Skip to content
Marlbridge

Flashcards · 9701 · A Level Topic 23

Chemical energetics (A Level) flashcards

21 cards on A Level Topic 23, subtopics 23.1 to 23.4. Pick a subtopic or study them all.

Study mode needs JavaScript. Every card is listed below, so you can still cover the answers and test yourself.

All 21 cards

For a quick read-through or printing. Cover the right-hand side to test yourself.

23.1 Lattice energy and Born-Haber cycles

Lattice energy, ΔHlatt
The enthalpy change when one mole of an ionic compound is formed from its gaseous ions under standard conditions. Always exothermic (negative).
Enthalpy change of atomisation
The enthalpy change when one mole of gaseous atoms is formed from the element in its standard state.
First electron affinity
The enthalpy change when one mole of gaseous atoms each gain an electron to form one mole of gaseous 1− ions.
Why is the second electron affinity endothermic?
The electron is being added to an already negative ion, so energy is needed to overcome the repulsion.
Two factors that make a lattice energy more exothermic
Higher ionic charges (this dominates) and smaller ionic radii: lattice energy is proportional to (charge⁺ × charge⁻) ÷ (r⁺ + r⁻). MgO is far more exothermic than NaCl.
Born–Haber cycle: the Hess equation for ΔHf of an ionic solid
ΔHf = Σ(atomisation) + Σ(ionisation energies) + Σ(electron affinities) + ΔHlatt. Watch multipliers: Cl₂ → 2Cl needs 2 × atomisation; Mg²⁺ needs the first and second IE.

23.2 Enthalpies of solution and hydration

Enthalpy change of hydration
The enthalpy change when one mole of gaseous ions dissolves in an excess of water. Always exothermic.
Enthalpy change of solution
The enthalpy change when one mole of solute dissolves in a solvent to form an infinitely dilute solution. It can be positive or negative.
Equation linking ΔHsol, lattice energy and hydration enthalpies
ΔHsol = −ΔHlatt + ΔHhyd(cation) + ΔHhyd(anion)
ΔHlatt(NaCl) = −787, ΔHhyd(Na⁺) = −406, ΔHhyd(Cl⁻) = −364 kJ mol⁻¹. Calculate ΔHsol.
ΔHsol = −(−787) + (−406) + (−364) = 787 − 770 = +17 kJ mol⁻¹
How do ionic charge and radius affect hydration enthalpy?
Higher charge and smaller radius make it more exothermic: stronger attraction between the ion and the polar water molecules.

23.3 Entropy change

Entropy, S
A measure of the dispersal of energy and particles: the number of possible arrangements (disorder) of a system. Units J K⁻¹ mol⁻¹.
Order of entropy for the three states
Gas ≫ liquid > solid.
How do you predict the sign of ΔS for a reaction?
More moles of gas produced: positive. Fewer moles of gas: negative. Melting, boiling and usually dissolving a solid: positive.
How do you calculate ΔS from standard entropies?
ΔS⦵ = ΣS⦵(products) − ΣS⦵(reactants), multiplying each by its coefficient. The answer is in J K⁻¹ mol⁻¹.
Effect of raising temperature on the entropy of a substance
Entropy increases: the particles have more energy and more ways of arranging it.

23.4 Gibbs free energy change

Gibbs equation and the condition for feasibility
ΔG = ΔH − TΔS (T in K; convert ΔS to kJ K⁻¹ mol⁻¹). A reaction is feasible when ΔG is negative (or zero).
Feasibility for each combination of signs of ΔH and ΔS
ΔH −, ΔS +: always feasible. ΔH +, ΔS −: never. ΔH −, ΔS −: at low temperature. ΔH +, ΔS +: at high temperature.
Temperature at which a reaction becomes feasible
Set ΔG = 0: T = ΔH ÷ ΔS (with ΔS in kJ K⁻¹ mol⁻¹ if ΔH is in kJ mol⁻¹).
A reaction has a large negative ΔG but nothing is observed. Why?
Feasible does not mean fast: the activation energy may be so high that the rate is negligible.
ΔH = +178 kJ mol⁻¹, ΔS = +0.161 kJ K⁻¹ mol⁻¹. Minimum temperature for feasibility?
T = ΔH ÷ ΔS = 178 ÷ 0.161 ≈ 1106 K (about 1110 K).