
Given Information:
Overall rate constant: \( K = \frac{k_1 k_2}{k_3} \)
Overall activation energy: \( E_a = 400 \, \text{kJ/mol} \)
Activation energies for each step:
\( E_{a1} = 300 \, \text{kJ/mol}, \, E_{a2} = 200 \, \text{kJ/mol}, \, E_{a3} = ? \)
Using the Arrhenius Equation:
The overall rate constant \( K \) and overall activation energy \( E_a \) can be determined by combining the individual rate constants and activation energies as follows:
\[ K = \frac{k_1 k_2}{k_3} \]
According to the Arrhenius equation, we can write: \[ \ln K = \ln \left(\frac{k_1 k_2}{k_3}\right) = \ln k_1 + \ln k_2 - \ln k_3 \] The corresponding activation energy \( E_a \) for \( K \) is: \[ E_a = E_{a1} + E_{a2} - E_{a3} \]
Substituting the Given Values:
\[ 400 = 300 + 200 - E_{a3} \]
Solving for \( E_{a3} \):
\[ E_{a3} = 500 - 400 = 100 \, \text{kJ/mol} \]
Conclusion:
The value of \( E_{a3} \) is \( 100 \, \text{kJ/mol} \).
For the reaction \( A + B \to C \), the rate law is found to be \( \text{rate} = k[A]^2[B] \). If the concentration of \( A \) is doubled and \( B \) is halved, by what factor does the rate change?


In the first configuration (1) as shown in the figure, four identical charges \( q_0 \) are kept at the corners A, B, C and D of square of side length \( a \). In the second configuration (2), the same charges are shifted to mid points C, E, H, and F of the square. If \( K = \frac{1}{4\pi \epsilon_0} \), the difference between the potential energies of configuration (2) and (1) is given by: