AQA A-LEVEL CHEMISTRY

Topic 3.1.8: Thermodynamics Exam Practice

Test your understanding of lattice enthalpy, Born-Haber cycles, entropy, and Gibbs free energy with exam-style questions.

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Structured Questions

Answer the questions below in the spaces provided. Check your answers with the mark schemes and examiner tips.

Question 1: Born-Haber Cycles & Bonding Character

7 marks

The Born-Haber cycle for sodium chloride contains several steps.

(a) Name the enthalpy changes represented by the following processes:
• (i) Na(s) → Na(g)
• (ii) Cl(g) + e⁻ → Cl⁻(g)
• (iii) Na⁺(g) + Cl⁻(g) → NaCl(s) [3]

(b) Explain why the lattice enthalpy of formation of magnesium oxide (MgO) is significantly more exothermic than that of sodium chloride (NaCl). [4]

Show Mark Scheme

(a)

  • (i) Enthalpy of atomisation of sodium [1]
  • (ii) First electron affinity of chlorine [1]
  • (iii) Lattice enthalpy of formation of sodium chloride [1]

(b)

  • Mg²⁺ and O²⁻ ions have larger charges (+2 and -2 respectively) compared to Na⁺ and Cl⁻ (+1 and -1) [1]
  • Mg²⁺ has a smaller ionic radius than Na⁺ OR O²⁻ has a smaller ionic radius than Cl⁻ [1]
  • There is a much stronger electrostatic attraction between the ions in magnesium oxide [1]
  • More energy is released when the lattice is formed, making the enthalpy of formation significantly more exothermic [1]
Examiner Tip: In questions comparing lattice enthalpies, structure your answer to discuss ionic charge first, then ionic radius, and finally the strength of electrostatic attraction.

Question 2: Dissolution of Magnesium Chloride

8 marks

When magnesium chloride dissolves in water, the temperature of the mixture increases.

(a) Define enthalpy of solution. [2]

(b) Calculate the enthalpy of solution of magnesium chloride (MgCl₂) using the following data:
• Lattice dissociation enthalpy of MgCl₂ = +2526 kJ mol⁻¹
• Hydration enthalpy of Mg²⁺(g) = −1920 kJ mol⁻¹
• Hydration enthalpy of Cl⁻(g) = −378 kJ mol⁻¹ [3]

(c) Explain, in terms of the forces between particles, why the hydration of gaseous ions is an exothermic process. [3]

Show Mark Scheme

(a)

  • The enthalpy change when one mole of an ionic solid [1]
  • is completely dissolved in water to form infinitely dilute aqueous ions under standard conditions [1]

(b)

  • Enthalpy of Solution = Lattice dissociation enthalpy + Hydration enthalpy of Mg²⁺ + 2 × Hydration enthalpy of Cl⁻ [1]
  • Enthalpy of Solution = +2526 + (−1920) + 2 × (−378) [1]
  • Enthalpy of Solution = −150 kJ mol⁻¹ [1]

(c)

  • Water molecules are polar, with oxygen being delta negative and hydrogen being delta positive [1]
  • Electrostatic attractions (ion-dipole forces) form between the gaseous ions and the polar water molecules [1]
  • Forming attractions releases energy, making the process exothermic [1]
Examiner Tip: Be careful to multiply the hydration enthalpy of the chloride ion by 2, as there are two moles of chloride ions in one mole of MgCl₂. Always show your working clearly.

Question 3: Entropy & Gibbs Free Energy

8 marks

The thermal decomposition of calcium carbonate is represented by the equation:
CaCO₃(s) → CaO(s) + CO₂(g)
Standard enthalpies of formation (ΔHf) and standard entropies (\(S\)) are:
• CaCO₃(s): ΔHf = −1207 kJ mol⁻¹, \(S = 93\text{ J K}^{-1}\text{mol}^{-1}\)
• CaO(s): ΔHf = −635 kJ mol⁻¹, \(S = 40\text{ J K}^{-1}\text{mol}^{-1}\)
• CO₂(g): ΔHf = −394 kJ mol⁻¹, \(S = 214\text{ J K}^{-1}\text{mol}^{-1}\)

(a) Calculate the enthalpy change (ΔH) for this reaction. [2]

(b) Calculate the entropy change (ΔS) for this reaction. [2]

(c) Calculate the minimum temperature, in Kelvin, at which this reaction becomes feasible. Show your working. [4]

Show Mark Scheme

(a)

  • \(\Delta H = \Sigma\Delta H_{\text{f}}\text{(products)} - \Sigma\Delta H_{\text{f}}\text{(reactants)}\) [1]
  • ΔH = [(−635) + (−394)] − [−1207] = +178 kJ mol⁻¹ [1]

(b)

  • \(\Delta S = \Sigma S\text{(products)} - \Sigma S\text{(reactants)}\) [1]
  • ΔS = [40 + 214] − 93 = +161 J K⁻¹mol⁻¹ [1]

(c)

  • For a reaction to be feasible, ΔG ≤ 0. Setting ΔG = 0 gives \(T = \frac{\Delta H}{\Delta S}\) [1]
  • Convert ΔH to J mol⁻¹: +178 kJ mol⁻¹ = +178,000 J mol⁻¹ [1]
  • \(T = \frac{178,000}{161}\) [1]
  • \(T =\) 1106 K (or 1105.6 K) [1]
Examiner Tip: A very common error in free energy calculations is neglecting to convert ΔH from kJ to J (or ΔS from J to kJ). Ensure both quantities are in compatible energy units before dividing.