The rate of reaction doubles when the temperature is raised by 10°C. To find the activation energy \( E_a \), we use the Arrhenius equation:
\[
k = A e^{-\frac{E_a}{RT}}
\]
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),
- \( T \) is the temperature in Kelvin.
### Step 1: Relating Rate Constants at Two Temperatures
To calculate the activation energy when the rate constant doubles with a 10°C increase in temperature, we use the modified 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:
- \( k_1 \) and \( k_2 \) are the rate constants at temperatures \( T_1 \) and \( T_2 \), respectively,
- \( T_1 \) is the initial temperature,
- \( T_2 = T_1 + 10 \) (since the temperature is increased by 10°C).
Given that the rate doubles, we have:
\[
\frac{k_2}{k_1} = 2
\]
Substitute this into the equation:
\[
2 = e^{\frac{E_a}{R} \left( \frac{1}{T_1} - \frac{1}{T_1 + 10} \right)}
\]
### Step 2: Approximation for Small Temperature Change
For a small temperature change (in this case, 10°C), we can approximate the expression \( \frac{1}{T_1} - \frac{1}{T_1 + 10} \) using a first-order expansion:
\[
\frac{1}{T_1} - \frac{1}{T_1 + 10} \approx \frac{10}{T_1^2}
\]
Thus, the equation becomes:
\[
2 = e^{\frac{E_a}{R} \cdot \frac{10}{T_1^2}}
\]
### Step 3: Solving for \( E_a \)
To solve for \( E_a \), we take the natural logarithm of both sides:
\[
\ln(2) = \frac{E_a}{R} \cdot \frac{10}{T_1^2}
\]
\[
E_a = \frac{\ln(2) \cdot R \cdot T_1^2}{10}
\]
Using \( \ln(2) \approx 0.693 \) and \( R = 8.314 \, \text{J/mol·K} \), we can estimate the activation energy \( E_a \).
For typical reaction conditions, we assume \( T_1 \) around 300 K (about 27°C), which gives:
\[
E_a \approx \frac{0.693 \cdot 8.314 \cdot 300^2}{10} \approx 60 \, \text{kJ/mol}.
\]
Thus, the activation energy for this reaction is approximately 60 kJ/mol.