We use the Arrhenius equation to calculate activation energy: \[ k = A e^{-\frac{E_a}{RT}} \] Where \(k\) is the rate constant, \(A\) is the pre-exponential factor, \(E_a\) is the activation energy, \(R\) is the gas constant (8.314 J/mol·K), and \(T\) is the temperature in Kelvin. The rate doubles, so: \[ \frac{k_2}{k_1} = 2 \] Using the logarithmic form of the Arrhenius equation: \[ \ln\left(\frac{k_2}{k_1}\right) = \frac{E_a}{R} \left( \frac{1}{T_1} - \frac{1}{T_2} \right) \] Substitute the known values: \[ \ln 2 = \frac{E_a}{8.314} \left( \frac{1}{298} - \frac{1}{308} \right) \] Solving for \(E_a\): \[ E_a = 48 \, \text{kJ/mol} \]
The following data were obtained during the first order thermal decomposition of \( \text{N}_2\text{O}_5(g) \) at constant volume: