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What makes a reaction feasible, and how do we build Born-Haber cycles?

Lattice enthalpy and Born-Haber cycles, enthalpies of solution and hydration, entropy and the second law, and the use of free energy change to decide the feasibility of a reaction.

A CCEA A-Level Chemistry answer on thermodynamics, covering lattice enthalpy and Born-Haber cycles, enthalpies of solution and hydration, entropy and the second law, and using the free energy change to decide whether a reaction is feasible.

Generated by Claude Opus 4.813 min answer

Reviewed by: AI editorial process; not yet individually human-reviewed

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  1. What this dot point is asking
  2. Lattice enthalpy and Born-Haber cycles
  3. Enthalpies of solution and hydration
  4. Entropy and free energy
  5. Examples in context
  6. Try this

What this dot point is asking

CCEA wants you to define lattice enthalpy, construct Born-Haber cycles, link enthalpies of solution and hydration, define entropy and the second law, and use ΔG=ΔHTΔS\Delta G = \Delta H - T\Delta S to judge feasibility.

Lattice enthalpy and Born-Haber cycles

Enthalpies of solution and hydration

Smaller, more highly charged ions have more exothermic hydration enthalpies because of stronger ion-dipole attraction to water.

Entropy and free energy

Examples in context

Whether a salt dissolves and whether the process feels hot or cold both come from this analysis: ammonium nitrate dissolving is endothermic (ΔHsol>0\Delta H_{sol} > 0) because the lattice energy needed slightly exceeds the hydration energy released, which is why instant cold packs use it. The feasibility test explains why the thermal decomposition of calcium carbonate, endothermic with a positive ΔS\Delta S (a gas is released), only becomes feasible at high temperature once TΔST\Delta S outweighs ΔH\Delta H.

Try this

Q1. Define the lattice enthalpy of formation. [1 mark]

  • Cue. The enthalpy change when one mole of ionic solid forms from its gaseous ions.

Q2. Write the equation linking enthalpy of solution, lattice enthalpy of dissociation and hydration enthalpies. [1 mark]

  • Cue. ΔHsol=ΔHlatt,diss+ΔHhyd\Delta H_{sol} = \Delta H_{latt,diss} + \sum \Delta H_{hyd}.

Q3. A reaction has ΔH=50 kJ mol1\Delta H = -50\ \text{kJ mol}^{-1} and ΔS=100 J K1mol1\Delta S = -100\ \text{J K}^{-1}\,\text{mol}^{-1}. Calculate ΔG\Delta G at 298 K298\ \text{K} and state if it is feasible. [2 marks]

  • Cue. ΔG=50(298×0.100)=50+29.8=20.2 kJ mol1\Delta G = -50 - (298 \times -0.100) = -50 + 29.8 = -20.2\ \text{kJ mol}^{-1}; feasible.

Exam-style practice questions

Practice questions written in the style of CCEA exam questions on this dot point, with worked answer explainers. The year tag is the paper they imitate, not the source.

CCEA 20205 marksUse the following data to calculate the lattice enthalpy of sodium chloride by a Born-Haber cycle: enthalpy of formation 411-411; atomisation of Na\text{Na} +107+107; first ionisation energy of Na\text{Na} +496+496; atomisation of Cl\text{Cl} +122+122; first electron affinity of Cl\text{Cl} 349 kJ mol1-349\ \text{kJ mol}^{-1}.
Show worked answer →

Apply Hess law around the Born-Haber cycle. The enthalpy of formation equals the sum of the steps to gaseous ions plus the lattice enthalpy (formation of the lattice from gaseous ions):

ΔHf=ΔHat(Na)+IE1(Na)+ΔHat(Cl)+EA1(Cl)+ΔHlatt\Delta H_f = \Delta H_{at}(\text{Na}) + IE_1(\text{Na}) + \Delta H_{at}(\text{Cl}) + EA_1(\text{Cl}) + \Delta H_{latt}

Substitute the numbers (all in kJ mol1\text{kJ mol}^{-1}):

411=(+107)+(+496)+(+122)+(349)+ΔHlatt-411 = (+107) + (+496) + (+122) + (-349) + \Delta H_{latt}

411=+376+ΔHlatt-411 = +376 + \Delta H_{latt}

ΔHlatt=411376=787 kJ mol1\Delta H_{latt} = -411 - 376 = -787\ \text{kJ mol}^{-1}

Markers reward (1) the correct Hess-law construction, (2) using the right signs (ionisation positive, electron affinity negative), (3) the arithmetic, (4) the negative value, (5) units kJ mol1\text{kJ mol}^{-1}.

CCEA 20224 marksA reaction has ΔH=+25.0 kJ mol1\Delta H = +25.0\ \text{kJ mol}^{-1} and ΔS=+120 J K1mol1\Delta S = +120\ \text{J K}^{-1}\,\text{mol}^{-1}. Determine whether it is feasible at 298 K298\ \text{K} and find the temperature above which it becomes feasible.
Show worked answer →

Feasibility depends on the free energy change, ΔG=ΔHTΔS\Delta G = \Delta H - T\Delta S, which must be negative (or zero) for a feasible reaction.

Convert ΔS\Delta S to kJ\text{kJ}: 120 J K1mol1=0.120 kJ K1mol1120\ \text{J K}^{-1}\,\text{mol}^{-1} = 0.120\ \text{kJ K}^{-1}\,\text{mol}^{-1}.

At 298 K298\ \text{K}: ΔG=25.0(298×0.120)=25.035.8=10.8 kJ mol1\Delta G = 25.0 - (298 \times 0.120) = 25.0 - 35.8 = -10.8\ \text{kJ mol}^{-1}. Since ΔG\Delta G is negative, the reaction is feasible at 298 K298\ \text{K}.

Feasibility limit when ΔG=0\Delta G = 0: T=ΔHΔS=25.00.120=208 KT = \dfrac{\Delta H}{\Delta S} = \dfrac{25.0}{0.120} = 208\ \text{K}.

Markers reward (1) the ΔG=ΔHTΔS\Delta G = \Delta H - T\Delta S equation, (2) converting ΔS\Delta S units, (3) the value of ΔG\Delta G and the feasible conclusion, (4) the threshold temperature 208 K208\ \text{K}.

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