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How do we quantify the position of equilibrium, and what changes its value?

The equilibrium constant Kc in terms of concentrations and Kp in terms of partial pressures and mole fractions, calculations from equilibrium amounts, and the effect of temperature and catalysts on the constant.

An OCR H432 module 5 answer on equilibrium constants: writing and calculating Kc from concentrations and Kp from partial pressures and mole fractions, and the effect of temperature and catalysts on the value of the constant.

Generated by Claude Opus 4.812 min answer

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  1. What this topic is asking
  2. The equilibrium constant Kc
  3. The equilibrium constant Kp
  4. What changes the constant
  5. Examples in context
  6. Try this

What this topic is asking

OCR specification point 5.1.2 wants you to write the equilibrium constant KcK_c in terms of concentrations and KpK_p in terms of partial pressures, calculate them from equilibrium amounts (using mole fractions for KpK_p), deduce their units, and state how temperature changes the constant while a catalyst does not. This puts numbers on the Le Chatelier ideas of Module 3.

The equilibrium constant Kc

To calculate KcK_c: find the equilibrium amounts (often from an initial-change-equilibrium table), convert to concentrations by dividing by the volume, substitute into the expression, and work out the units by cancelling.

The equilibrium constant Kp

The mole fraction of a gas is its moles divided by the total moles of gas. The partial pressures must add up to the total pressure.

What changes the constant

Examples in context

Example 1. The Haber process compromise. A high pressure raises the equilibrium yield of ammonia (fewer gas moles on the product side) but does not change KpK_p; the moderate temperature used is a compromise between a higher yield (favoured by low temperature, since the forward reaction is exothermic) and a workable rate.

Example 2. Why KK alone does not give the rate. A large KcK_c means the equilibrium lies well towards products, but says nothing about how fast equilibrium is reached, which is why a separate catalyst is used in industrial processes.

Try this

Q1. Write the expression for KcK_c for 2NO2(g)N2O4(g)2\text{NO}_2(g) \rightleftharpoons \text{N}_2\text{O}_4(g). [1 mark]

  • Cue. Kc=[N2O4][NO2]2K_c = \dfrac{[\text{N}_2\text{O}_4]}{[\text{NO}_2]^2}.

Q2. State the only factor that changes the value of KpK_p. [1 mark]

  • Cue. Temperature.

Exam-style practice questions

Practice questions written in the style of OCR exam questions on this dot point, with worked answer explainers. The year tag is the paper they imitate, not the source.

OCR 20204 marksFor the equilibrium H2(g)+I2(g)2HI(g)\text{H}_2(g) + \text{I}_2(g) \rightleftharpoons 2\text{HI}(g), an equilibrium mixture in a 1.0 dm31.0\ \text{dm}^3 vessel contains 0.20 mol0.20\ \text{mol} H2\text{H}_2, 0.20 mol0.20\ \text{mol} I2\text{I}_2 and 1.60 mol1.60\ \text{mol} HI\text{HI}. (a) Write the expression for KcK_c. (b) Calculate KcK_c and state its units.
Show worked answer →

(a) Kc=[HI]2[H2][I2]K_c = \dfrac{[\text{HI}]^2}{[\text{H}_2][\text{I}_2]} (1).

(b) Concentrations equal moles here (volume 1.0 dm31.0\ \text{dm}^3). Kc=(1.60)2(0.20)(0.20)=2.560.040=64K_c = \dfrac{(1.60)^2}{(0.20)(0.20)} = \dfrac{2.56}{0.040} = 64 (1)(1). The units cancel ((mol dm3)2(mol dm3)2\frac{(\text{mol dm}^{-3})^2}{(\text{mol dm}^{-3})^2}), so KcK_c has no units (1).

Markers reward the correct expression, the substituted values, the value 6464, and the recognition that the units cancel.

OCR 20224 marksFor N2O4(g)2NO2(g)\text{N}_2\text{O}_4(g) \rightleftharpoons 2\text{NO}_2(g) at equilibrium the total pressure is 100 kPa100\ \text{kPa} and the mole fraction of NO2\text{NO}_2 is 0.400.40. (a) Find the partial pressures. (b) Write and evaluate KpK_p.
Show worked answer →

(a) Mole fraction of N2O4=10.40=0.60\text{N}_2\text{O}_4 = 1 - 0.40 = 0.60. Partial pressures: p(NO2)=0.40×100=40 kPap(\text{NO}_2) = 0.40 \times 100 = 40\ \text{kPa} and p(N2O4)=0.60×100=60 kPap(\text{N}_2\text{O}_4) = 0.60 \times 100 = 60\ \text{kPa} (1)(1).

(b) Kp=p(NO2)2p(N2O4)=(40)260=160060=27 kPaK_p = \dfrac{p(\text{NO}_2)^2}{p(\text{N}_2\text{O}_4)} = \dfrac{(40)^2}{60} = \dfrac{1600}{60} = 27\ \text{kPa} (1)(1).

Markers reward both partial pressures from the mole fractions, the correct KpK_p expression, the value, and the units kPa\text{kPa}.

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