Give step-by-step solution with explanation and final answer:2. (50pts) The rate constants for a bimolecular gas phase reaction, A + B — P. over a range of
temperatures is shown in the table below.
[mK T2905 [223 [218 [213 [206 [200 [195 |
K(10° dm’ 0.494) 0.452 0.379 0.295 0.241 0.217
mol! s™
Calculate the Gibbs free energy of activation for the given reaction at 298 K.
Question:
Give step-by-step solution with explanation and final answer:2. (50pts) The rate constants for a bimolecular gas phase reaction, A + B — P. over a range of
temperatures is shown in the table below.
[mK T2905 [223 [218 [213 [206 [200 [195 |
K(10° dm’ 0.494) 0.452 0.379 0.295 0.241 0.217
mol! s™
Calculate the Gibbs free energy of activation for the given reaction at 298 K.
This is AI generated Response.
Asked by: francis
Created at: 2025-12-14 01:51:35
Final Answer:
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Let's solve the problem step by step:
---
## **Step 1: Understanding the Problem**
We are given the rate constants (\( k \)) at different temperatures (\( T \)) for a bimolecular gas-phase reaction. We are asked to **calculate the Gibbs free energy of activation (\( \Delta G^\ddagger \)) at 298 K**.
---
## **Step 2: Key Equation - Eyring Equation**
The Eyring equation relates the rate constant to the Gibbs free energy of activation:
\[
k = \frac{k_B T}{h} e^{-\Delta G^\ddagger / RT}
\]
Where:
- \( k \) = rate constant
- \( k_B \) = Boltzmann constant (\(1.381 \times 10^{-23}\) J/K)
- \( h \) = Planck constant (\(6.626 \times 10^{-34}\) J·s)
- \( T \) = temperature (in K)
- \( R \) = gas constant (\(8.314\) J/(mol·K))
- \( \Delta G^\ddagger \) = Gibbs free energy of activation
---
## **Step 3: Rearranging for \(\Delta G^\ddagger\)**
Take the natural logarithm:
\[
\ln k = \ln\left(\frac{k_B T}{h}\right) - \frac{\Delta G^\ddagger}{RT}
\]
So,
\[
\Delta G^\ddagger = -RT \left[ \ln k - \ln\left(\frac{k_B T}{h}\right) \right]
\]
Or,
\[
\Delta G^\ddagger = RT \ln\left(\frac{k_B T}{h k}\right)
\]
---
## **Step 4: Plug in the Values**
Given:
- \( T = 298\, \text{K} \)
- \( k = 3.55 \times 10^6 \, \text{dm}^3\, \text{mol}^{-1}\,\text{s}^{-1} \)
- Convert \( k \) to SI units (\( \text{m}^3\,\text{mol}^{-1}\,\text{s}^{-1} \)): \( 1\,\text{dm}^3 = 10^{-3}\,\text{m}^3 \), so \( k = 3.55 \times 10^3\,\text{m}^3\,\text{mol}^{-1}\,\text{s}^{-1} \)
Constants:
- \( k_B = 1.381 \times 10^{-23}\,\text{J/K} \)
- \( h = 6.626 \times 10^{-34}\,\text{J·s} \)
- \( R = 8.314\,\text{J/(mol·K)} \)
---
## **Step 5: Calculation**
\[
\Delta G^\ddagger = RT \ln\left(\frac{k_B T}{h k}\right)
\]
Plug in values:
1. **Compute \(\frac{k_B T}{h k}\):**
\[
\frac{k_B \cdot T}{h \cdot k} = \frac{1.381 \times 10^{-23} \times 298}{6.626 \times 10^{-34} \times 3.55 \times 10^3}
\]
Numerator: \(1.381 \times 10^{-23} \times 298 = 4.11238 \times 10^{-21}\)
Denominator: \(6.626 \times 10^{-34} \times 3.55 \times 10^3 = 2.35223 \times 10^{-30}\)
So:
\[
\frac{4.11238 \times 10^{-21}}{2.35223 \times 10^{-30}} \approx 1.749 \times 10^9
\]
2. **Compute \(\ln(1.749 \times 10^9)\):**
\[
\ln(1.749 \times 10^9) = \ln(1.749) + \ln(10^9) \approx .560 + 20.723 = 21.283
\]
3. **Compute \(RT\):**
\[
RT = 8.314 \times 298 = 2477.572 \text{ J/mol}
\]
4. **Calculate \(\Delta G^\ddagger\):**
\[
\Delta G^\ddagger = 2477.572 \times 21.283 \approx 52744 \text{ J/mol} = 52.7 \text{ kJ/mol}
\]
---
## **Final Answer**
\[
\boxed{
\Delta G^\ddagger = 52.7 \ \text{ kJ/mol} \text{ at 298 K}
}
\]
---
### **Summary Table**
| Quantity | Value |
|-------------------------|------------------------|
| \( T \) | 298 K |
| \( k \) | \(3.55 \times 10^3\,\text{m}^3\,\text{mol}^{-1}\,\text{s}^{-1}\) |
| \( R \) | 8.314 J/(mol·K) |
| \( k_B \) | \(1.381 \times 10^{-23}\) J/K |
| \( h \) | \(6.626 \times 10^{-34}\) J·s |
| \( \Delta G^\ddagger \) | \(\mathbf{52.7~kJ/mol}\) |
---
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