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Welcome to GCSE Edexcel Science revision.

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Unit C C 12: Dynamic equilibria.

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A reversible reaction can proceed in both directions: products can react to reform reactants.

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The reversible arrow symbol shows forward and reverse processes.

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Changing conditions can favour one direction.

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Reversibility is chemical reaction in both directions, not just two unrelated processes.

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When ammonium chloride is heated, it can decompose to ammonia and hydrogen chloride gases: N H 4 C L solid reversibly produces N H 3 gas plus H C L gas.

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On cooling, ammonia and hydrogen chloride recombine to form solid ammonium chloride.

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The second gas is hydrogen chloride, not hydrogen.

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The gaseous products are ammonia and hydrogen chloride, not hydrogen.

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The forward and reverse reactions have opposite energy changes: if one is exothermic, the reverse is endothermic.

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Heating can favour the endothermic direction.

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This decomposition is a supervised demonstration using suitable ventilation and safety controls; the gases are not suitable for an unsupervised home experiment.

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A reversible reaction can reach dynamic equilibrium in a closed system, where reactants and products cannot escape.

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At equilibrium the forward and reverse reactions continue at equal rates. “Dynamic” means reactions are still happening at particle level.

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The amounts or concentrations of reactants and products remain constant while conditions remain unchanged.

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They do not have to be equal to each other.

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Starting with reactants only, the forward rate can initially be high while the reverse rate is zero.

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As product forms, the reverse rate rises until both match.

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At equilibrium reactions continue; their rates match rather than becoming zero.

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If products escape from an open system, the reverse reaction may not establish the same equilibrium.

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Closed-system conditions matter.

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The equilibrium position describes how much reactant and product the mixture contains.

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An equilibrium further to the right has a greater proportion of products; further to the left means a greater proportion of reactants.

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A change in conditions disturbs an equilibrium; the system responds in a direction that partly opposes the change until a new equilibrium is reached.

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Increasing a reactant's concentration favours the direction that uses it, often forward.

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Removing a product can favour more product formation; adding product tends to favour the reverse reaction.

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Increasing temperature favours the endothermic direction.

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Decreasing temperature favours the exothermic direction.

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Use the energy change of the stated forward reaction.

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Increasing pressure favours the side with fewer gaseous particles; decreasing pressure favours more gaseous particles.

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Count gaseous coefficients, not atoms or solids.

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Concentration changes favour consuming what was added or replacing what was removed.

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If both sides have equal numbers of gaseous particles, pressure change has no equilibrium-position effect in this model.

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Solid and liquid terms do not count towards the gaseous total.

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A catalyst speeds both forward and reverse reactions and reaches equilibrium sooner.

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It does not change equilibrium position or the equilibrium yield at the same conditions.

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Rate and equilibrium yield are different: conditions giving more product at equilibrium may make the reaction too slow for an economical process.

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The Haber process makes ammonia by the reversible reaction N 2 gas plus 3 H 2 gas reversibly produces 2 N H 3 gas.

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Nitrogen is obtained from air and hydrogen commonly from natural gas.

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The forward reaction is exothermic.

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Four moles of reactant gas correspond to two moles of product gas, so pressure favours the product side.

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Count coefficients of gases, not the total atoms in their molecules.

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The specified industrial conditions are about 450 degrees Celsius, about 200 atmospheres and an iron catalyst.

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These are a practical compromise, not conditions giving the greatest possible equilibrium yield.

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A lower temperature gives a higher equilibrium ammonia yield but a slower rate.

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A moderate high temperature allows useful production speed with a lower equilibrium yield.

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Higher pressure increases equilibrium yield and can increase rate, but compression and strong equipment cost energy and money.

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Very high pressure is not automatically the best economic choice.

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The iron catalyst gives a faster rate without increasing equilibrium yield.

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It lets the process operate efficiently under the chosen conditions.

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Ammonia is cooled so it condenses and can be removed.

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Unreacted nitrogen and hydrogen are recycled through the reactor.

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This uses the starting materials more efficiently, even though only some react each time through.

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Recycling improves overall conversion without requiring complete reaction in one pass.

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For exothermic N 2 plus 3 H 2 reversibly produces 2 N H 3, raising temperature shifts left, raising pressure shifts right, and removing ammonia favours further ammonia formation.

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For an endothermic forward reaction, heating instead shifts right.

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Always identify which written direction is endothermic before making a temperature prediction.

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For H 2 gas plus I 2 gas reversibly produces 2 H I gas, gaseous totals are two on both sides, so a pressure change does not change equilibrium position in this GCSE model.

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On a rate, time graph, equilibrium begins where forward and reverse rates are equal and stay equal.

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On a concentration, time graph, constant values need not have the same height.

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Explain industrial conditions with both chemistry and costs. “High temperature makes more ammonia” is wrong for equilibrium yield even though heating increases rate.

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That completes Dynamic equilibria.

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Revisit the notes and test yourself on the revision website.
