Step 1: Write the integrated rate equation for a first-order reaction.
For a first-order reaction, the integrated rate law is:
\[
\ln \left( \frac{[A_0]}{[A]} \right) = k \cdot t
\]
where:
- \( [A_0] \) is the initial concentration of A,
- \( [A] \) is the concentration of A at time \( t \),
- \( k \) is the rate constant,
- \( t \) is the time.
Step 2: Use the relationship with pressure.
For gaseous reactions, we can substitute pressure for concentration. The pressure of A at time \( t \) is related to the initial pressure by:
\[
\ln \left( \frac{P_0}{P_t} \right) = k \cdot t
\]
where:
- \( P_0 \) is the initial pressure of A,
- \( P_t \) is the pressure of A at time \( t \),
- \( k \) is the rate constant.
Step 3: Set up the problem.
We are given:
- Initial pressure \( P_0 = 1 \, \text{bar} \),
- Total pressure at time \( t = 100 \, \text{s} \) is 1.5 bar, which is the sum of the pressures of A, B, and C. Since one mole of A produces one mole each of B and C, the pressure of B and C will both be \( P_0 - P_t \). Thus, the total pressure at time \( t \) is \( P_0 + (P_0 - P_t) = 1 + (1 - P_t) \).
So,
\[
P_t = 1 \, \text{bar} - 0.5 \, \text{bar} = 0.5 \, \text{bar}
\]
Thus, the equation becomes:
\[
\ln \left( \frac{1}{0.5} \right) = k \cdot 100
\]
\[
\ln(2) = k \cdot 100
\]
\[
k = \frac{\ln(2)}{100} = \frac{0.693}{100} = 6.93 \times 10^{-3} \, \text{s}^{-1}
\]
Thus, the rate constant \( k \) is \( 6.93 \times 10^{-3} \, \text{s}^{-1} \).