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📋 Key Definitions and Core Concepts
Lattice Enthalpy: Enthalpy change when one mole of solid ionic lattice forms from gaseous ions under standard conditions (exothermic).
Gibbs Free Energy: ΔG = ΔH - TΔS. A reaction is thermodynamically feasible when ΔG ≤ 0.
🔍 Key Principles & Specification Requirements
- Born-Haber: ΔH_f = ΔH_at(metal) + IE(metal) + ΔH_at(non-metal) + EA(non-metal) + ΔH_latt.
- Discrepancy between theoretical (ionic model) and experimental Born-Haber lattice enthalpies indicates covalent character due to polarization.
- ΔG ≤ 0 temperature threshold: T = ΔH / ΔS (ensure units match: J/mol vs kJ/mol).
💡 Worked Example Question
Exam-Style Question
Question:
For CaCO₃(s) → CaO(s) + CO₂(g), ΔH = +178 kJ/mol, ΔS = +161 J/(K·mol). Calculate the temperature above which decomposition is feasible.
Model Solution & Mark Scheme:
Feasible when ΔG ≤ 0 => T ≥ ΔH / ΔS.
ΔH = 178,000 J/mol.
T = 178,000 / 161 = 1105.6 K (833°C).
❓ Practice Questions & Mark Schemes
Q1: Why is lattice enthalpy of MgO much more exothermic than NaCl?
Show Model Answer
Answer: Mg²⁺ and O²⁻ have higher charges (+2/-2 vs +1/-1) and smaller ionic radii, generating much stronger electrostatic forces.
Q2: Explain why dissolving ammonium nitrate in water is endothermic yet spontaneous.
Show Model Answer
Answer: ΔH > 0 but solid-to-aqueous dissolution greatly increases entropy (ΔS >> 0). At 298 K, TΔS > ΔH, making ΔG = ΔH - TΔS < 0.
📄 Past Papers & Exam Resources
🔗 Further Reading & Resources