MCQEasyJEE 2025Arrhenius Equation & Activation Energy

JEE Chemistry 2025 Question with Solution

For A2+B22AB\mathrm{A}_{2}+\mathrm{B}_{2} \rightleftharpoons 2\mathrm{AB} Ea\mathrm{E}_{\mathrm{a}} for forward and backward reaction are 180kJ mol1180 \, \text{kJ mol}^{-1} and 200kJ mol1200 \, \text{kJ mol}^{-1} respectively. If catalyst lowers Ea\mathrm{E}_{\mathrm{a}} for both reaction by 100kJ mol1100 \, \text{kJ mol}^{-1}. Which of the following statement is correct?

  • A

    Catalyst does not alter the Gibbs energy change of a reaction.

  • B

    Catalyst can cause non-spontaneous reactions to occur.

  • C

    The enthalpy change for the reaction is +20kJ mol1+20 \, \text{kJ mol}^{-1}.

  • D

    The enthalpy change for the catalysed reaction is different from that of uncatalysed reaction.

Answer

Correct answer:A

Step-by-step solution

Standard Method

Given: A2+B22AB\mathrm{A}_{2}+\mathrm{B}_{2} \rightleftharpoons 2\mathrm{AB}, activation energy for the forward reaction is 180kJ mol1180 \, \text{kJ mol}^{-1} and for the backward reaction is 200kJ mol1200 \, \text{kJ mol}^{-1}. The catalyst lowers both activation energies by 100kJ mol1100 \, \text{kJ mol}^{-1}.

Find: Which statement is correct.

For a reaction profile,

ΔH=Ea,forwardEa,backward\Delta H = E_{a,\text{forward}} - E_{a,\text{backward}}

So,

ΔH=180200=20kJ mol1\Delta H = 180 - 200 = -20 \, \text{kJ mol}^{-1}

Thus, the reaction enthalpy is 20kJ mol1-20 \, \text{kJ mol}^{-1}, not +20kJ mol1+20 \, \text{kJ mol}^{-1}.

A catalyst lowers the activation energy of both forward and backward reactions by the same amount, but it does not change thermodynamic state functions such as ΔH\Delta H or ΔG\Delta G. Therefore, it cannot make a non-spontaneous reaction spontaneous.

So:

  1. Option A is correct because catalyst does not alter Gibbs energy change.
  2. Option B is incorrect because spontaneity depends on ΔG\Delta G, which remains unchanged.
  3. Option C is incorrect because ΔH=20kJ mol1\Delta H = -20 \, \text{kJ mol}^{-1}.
  4. Option D is incorrect because catalysis does not change enthalpy change.

Therefore, the correct option is A.

Using activation energy difference

Given: Forward activation energy =180kJ mol1= 180 \, \text{kJ mol}^{-1}, backward activation energy =200kJ mol1= 200 \, \text{kJ mol}^{-1}.

Find: The correct statement about the effect of catalyst.

First compute the enthalpy change:

ΔH=EfEb\Delta H = E_f - E_b ΔH=180200=20kJ mol1\Delta H = 180 - 200 = -20 \, \text{kJ mol}^{-1}

Now after adding catalyst:

Ef=180100=80kJ mol1E_f' = 180 - 100 = 80 \, \text{kJ mol}^{-1} Eb=200100=100kJ mol1E_b' = 200 - 100 = 100 \, \text{kJ mol}^{-1}

Then,

ΔH=EfEb=80100=20kJ mol1\Delta H' = E_f' - E_b' = 80 - 100 = -20 \, \text{kJ mol}^{-1}

So the enthalpy change remains unchanged even after catalysis.

Also, catalyst changes only the rate by providing an alternative pathway of lower activation energy. It does not change ΔG\Delta G, so it does not change spontaneity.

Therefore, the correct option is A.

Common mistakes

  • Students often think a catalyst changes ΔG\Delta G and hence spontaneity. This is wrong because a catalyst affects only the reaction pathway and activation energy. Use thermodynamic criteria separately from kinetic effects.

  • A common mistake is taking ΔH=Ea,backwardEa,forward\Delta H = E_{a,\text{backward}} - E_{a,\text{forward}} and getting +20kJ mol1+20 \, \text{kJ mol}^{-1}. The correct relation here is ΔH=Ea,forwardEa,backward\Delta H = E_{a,\text{forward}} - E_{a,\text{backward}}.

  • Some students assume lowering both activation energies changes the enthalpy of reaction. This is incorrect because enthalpy depends on initial and final states, not on the path. Keep state functions and path-dependent quantities distinct.

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