dm-3.
Kc: Kc = 0.3002 / (0.0500 x 0.0500) = 36.0. The units cancel for this equation.
Problem 2.
Amount of reactant used up: Forming 0.200 mol Cl2 uses 0.200 mol PCl5 and also forms 0.200 mol PCl3.
Equilibrium amount of reactant: Equilibrium PCl5 = 0.500 - 0.200 = 0.300 mol, so [PCl5] = 0.300, [PCl3] = [Cl2] = 0.200 mol dm-3.
Kc: Kc = (0.200 x 0.200) / 0.300 = 0.133 mol dm-3.
Problem 3.
Amount of reactant used up: Forming 0.400 mol NO2 uses 0.400 / 2 = 0.200 mol N2O4.
Equilibrium amount of reactant: Equilibrium N2O4 = 1.00 - 0.200 = 0.800 mol, so [N2O4] = 0.400 and [NO2] = 0.200 mol dm-3.
Kc: Kc = 0.2002 / 0.400 = 0.100 mol dm-3.
| Stage | H2 / mol | I2 / mol | HI / mol |
|---|---|---|---|
| Initial | 0.100 | 0.100 | 0 |
| Change | -x | -x | +2x |
| Equilibrium | 0.100 - x | 0.100 - x | 2x |
Worked exampleFind the equilibrium composition from K
For the same initial amounts in 1.00 dm3, suppose Kc = 64.0 is supplied instead. Calculate the equilibrium amounts without solving a quadratic.
Try it first. Then show the worked stepsHide the worked steps
- Substitute the equilibrium expressions: 64 = (2x)2/(0.100 - x)2.
- Concentrations are positive, so take the positive square root: 8 = 2x/(0.100 - x).
- 8(0.100 - x) = 2x; hence x = 0.0800 mol.
- Substitute back and check that no amount is negative.
H2 = I2 = 0.0200 mol and HI = 0.160 mol. Substitution into K verifies the result.
A useful table is not a substitute for checking the chemistry. Include any initial product, account for unequal coefficients, and use the actual equilibrium volume. When gaseous mole number changes, total pressure cannot be split using initial mole fractions. The required syllabus calculations do not need quadratic-equation solutions.