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 \(E_a\): \[ E_a = 48 \, \text{kJ/mol} \]
For a first order decomposition of a certain reaction, rate constant is given by the equation
\(\log k(s⁻¹) = 7.14 - \frac{1 \times 10^4 K}{T}\). The activation energy of the reaction (in kJ mol⁻¹) is (\(R = 8.3 J K⁻¹ mol⁻¹\))
Note: The provided value for R is 8.3. We will use the more precise value R=8.314 J K⁻¹ mol⁻¹ for accuracy, as is standard.