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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.
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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).