ThermodynamicsLattice, hydration & solution

Year 13 · AQA & OCR A

Lattice, hydration & solution enthalpy

Practise lattice enthalpy, hydration enthalpy and enthalpy of solution with calculations, rearrangements and ionic-trend questions.

Calculate, rearrange or explain the trend

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Skill: ionic energeticsIonic energetics · SITE 2.84.0

Draw the solution cycle before rearranging it

I’d draw one mole of solid, the gaseous ions and the aqueous ions before putting any values in. The direct solid-to-aqueous route is ΔHsol.

Use ionic charge and ionic radius

Lattice and hydration trends depend on ionic charge and ionic radius. For example, compare the radii of F and I when explaining their ionic enthalpy trends.

Greater charge strengthens attraction

Larger ionic charges strengthen electrostatic attraction in a lattice and ion–dipole attraction during hydration. That usually makes the corresponding enthalpy more exothermic.

Smaller ions strengthen attraction

For ions with the same charge, a smaller ionic radius lets opposite charges approach more closely. Hydration also becomes more exothermic because water can interact more strongly with the concentrated ionic charge.

Count every hydrated ion

One mole of MgCl2 gives one Mg2+ and two Cl ions. The chloride hydration enthalpy therefore appears twice in the solution cycle.

AQA: compare with the perfect ionic model

Use the size of the discrepancy, then interpret it in the right direction. A Born–Haber value comes from experimental thermochemical data. A perfect ionic model assumes completely ionic bonding. Close agreement supports that model; a substantial discrepancy points to extra covalent character in the real bonding.

Use Born–Haber if the lattice step is the weak point

Practise Born–Haber next if the lattice term is where you get stuck. The full A-level bonding lab also has a shorter conceptual ionic-energetics route alongside complex ions and delocalisation.