The rate constant k for a certain reaction is measured at two different temperatures: temperature k 248.0 °C 9.9 × 108 169.0 °C 9.8 x 10² Assuming the rate constant obeys the Arrhenius equation, calculate the activation energy E for this reaction. Round your answer to 2 significant digits. kJ E = mol Ś ? 0 x10 X

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In this exercise, you will learn how to calculate the activation energy (Ea) of a reaction using the Arrhenius equation. The rate constant \( k \) for a certain reaction is measured at two different temperatures, as shown in the table below:

\[
\begin{array}{|c|c|}
\hline
\text{temperature} & k \\
\hline
248.0 \, ^\circ \text{C} & 9.9 \times 10^8 \\
169.0 \, ^\circ \text{C} & 9.8 \times 10^7 \\
\hline
\end{array}
\]

To calculate the activation energy \( E_a \) for this reaction, we will assume the rate constant obeys 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.

Given:
- The temperatures are 248.0°C and 169.0°C, which need to be converted to Kelvin (K):
  - \( 248.0°C + 273.15 = 521.15 \, K \)
  - \( 169.0°C + 273.15 = 442.15 \, K \)

- The rate constants \( k \) at these temperatures are:
  - \( k_1 = 9.9 \times 10^8 \) at \( T_1 = 521.15 \, K \)
  - \( k_2 = 9.8 \times 10^7 \) at \( T_2 = 442.15 \, K \)

Using the logarithmic form of the Arrhenius equation:

\[
\ln \left( \frac{k_2}{k_1} \right) = - \frac{E_a}{R} \left( \frac{1}{T_2} - \frac{1}{T_1} \right)
\]

Rearranging to solve for \( E_a \):

\[
E_a = - R \frac{\ln \
Transcribed Image Text:In this exercise, you will learn how to calculate the activation energy (Ea) of a reaction using the Arrhenius equation. The rate constant \( k \) for a certain reaction is measured at two different temperatures, as shown in the table below: \[ \begin{array}{|c|c|} \hline \text{temperature} & k \\ \hline 248.0 \, ^\circ \text{C} & 9.9 \times 10^8 \\ 169.0 \, ^\circ \text{C} & 9.8 \times 10^7 \\ \hline \end{array} \] To calculate the activation energy \( E_a \) for this reaction, we will assume the rate constant obeys 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. Given: - The temperatures are 248.0°C and 169.0°C, which need to be converted to Kelvin (K): - \( 248.0°C + 273.15 = 521.15 \, K \) - \( 169.0°C + 273.15 = 442.15 \, K \) - The rate constants \( k \) at these temperatures are: - \( k_1 = 9.9 \times 10^8 \) at \( T_1 = 521.15 \, K \) - \( k_2 = 9.8 \times 10^7 \) at \( T_2 = 442.15 \, K \) Using the logarithmic form of the Arrhenius equation: \[ \ln \left( \frac{k_2}{k_1} \right) = - \frac{E_a}{R} \left( \frac{1}{T_2} - \frac{1}{T_1} \right) \] Rearranging to solve for \( E_a \): \[ E_a = - R \frac{\ln \
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