Step 1: Use the Arrhenius Equation.
The Arrhenius equation relates the rate constant (\(k\)) of a reaction to the temperature and activation energy (\(E_a\)):
\[
k = A e^{-\frac{E_a}{RT}}
\]
where:
- \( k \) = rate constant,
- \( A \) = pre-exponential factor,
- \( E_a \) = activation energy,
- \( R \) = universal gas constant (8.314 J/mol·K),
- \( T \) = temperature in Kelvin.
Step 2: Use the Integrated Form of the Arrhenius Equation.
We are given that the rate of the reaction doubles when the temperature increases from 298 K to 308 K. To calculate the activation energy, we can use the following form of the Arrhenius equation:
\[
\frac{k_2}{k_1} = e^{\frac{E_a}{R} \left( \frac{1}{T_1} - \frac{1}{T_2} \right)}
\]
where:
- \( k_2 \) and \( k_1 \) are the rate constants at temperatures \( T_2 \) and \( T_1 \), respectively,
- \( T_1 = 298 \, \text{K} \) and \( T_2 = 308 \, \text{K} \).
We are also given that \( k_2 = 2k_1 \), so:
\[
2 = e^{\frac{E_a}{8.314} \left( \frac{1}{298} - \frac{1}{308} \right)}
\]
Step 3: Solve for Activation Energy.
Taking the natural logarithm of both sides:
\[
\log 2 = \frac{E_a}{8.314} \left( \frac{1}{298} - \frac{1}{308} \right)
\]
Substitute \( \log 2 = 0.30 \) and calculate the difference in reciprocals of temperatures:
\[
\frac{1}{298} - \frac{1}{308} = \frac{308 - 298}{298 \times 308} = \frac{10}{91704} \approx 1.091 \times 10^{-4}
\]
Now substitute these values into the equation:
\[
0.30 = \frac{E_a}{8.314} \times 1.091 \times 10^{-4}
\]
Solving for \( E_a \):
\[
E_a = \frac{0.30 \times 8.314}{1.091 \times 10^{-4}} \approx 53 \, \text{kJ/mol}
\]
Conclusion.
The activation energy (\(E_a\)) for this reaction is approximately 53 kJ/mol.