By Fatskills Exam Guides Team — the exam nerds behind 28,500+ quizzes and 2.1M practice questions across 500+ global exams.
Complete Guide For GCSE/A-Level Chemistry (Edexcel, AQA, OCR)
"Mastering lattice enthalpy and Born-Haber cycles lets you predict whether a compound will form—and it’s worth up to 6 marks in your A-Level exam. Miss this, and you’ll lose easy marks on enthalpy calculations, ionic bonding, and even solubility trends."
Before starting, you must understand:1. Enthalpy changes (ΔH) – Exothermic (–ΔH) vs. endothermic (+ΔH).2. Ionic bonding – How ions form and attract in a lattice.3. Hess’s Law – The total enthalpy change is the same, regardless of the route taken.
MEMORISE THIS – You’ll rearrange it to find ΔHₗₐₜₜ.
Follow these steps for every Born-Haber cycle question:
Write the formation equation (1 mole of compound from elements in standard states). Example: Na(s) + ½Cl₂(g) → NaCl(s)
Draw the Born-Haber cycle as a diagram (or list steps in order):
Form the lattice (Na⁺(g) + Cl⁻(g) → NaCl(s)).
Label each step with its enthalpy change (given in the question or data booklet).
Apply Hess’s Law:
Rearrange to solve for ΔHₗₐₜₜ.
Check signs:
Endothermic steps (+ΔH): Atomisation, ionisation.
Calculate and box your final answer.
Question: Calculate the lattice enthalpy of NaCl using the following data: - ΔH_f° (NaCl) = –411 kJ/mol - ΔH_at (Na) = +108 kJ/mol - ΔH_at (Cl) = +122 kJ/mol - ΔH_IE₁ (Na) = +496 kJ/mol - ΔH_EA₁ (Cl) = –349 kJ/mol
Solution:1. Formation equation: Na(s) + ½Cl₂(g) → NaCl(s) ΔH_f° = –411 kJ/mol
Na⁺(g) + Cl⁻(g) → NaCl(s) ΔHₗₐₜₜ = ?
Apply Hess’s Law: ΔH_f° = ΔH_at (Na) + ΔH_at (Cl) + ΔH_IE₁ (Na) + ΔH_EA₁ (Cl) + ΔHₗₐₜₜ –411 = +108 + +122 + +496 + (–349) + ΔHₗₐₜₜ
Solve for ΔHₗₐₜₜ: –411 = +377 + ΔHₗₐₜₜ ΔHₗₐₜₜ = –411 – 377 = –788 kJ/mol
What we did and why: We used the Born-Haber cycle to break down the formation of NaCl into steps, then rearranged to find the lattice enthalpy. The negative sign confirms it’s exothermic (energy released when ions form a lattice).
Question: Calculate the lattice enthalpy of MgO using: - ΔH_f° (MgO) = –602 kJ/mol - ΔH_at (Mg) = +148 kJ/mol - ΔH_at (O) = +249 kJ/mol - ΔH_IE₁ (Mg) = +738 kJ/mol - ΔH_IE₂ (Mg) = +1451 kJ/mol - ΔH_EA₁ (O) = –141 kJ/mol - ΔH_EA₂ (O) = +798 kJ/mol
Solution:1. Formation equation: Mg(s) + ½O₂(g) → MgO(s) ΔH_f° = –602 kJ/mol
Mg²⁺(g) + O²⁻(g) → MgO(s) ΔHₗₐₜₜ = ?
Apply Hess’s Law: ΔH_f° = ΔH_at (Mg) + ΔH_at (O) + ΔH_IE₁ (Mg) + ΔH_IE₂ (Mg) + ΔH_EA₁ (O) + ΔH_EA₂ (O) + ΔHₗₐₜₜ –602 = +148 + +249 + +738 + +1451 + (–141) + +798 + ΔHₗₐₜₜ
Solve for ΔHₗₐₜₜ: –602 = +3243 + ΔHₗₐₜₜ ΔHₗₐₜₜ = –602 – 3243 = –3845 kJ/mol
What we did and why: MgO has a 2+ ion, so we included two ionisation energies for Mg and two electron affinities for O. The large negative lattice enthalpy shows strong ionic bonding.
Question: Calculate the lattice enthalpy of CaF₂ using: - ΔH_f° (CaF₂) = –1220 kJ/mol - ΔH_at (Ca) = +178 kJ/mol - ΔH_at (F) = +79 kJ/mol - ΔH_IE₁ (Ca) = +590 kJ/mol - ΔH_IE₂ (Ca) = +1145 kJ/mol - ΔH_EA₁ (F) = –328 kJ/mol
Solution:1. Formation equation: Ca(s) + F₂(g) → CaF₂(s) ΔH_f° = –1220 kJ/mol
Ca²⁺(g) + 2F⁻(g) → CaF₂(s) ΔHₗₐₜₜ = ?
Apply Hess’s Law: ΔH_f° = ΔH_at (Ca) + ΔH_at (F) + ΔH_IE₁ (Ca) + ΔH_IE₂ (Ca) + 2 × ΔH_EA₁ (F) + ΔHₗₐₜₜ –1220 = +178 + +158 + +590 + +1145 + (–656) + ΔHₗₐₜₜ
Solve for ΔHₗₐₜₜ: –1220 = +1415 + ΔHₗₐₜₜ ΔHₗₐₜₜ = –1220 – 1415 = –2635 kJ/mol
What we did and why: CaF₂ has two F⁻ ions, so we doubled the atomisation and electron affinity values. The large lattice enthalpy reflects strong ionic bonds in CaF₂.
"Right, listen up—this is your last-minute lifesaver for lattice enthalpy and Born-Haber cycles. Here’s what you must remember:
If you see MgO or CaF₂ in the exam, don’t panic—just remember to include all ionisation steps and double the non-metal values. Now go smash that question!"
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