The standard Gibbs free energy change (\( \Delta G^\circ \)) for the reaction can be calculated using the equation:
\[
\Delta G^\circ = -nF E^\circ
\]
where:
- \( n \) is the number of moles of electrons involved in the reaction (for this reaction, \( n = 2 \)),
- \( F \) is Faraday’s constant (96500 C mol\(^{-1}\)),
- \( E^\circ \) is the cell potential.
The cell potential (\( E^\circ_{{cell}} \)) is calculated by:
\[
E^\circ_{{cell}} = E^\circ_{{cathode}} - E^\circ_{{anode}}
\]
Since the reduction reaction is at the cathode and oxidation is at the anode, we take the reduction potentials for the half-reactions.
Here, Mg will be oxidized (anode) and Cd\(^{2+}\) will be reduced (cathode). Therefore:
\[
E^\circ_{{cell}} = 0.403 \, {V} - 2.37 \, {V} = -1.967 \, {V}
\]
Now, calculating \( \Delta G^\circ \):
\[
\Delta G^\circ = -2 \times 96500 \times (-1.967) = 379,745 \, {J} = 379.7 \, {kJ}
\]
So the Gibbs free energy change is approximately between -381 kJ to -379 kJ.