Which of the following relation represents correct relation between standard electrode potential and equilibrium constant?
I. `logK = (nFE^(@))/(2.303RT)`
II. `K = e^((nFE)/(RT))`
III. `log K = (-nFE^(@))/(2.303 RT)`
IV. `log K = 0.4342 (nFE^(@))/(RT)`
Choose the correct statement(s).
Which of the following relation represents correct relation between standard electrode potential and equilibrium constant?
I. `logK = (nFE^(@))/(2.303RT)`
II. `K = e^((nFE)/(RT))`
III. `log K = (-nFE^(@))/(2.303 RT)`
IV. `log K = 0.4342 (nFE^(@))/(RT)`
Choose the correct statement(s).
I. `logK = (nFE^(@))/(2.303RT)`
II. `K = e^((nFE)/(RT))`
III. `log K = (-nFE^(@))/(2.303 RT)`
IV. `log K = 0.4342 (nFE^(@))/(RT)`
Choose the correct statement(s).
A
I, II and III are correct
B
II and III are correct
C
I, II and IV are correct
D
I and IV are correct
Text Solution
AI Generated Solution
The correct Answer is:
To solve the problem, we need to analyze the relationships between standard electrode potential (E°), Gibbs free energy (ΔG), and the equilibrium constant (K).
### Step-by-Step Solution:
1. **Understand the Relationship between ΔG and E°**:
The Gibbs free energy change for a reaction can be expressed in terms of the standard electrode potential as:
\[
\Delta G = -nFE^0
\]
where:
- \( n \) = number of moles of electrons transferred
- \( F \) = Faraday's constant (approximately 96485 C/mol)
- \( E^0 \) = standard electrode potential
2. **Understand the Relationship between ΔG and K**:
The Gibbs free energy change is also related to the equilibrium constant by the equation:
\[
\Delta G = -2.303RT \log K
\]
where:
- \( R \) = universal gas constant (approximately 8.314 J/(mol·K))
- \( T \) = temperature in Kelvin
3. **Set the Two Expressions for ΔG Equal**:
Since both expressions represent ΔG, we can set them equal to each other:
\[
-nFE^0 = -2.303RT \log K
\]
4. **Rearranging the Equation**:
By cancelling the negative signs, we can rearrange the equation to solve for \( \log K \):
\[
nFE^0 = 2.303RT \log K
\]
Dividing both sides by \( 2.303RT \):
\[
\log K = \frac{nFE^0}{2.303RT}
\]
This corresponds to the first statement.
5. **Convert to Natural Log (ln)**:
We can also express \( K \) in terms of the natural logarithm:
\[
\Delta G = -RT \ln K
\]
Setting this equal to the first expression for ΔG:
\[
-nFE^0 = -RT \ln K
\]
Rearranging gives:
\[
nFE^0 = RT \ln K
\]
Dividing both sides by \( RT \):
\[
\ln K = \frac{nFE^0}{RT}
\]
Exponentiating both sides gives:
\[
K = e^{\frac{nFE^0}{RT}}
\]
This corresponds to the second statement.
6. **Check the Third Statement**:
The third statement is:
\[
\log K = \frac{-nFE^0}{2.303RT}
\]
This is incorrect because we derived that \( \log K \) is positive, not negative.
7. **Check the Fourth Statement**:
The fourth statement is:
\[
\log K = 0.4342 \frac{nFE^0}{RT}
\]
We can convert \( \frac{1}{2.303} \) to \( 0.4342 \) (since \( 0.4342 \approx \frac{1}{2.303} \)). Thus, this statement is also correct.
### Conclusion:
The correct statements are:
- I: \( \log K = \frac{nFE^0}{2.303RT} \) (Correct)
- II: \( K = e^{\frac{nFE^0}{RT}} \) (Correct)
- III: \( \log K = \frac{-nFE^0}{2.303RT} \) (Incorrect)
- IV: \( \log K = 0.4342 \frac{nFE^0}{RT} \) (Correct)
Thus, the correct options are I, II, and IV.
To solve the problem, we need to analyze the relationships between standard electrode potential (E°), Gibbs free energy (ΔG), and the equilibrium constant (K).
### Step-by-Step Solution:
1. **Understand the Relationship between ΔG and E°**:
The Gibbs free energy change for a reaction can be expressed in terms of the standard electrode potential as:
\[
\Delta G = -nFE^0
...
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