Chemistry
Equilibrium, acids and organic chemistry
- 1.
For N2(g) + 3H2(g) <=> 2NH3(g), the forward reaction is exothermic. Explain how increasing pressure and increasing temperature affect equilibrium yield of ammonia.
[3 marks] · no calculatorAnswer explanation
Draft walkthroughs are based on marking guidance, not independently verified derivations.
- Treat pressure and temperature as separate changes. Compare gas mole counts for pressure and heat direction for temperature.
- Increasing pressure favours the side with fewer gas molecules.
- The product side has 2 moles of gas versus 4, so ammonia yield increases.
- Increasing temperature favours the endothermic reverse reaction, reducing ammonia yield.
Marking points
- Increasing pressure favours the side with fewer gas molecules.
- The product side has 2 moles of gas versus 4, so ammonia yield increases.
- Increasing temperature favours the endothermic reverse reaction, reducing ammonia yield.
Examiner tip: A catalyst changes the rate of reaching equilibrium, not its equilibrium yield.
- 2.
Calculate the pH of 0.020 mol dm^-3 hydrochloric acid, assuming complete dissociation.
[3 marks]Answer explanation
Draft walkthroughs are based on marking guidance, not independently verified derivations.
- For this strong monoprotic acid, complete dissociation makes hydrogen-ion concentration equal to acid concentration.
- HCl dissociates completely, so [H+] = 0.020 mol dm^-3.
- pH = -log10[H+].
- pH = 1.70 to two decimal places.
Marking points
- HCl dissociates completely, so [H+] = 0.020 mol dm^-3.
- pH = -log10[H+].
- pH = 1.70 to two decimal places.
Examiner tip: Use base-ten logarithms for pH, not natural logarithms.
- 3.
Explain why refluxing ethanol with excess acidified potassium dichromate(VI) forms ethanoic acid, while distilling the product early can yield ethanal.
[4 marks] · no calculatorAnswer explanation
Draft walkthroughs are based on marking guidance, not independently verified derivations.
- Follow the oxidation sequence from primary alcohol to aldehyde to carboxylic acid; then ask whether the intermediate stays in contact with oxidant.
- Ethanol is a primary alcohol; its first oxidation product is ethanal.
- Reflux keeps volatile compounds in the reaction mixture.
- Excess oxidant allows ethanal to oxidise further to ethanoic acid.
- Distillation removes ethanal as it forms, limiting further oxidation.
Marking points
- Ethanol is a primary alcohol; its first oxidation product is ethanal.
- Reflux keeps volatile compounds in the reaction mixture.
- Excess oxidant allows ethanal to oxidise further to ethanoic acid.
- Distillation removes ethanal as it forms, limiting further oxidation.
Examiner tip: Reflux retains volatile material; distillation removes it. Conditions determine whether further oxidation occurs.
Marking points are indicative, not an official mark scheme. Accept equivalent valid methods and supported interpretations that address the task; award each mark once without requiring the model wording.