The rate constants $k_1$ and $k_2$ for two different reactions are $10^{16} \cdot e^{-2000/T}$ and $10^{15} \cdot e^{-1000/T},$ respectively. The temperature at which $k_1 = k_2$ is

Decomposition of a hydrocarbon follows the equation $k = (5.5 \times 10^{11} \text{ s}^{-1}) e^{\frac{-28000 \text{ K}}{T}}$. The activation energy of the reaction is . . . . . . $\text{kJ mol}^{-1}$. (Nearest Integer) Given: $R = 8.3 \text{ J K}^{-1} \text{ mol}^{-1}$

The specific rate constant of a first-order reaction depends on .......

For the reaction,$A \rightleftharpoons B$,$E_a = 50 \ kJ \ mol^{-1}$ and $\Delta H = -20 \ kJ \ mol^{-1}$. When a catalyst is added,$E_a$ decreases by $10 \ kJ \ mol^{-1}$. What is the $E_a$ for the backward reaction in the presence of the catalyst?

For a hypothetical reaction $A \to B$,the activation energies for forward and backward reactions are $19 \ kJ/mol$ and $9 \ kJ/mol$ respectively. The heat of reaction is $.... \ kJ$.

For an elementary chemical reaction, the Arrhenius plot is given below. If the energy of activation is $6.64 \ kJ \ mol^{-1}$ and $R = 8.3 \ J \ K^{-1} \ mol^{-1}$, the temperature at which the rate constant becomes $e^2 \ min^{-1}$, is (in $K$)