Step 1: Calculate $\Delta G^\circ_{reaction$.}
Reaction: \(A_2 \rightleftharpoons 2A\)
\[ \Delta G^\circ_{rxn} = 2\Delta G^\circ(A) - \Delta G^\circ(A_2) \]
\[ \Delta G^\circ_{rxn} = 2(-50.8625) - (-100) = -101.725 + 100 = -1.725\,\text{kJ/mol} = -1725\,\text{J/mol} \]
Step 2: Calculate Equilibrium Constant K.
\[ \Delta G^\circ = -RT \ln K \]
\[ -1725 = -(8.3)(300) \ln K \]
\[ \ln K = \frac{1725}{2490} \approx 0.693 \]
\[ K \approx e^{0.693} \approx 2 \]
Step 3: Relate K to degree of dissociation $\alpha$.
For \(A_2 \rightleftharpoons 2A\) starting with 1 mole at 1 atm pressure:
Total moles at equilibrium = \(1 - \alpha + 2\alpha = 1 + \alpha\).
Partial pressures: \(p_{A2} = \frac{1-\alpha}{1+\alpha}P\), \(p_A = \frac{2\alpha}{1+\alpha}P\).
\[ K_p = \frac{(p_A)^2}{p_{A2}} = \frac{4\alpha^2 P}{(1-\alpha)(1+\alpha)} = \frac{4\alpha^2}{1-\alpha^2} \]
Since K = 2:
\[ 2 = \frac{4\alpha^2}{1-\alpha^2} \implies 1-\alpha^2 = 2\alpha^2 \implies 3\alpha^2 = 1 \]
\[ \alpha = \frac{1}{\sqrt{3}} \approx 0.577 \]
Step 4: Format the answer.
\(\alpha = 57.7 \times 10^{-2}\).
Rounding to nearest integer implies x = 58.