
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 \( 100 \, \text{kJ/mol} \).
Reactant ‘A’ underwent a decomposition reaction. The concentration of ‘A’ was measured periodically and recorded in the table given below:
Based on the above data, predict the order of the reaction and write the expression for the rate law.
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.
In the circuit shown, assuming the threshold voltage of the diode is negligibly small, then the voltage \( V_{AB} \) is correctly represented by: