Concept:
The spontaneity and direction of a chemical reaction are determined using Gibbs free energy and the relation between reaction quotient $(Q)$ and equilibrium constant $(K)$:
\[
\Delta G = \Delta G^\circ + RT \ln Q
\]
Also,
\[
\Delta G^\circ = -RT \ln K
\]
From these relations:
• If $Q < K$, then $\Delta G < 0$ → reaction proceeds in forward direction
• If $Q > K$, then $\Delta G > 0$ → reaction proceeds in reverse direction
• If $Q = K$, system is at equilibrium
Step 1: Write expression for reaction quotient $Q$.
For the reaction:
\[
\frac{3}{2}A \rightarrow B
\]
\[
Q = \frac{[B]}{[A]^{3/2}}
\]
Substitute given values:
\[
Q = \frac{1}{(10000)^{3/2}}
\]
Step 2: Simplify $Q$.
\[
10000 = 10^4 \Rightarrow (10^4)^{3/2} = 10^{6}
\]
\[
Q = \frac{1}{10^6} = 10^{-6}
\]
Step 3: Determine equilibrium constant $K$ using $\Delta G^\circ$.
\[
\Delta G^\circ = -RT \ln K
\]
Given $\Delta G^\circ = +163\ \text{kJ mol}^{-1}$ (positive), therefore:
\[
\ln K < 0 \Rightarrow K < 1
\]
Thus, equilibrium strongly favors reactants and $K$ is very small.
Step 4: Compare $Q$ and $K$.
We found:
\[
Q = 10^{-6}
\]
Since $K$ is much smaller than 1 (due to large positive $\Delta G^\circ$), we get:
\[
Q > K
\]
Step 5: Determine direction of reaction.
Since:
\[
Q > K \Rightarrow \Delta G > 0
\]
The reaction will proceed in the reverse direction to attain equilibrium.