Calculate ΔG° for reaction with ΔH°=-92kJ and ΔS°=-198 J/K at 298K — is it spontaneous

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Question

For a reaction, ΔH°=92\Delta H° = -92 kJ/mol and ΔS°=198\Delta S° = -198 J/K/mol at 298 K. Calculate ΔG°\Delta G° and predict whether the reaction is spontaneous at this temperature.

Solution — Step by Step

The Gibbs-Helmholtz equation relates ΔG\Delta G, ΔH\Delta H, and ΔS\Delta S:

ΔG°=ΔH°TΔS°\Delta G° = \Delta H° - T \Delta S°

This equation tells us that spontaneity depends on the balance between enthalpy (energy released) and entropy (disorder change) at a given temperature.

ΔH°=92\Delta H° = -92 kJ/mol = 92,000-92{,}000 J/mol

ΔS°=198\Delta S° = -198 J/K/mol (already in J, not kJ)

T=298T = 298 K

We must convert ΔH°\Delta H° to J (or ΔS°\Delta S° to kJ) before substituting — mixing kJ and J is the most common mistake in this type of problem.

TΔS°=298×(198)=59,004 J/mol=59.004 kJ/molT \Delta S° = 298 \times (-198) = -59{,}004 \text{ J/mol} = -59.004 \text{ kJ/mol} ΔG°=ΔH°TΔS°=92,000(59,004)\Delta G° = \Delta H° - T\Delta S° = -92{,}000 - (-59{,}004) ΔG°=92,000+59,004=32,996 J/mol\Delta G° = -92{,}000 + 59{,}004 = -32{,}996 \text{ J/mol} ΔG°33 kJ/mol\Delta G° \approx -33 \text{ kJ/mol}

Since ΔG°<0\Delta G° < 0 (negative), the reaction is spontaneous at 298 K under standard conditions.

Why This Works

The sign of ΔG°\Delta G° tells us the direction of spontaneous change at constant temperature and pressure:

  • ΔG°<0\Delta G° < 0: spontaneous (forward reaction favoured)
  • ΔG°>0\Delta G° > 0: non-spontaneous (reverse reaction favoured)
  • ΔG°=0\Delta G° = 0: system at equilibrium

In this problem, both ΔH°\Delta H° (negative = exothermic, favours spontaneity) and ΔS°\Delta S° (negative = decrease in disorder, opposes spontaneity) work against each other. The enthalpy effect wins at 298 K, making ΔG°\Delta G° negative.

At higher temperatures, the TΔS°T|\Delta S°| term grows larger, and eventually ΔG°\Delta G° will become positive — the reaction becomes non-spontaneous above a crossover temperature T=ΔH°/ΔS°T^* = \Delta H° / \Delta S°.

T=92,000198465 KT^* = \frac{-92{,}000}{-198} \approx 465 \text{ K}

Above 465 K, this reaction is non-spontaneous.

Alternative Method — Finding Crossover Temperature

If asked “at what temperature does the reaction stop being spontaneous?”:

Set ΔG°=0\Delta G° = 0:

0=ΔH°TΔS°T=ΔH°ΔS°=92000198465 K0 = \Delta H° - T \Delta S° \Rightarrow T = \frac{\Delta H°}{\Delta S°} = \frac{-92000}{-198} \approx 465 \text{ K}

The reaction is spontaneous for T<465T < 465 K.

Common Mistake

Unit mismatch is the #1 error here. Students write ΔG°=92298×(198)=92+58,904\Delta G° = -92 - 298 \times (-198) = -92 + 58,904, forgetting to convert ΔH°\Delta H° from kJ to J. They get +58,812+58,812 kJ — wildly wrong. Always check: if ΔH°\Delta H° is in kJ, convert ΔS°\Delta S° to kJ/K (divide by 1000), or convert ΔH°\Delta H° to J (multiply by 1000). Never mix units.

In JEE Main, this type of problem often adds “find the temperature at which equilibrium is attained” — that means find TT where ΔG°=0\Delta G° = 0, i.e., T=ΔH°/ΔS°T = \Delta H° / \Delta S°. This appeared in JEE Main 2022 Session 2.

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