Verified Solution • 2025–26 Session moderate

QJEEAdv18Ch1e74: JEE Advanced 2018 Chemistry - Class 12 JEEAdv18Ch1e74 Solution: Consider the following reversible reaction, The activation…

Consider the following reversible reaction, A(g)+B(g)→AB(g).A\left( g \right) + B\left( g \right) \to AB\left( g \right).

The activation energy of the backward reaction exceeds that of the forward reaction by 2RT2RT (in J mol−1J\,mo{l^{ - 1}} ). If the pre-exponential factor of the forward reaction is 44 times that of the reverse reaction, the absolute value of ΔG∘\Delta {G^ \circ } (in J mol−1J\,mo{l^{ - 1}} ) for the reaction at 300300 KK is ____________.

(Given; ln⁡(2)=0.7,RT=2500\ln \left( 2 \right) = 0.7,RT = 2500 J mol−1J\,mo{l^{ - 1}} at 300300 KK and GG is the Gibbs energy)

Step-by-Step Verified Solution

At 300 K300 \mathrm{~K} ,

For the reversible reaction,

A(g)+B(g)⇌AB(g)\mathrm{A}(g)+\mathrm{B}(g) \rightleftharpoons \mathrm{AB}(g)

(i) Pre-exponential factor for forward reaction (Af)=4×\left(A_f\right)=4 \times pre-exponential factor for backward reverse reaction (Ab)\left(A_b\right)

Af=4×AbA_f=4 \times A_b

(ii) Activation energy for backward reaction (Eb)f−\left(E_b\right)_f- Activation energy =2RT=2 \mathrm{RT} for forward reaction (Ea)f−\left(\mathrm{E}_a\right)_{f^{-}}

Ab−Af=2RT\mathrm{A}_b-\mathrm{A}_f=2 \mathrm{RT}

amp;(iii) Equilibrium constant (Keq)=Kf Kbamp; Keq=Af×e−(Ea)f/RTAb×e−(Ea)b/RT\begin{aligned}& \text {(iii) Equilibrium constant }\left(\mathrm{K}_{e q}\right)=\frac{\mathrm{K}_f}{\mathrm{~K}_b} \\\\& \mathrm{~K}_{e q}=\frac{\mathrm{A}_f \times e^{-\left(\mathrm{E}_a\right)_f} / \mathrm{RT}}{\mathrm{A}_b \times e^{-\left(\mathrm{E}_a\right)_b} / \mathrm{RT}}\end{aligned}

Keqamp;=Af Ab×e[−(Ea)f−(Ea)b]/RTKeqamp;=4 Ab Ab×e−[2RT/RT]Keqamp;=4×e−2ln⁡Keqamp;=ln⁡4+2ln⁡ln⁡Keqamp;=2ln⁡2+2=2×0.7+2amp;=(1.4+2)=3.4\begin{aligned}\mathrm{K}_{e q} & =\frac{\mathrm{A}_f}{\mathrm{~A}_b} \times e^{\left[-\left(\mathrm{E}_a\right)_f-\left(\mathrm{E}_a\right)_b\right]} / \mathrm{RT} \\\\\mathrm{K}_{e q} & =\frac{4 \mathrm{~A}_b}{\mathrm{~A}_b} \times e^{-[2 \mathrm{RT} / \mathrm{RT}]} \\\\\mathrm{K}_{e q} & =4 \times e^{-2} \\\\\ln \mathrm{K}_{e q} & =\ln 4+2 \ln \\\\\ln \mathrm{K}_{e q} & =2 \ln 2+2=2 \times 0.7+2 \\\\& =(1.4+2)=3.4\end{aligned}

The expression for the change in Gibbs free energy of reaction (ΔG)(\Delta \mathrm{G}) is given as:

ΔG=ΔG∘+RTln⁡k\Delta \mathrm{G}=\Delta \mathrm{G}^{\circ}+\mathrm{RT} \ln k

At equilibrium, ΔG=0\Delta \mathrm{G}=0

ΔG∘=−RTln⁡Keq\Delta \mathrm{G}^{\circ}=-\mathrm{RT} \ln \mathrm{K}_{e q}

Substituting the value of RT and ln⁡Keq\ln \mathrm{K}_{e q}

ΔG∘amp;=−2500 J mol−1×3.4ΔG∘amp;=−8500 J mol−1\begin{aligned}\Delta \mathrm{G}^{\circ} & =-2500 \mathrm{~J} \mathrm{~mol}^{-1} \times 3.4 \\\\\Delta \mathrm{G}^{\circ} & =-8500 \mathrm{~J} \mathrm{~mol}^{-1}\end{aligned}

The absolute value of Gibbs free energy (ΔG∘)\left(\Delta \mathrm{G}^{\circ}\right) for the reaction at 300 K300 \mathrm{~K} is 8500 J mol−18500 \mathrm{~J} \mathrm{~mol}^{-1} .

Related Learning Resources & Exam Preparation