Step 1: The Arrhenius equation.
The Arrhenius equation relates the rate constant \( k \) to temperature \( T \) and the activation energy \( E_a \):
\[
k = A e^{\frac{-E_a}{RT}}
\]
Taking the natural logarithm of both sides, we get:
\[
\ln k = \ln A - \frac{E_a}{RT}
\]
This is a linear equation of the form \( y = mx + b \), where the slope \( m \) is \( -\frac{E_a}{R} \). Thus, the activation energy can be found from the slope of the line.
Step 2: Using the slope to find activation energy.
The slope \( m = -\frac{E_a}{R} \), where \( R \) is the universal gas constant (\( R = 8.314 \, \text{J/mol·K} \)). The given slope is \( -2.55 \times 10^4 \, \text{K} \).
We can solve for \( E_a \) as follows:
\[
E_a = -mR = 2.55 \times 10^4 \times 8.314 = 2.12 \times 10^5 \, \text{J/mol}
\]
Step 3: Conclusion.
Thus, the activation energy is \( 2.12 \times 10^5 \, \text{J/mol} \), which corresponds to option (1).
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?