Consider $\mathrm{A} \xrightarrow{\mathrm{k}_1} \mathrm{~B}$ and $\mathrm{C} \xrightarrow{\mathrm{k}_2} \mathrm{D}$ are two reactions. If the rate constant $\left(\mathrm{k}_1\right)$ of the $\mathrm{A} \longrightarrow \mathrm{B}$ reaction can be expressed by the following equation $\log _{10} \mathrm{k}=14.34-\frac{1.5 \times 10^4}{\mathrm{~T} / \mathrm{K}}$ and activation energy of $C \longrightarrow D$ reaction $\left(E a_2\right)$ is $\frac{1}{5}$ th of the $A \longrightarrow B$ reaction $\left(E a_1\right)$, then the value of $\left(E a_2\right)$ is
$\_\_\_\_$ $\mathrm{kJ} \mathrm{mol}^{-1}$. (Nearest Integer)
The temperature at which the rate constants of the given below two gaseous reactions become equal is $\_\_\_\_$ K. (Nearest integer)
$$ \begin{array}{ll} \mathrm{X} \longrightarrow \mathrm{Y}, & \mathrm{k}_1=10^6 e^{\frac{-30000}{\mathrm{~T}}} \\ \mathrm{P} \longrightarrow \mathrm{Q}, & \mathrm{k}_2=10^4 e^{\frac{-24000}{\mathrm{~T}}} \end{array} $$
Given : $\ln 10=2.303$
Pre-exponential factors of two different reactions of same order are identical. Let activation energy of first reaction exceeds the activation energy of second reaction by $20 \mathrm{~kJ} \mathrm{~mol}^{-1}$. If $\mathrm{k}_1$ and $\mathrm{k}_2$ are the rate constants of first and second reaction respectively at 300 K , then $\ln \frac{\mathrm{k}_2}{\mathrm{k}_1}$ will be $\_\_\_\_$ . (nearest integer) $\left[\mathrm{R}=8.3 \mathrm{~J} \mathrm{~K}^{-1} \mathrm{~mol}^{-1}\right]$
For the reaction $\mathrm{A} \rightarrow \mathrm{B}$ the following graph was obtained. The time required (in seconds) for the concentration of A to reduce to $2.5 \mathrm{~g} \mathrm{~L}^{-1}$ (if the initial concentration of A was $50 \mathrm{~g} \mathrm{~L}^{-1}$ ) is $\qquad$ . (Nearest integer)
Given : $\log 2=0.3010$

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