Consider a **first-order gas-phase decomposition reaction**: \[ A(g) \rightarrow B(g) + C(g) \]
Let the initial pressure of \( A \) be \( P_i \) and the pressure at time \( t \) be \( P \).
As the reaction proceeds, suppose the partial pressure of \( A \) that decomposes is \( x \).
Then, - Pressure of \( A \) left = \( P_i - x \) - Pressure of \( B \) formed = \( x \) - Pressure of \( C \) formed = \( x \)
Therefore, the total pressure at time \( t \) is: \[ P = (P_i - x) + x + x = P_i + x \] which gives \[ x = P - P_i \]
Hence, the pressure of \( A \) remaining is: \[ P_A = P_i - x = 2P_i - P \]
For a first-order reaction, the integrated rate law is: \[ k = \frac{2.303}{t} \log \frac{P_i}{P_A} \]
Substituting \( P_A = 2P_i - P \): \[ k = \frac{2.303}{t} \log \frac{P_i}{2P_i - P} \]
Therefore, the correct integrated rate law for a first-order gas-phase reaction is: \[ \boxed{k = \frac{2.303}{t} \log \frac{P_i}{2P_i - P}} \]
Rate law for a reaction between $A$ and $B$ is given by $\mathrm{R}=\mathrm{k}[\mathrm{A}]^{\mathrm{n}}[\mathrm{B}]^{\mathrm{m}}$. If concentration of A is doubled and concentration of B is halved from their initial value, the ratio of new rate of reaction to the initial rate of reaction $\left(\frac{\mathrm{r}_{2}}{\mathrm{r}_{1}}\right)$ is
For $\mathrm{A}_{2}+\mathrm{B}_{2} \rightleftharpoons 2 \mathrm{AB}$ $\mathrm{E}_{\mathrm{a}}$ for forward and backward reaction are 180 and $200 \mathrm{~kJ} \mathrm{~mol}^{-1}$ respectively. If catalyst lowers $\mathrm{E}_{\mathrm{a}}$ for both reaction by $100 \mathrm{~kJ} \mathrm{~mol}^{-1}$. Which of the following statement is correct?