The standard redox potential values for two half-reactions are given below. The value for Faraday’s constant is 96.48 kJ V-1 mol-1 and Gas constant R is 8.3 J K-1 mol-1. NAD+ + H+ + 2e- → NADH    E° = −0.315 V FAD + 2H+ + 2e- → FADH2    E° = −0.219 V Q.52 The ΔG° for the oxidation of NADH by FAD is Options: (A) −9.25 kJ mol-1 (B) −103.04 kJ mol-1 (C) +51.52 kJ mol-1 (D) −18.5 kJ mol-1

The standard redox potential values for two half-reactions are given below.
The value for Faraday’s constant is 96.48 kJ V-1 mol-1 and
Gas constant R is 8.3 J K-1 mol-1.

NAD+ + H+ + 2e → NADH    E° = −0.315 V
FAD + 2H+ + 2e → FADH2    E° = −0.219 V

Q.52

The ΔG° for the oxidation of NADH by FAD is

Options:

(A) −9.25 kJ mol-1

(B) −103.04 kJ mol-1

(C) +51.52 kJ mol-1

(D) −18.5 kJ mol-1

ΔG° for Oxidation of NADH by FAD

Redox reactions involving biological molecules such as NADH and
FAD are fundamental in bioenergetics. This problem evaluates the
relationship between standard redox potential (E°) and Gibbs free energy
change (ΔG°).

Given Data

Standard Reduction Half-Reactions:

NAD+ + H+ + 2e → NADH
E° = −0.315 V

FAD + 2H+ + 2e → FADH2
E° = −0.219 V

Constants:
Faraday constant (F) = 96.48 kJ V−1 mol−1
Number of electrons transferred (n) = 2

Step 1: Identify Oxidation and Reduction

  • NADH is oxidized to NAD+
  • FAD is reduced to FADH2

Step 2: Calculate Cell Potential (E°cell)

E°cell = E°cathode − E°anode

E°cell = (−0.219) − (−0.315) = +0.096 V

Step 3: Calculate ΔG°

ΔG° = −nFE°cell

ΔG° = −(2)(96.48)(0.096)

ΔG° = −18.5 kJ mol−1

Correct Answer

Option (D): −18.5 kJ mol−1

Explanation of All Options

Option (A): −9.25 kJ mol−1
Incorrect due to assuming transfer of only one electron instead of two.

Option (B): −103.04 kJ mol−1
Value is too large and does not match the given redox potential difference.

Option (C): +51.52 kJ mol−1
Positive ΔG° indicates a non-spontaneous reaction, which is incorrect here.

Option (D): −18.5 kJ mol−1
Correct calculation using ΔG° = −nFE°cell.

Conclusion

The oxidation of NADH by FAD is a spontaneous process with a negative Gibbs free
energy change:

ΔG° = −18.5 kJ mol−1

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