How do reversible reactions settle into balance, and how do we measure that balance?
Dynamic equilibrium, Le Chatelier's principle and the effect of changing concentration, pressure and temperature, the role of a catalyst, and the equilibrium constant Kc and its calculation.
A focused answer to AQA A-Level Chemistry 3.1.6, covering dynamic equilibrium, Le Chatelier's principle, the effects of concentration, pressure, temperature and catalysts, and writing and calculating the equilibrium constant Kc.
Reviewed by: AI editorial process; not yet individually human-reviewed
Have a quick question? Jump to the Q&A page
Jump to a section
What this dot point is asking
AQA wants you to describe dynamic equilibrium, apply Le Chatelier's principle to predict the effect of changing concentration, pressure and temperature (and to explain the role of a catalyst), and to write an expression for , calculate it from equilibrium amounts, and deduce its units.
Dynamic equilibrium
Le Chatelier's principle
- Concentration: adding a reactant shifts equilibrium to the right (towards products) to remove it; removing a product also shifts it right.
- Pressure (gases): increasing pressure shifts equilibrium towards the side with fewer moles of gas. If both sides have equal moles, pressure has no effect.
- Temperature: increasing temperature shifts equilibrium in the endothermic direction; decreasing it shifts towards the exothermic direction.
- Catalyst: speeds up forward and reverse reactions equally, so it has no effect on the position of equilibrium; it only reaches equilibrium faster.
The equilibrium constant Kc
For the reaction :
Only temperature changes . Changing concentration or pressure shifts the position of equilibrium, but the system adjusts until the ratio returns to the same value; a catalyst does not change (it only reaches equilibrium faster). A large (much greater than 1) means the equilibrium lies far to the right and products dominate; a small (much less than 1) means reactants dominate. This links to industrial compromise conditions, such as the Haber process, where a moderate temperature is chosen: a lower temperature would give a higher equilibrium yield of ammonia (the forward reaction is exothermic, so a lower temperature raises ) but the rate would be too slow to be economic, so a compromise of around 450 degrees Celsius is used alongside an iron catalyst and high pressure.
The units of are found by substituting for each concentration term and cancelling. They are not fixed: they depend on the difference between the total powers on the top and bottom of the expression, so they must be worked out for each equilibrium rather than memorised.
Try this
Q1. State the effect of a catalyst on the position of equilibrium. [1 mark]
- Cue. No effect; it only speeds up reaching equilibrium.
Q2. Predict the effect of increasing pressure on . [2 marks]
- Cue. Shifts right (4 moles of gas to 2 moles), increasing the yield of ammonia.
Exam-style practice questions
Practice questions written in the style of AQA exam questions on this dot point, with worked answer explainers. The year tag is the paper they imitate, not the source.
AQA 20183 marksFor an exothermic forward reaction at equilibrium, explain the effect on the position of equilibrium and on of increasing the temperature.Show worked answer →
Increasing the temperature shifts the equilibrium in the endothermic direction to oppose the change. For an exothermic forward reaction, the endothermic direction is the reverse, so the position of equilibrium shifts to the left and the yield of product falls.
Because the equilibrium shifts left, the equilibrium concentrations of products fall and reactants rise, so decreases.
Markers reward the shift in the endothermic direction, the leftward shift, and the decrease in (temperature is the only factor that changes ).
AQA 20224 marksIn the equilibrium , a vessel at equilibrium contains , and . Calculate and state its units.Show worked answer →
Convert amounts to concentrations by dividing by the volume: , , .
.
Units: , so .
Markers reward converting moles to concentrations, the correct expression, the value, and deriving the units.
Related dot points
- Collision theory, the Maxwell-Boltzmann distribution, the effect of temperature, concentration, pressure, surface area and catalysts on rate, and how catalysts lower activation energy.
A focused answer to AQA A-Level Chemistry 3.1.5, covering collision theory, the Maxwell-Boltzmann distribution, the effects of temperature, concentration, pressure and surface area on rate, and how catalysts work.
- Mole fractions and partial pressures, the equilibrium constant Kp written in terms of partial pressures, calculating Kp, and the effect of changing conditions on Kp.
A focused answer to AQA A-Level Chemistry 3.1.10, covering mole fractions and partial pressures, writing and calculating the equilibrium constant Kp for gaseous equilibria, and the effect of changing conditions on Kp.
- Enthalpy change, exothermic and endothermic reactions, standard enthalpy changes (formation, combustion), calorimetry and the equation q = mcDeltaT, Hess's law and enthalpy cycles, mean bond enthalpies.
A focused answer to AQA A-Level Chemistry 3.1.4, covering enthalpy change, exothermic and endothermic reactions, standard enthalpy definitions, calorimetry, Hess's law cycles and mean bond enthalpy calculations.
- Bronsted-Lowry acids and bases, the pH scale and calculating pH of strong acids, the ionic product of water Kw, weak acids and Ka, pH curves and titrations, and buffer action.
A focused answer to AQA A-Level Chemistry 3.1.12, covering Bronsted-Lowry acids and bases, the pH scale, the ionic product of water Kw, weak acids and Ka, pH curves and indicators, and how buffers work.
Sources & how we know this
- AQA A-level Chemistry (7405) specification — AQA (2015)