Step 1: Understand the relationship between solubility product and electrode potential.
The relationship between the solubility product (\( K_{\text{sp}} \)) and the electrode potential can be derived using the Nernst equation. The equation for the half-cell reaction is:
\[
E = E^{\circ} - \frac{0.0591}{n} \log Q
\]
where:
- \( E^{\circ} \) is the standard electrode potential,
- \( n \) is the number of electrons involved in the reaction,
- \( Q \) is the reaction quotient.
Step 2: Calculate the solubility from the solubility product.
For the dissociation of \( \text{MX}(s) \) in water, the solubility product is:
\[
K_{\text{sp}} = [\text{M}^{+}][\text{X}^{-}] = s^2
\]
where \( s \) is the solubility. Given \( K_{\text{sp}} = 10^{-10} \), we can solve for \( s \):
\[
s = \sqrt{K_{\text{sp}}} = \sqrt{10^{-10}} = 10^{-5} \, \text{mol/L}
\]
Step 3: Apply the Nernst equation.
For the reaction:
\[
\text{M}^{+} + \text{X}^{-} \rightleftharpoons \text{MX}(s)
\]
we know that the standard electrode potential for the oxidation of \( \text{M}^{+} \) to \( \text{M} \) is \( E^{\circ}_{\text{M}^{+}/\text{M}} = 0.71 \, \text{V} \). The Nernst equation for the reverse reaction (reduction of \( \text{MX}^{-} \)) is:
\[
E = E^{\circ} - \frac{0.0591}{1} \log \left( \frac{1}{s^2} \right)
\]
Substituting \( s = 10^{-5} \):
\[
E = 0.71 \, \text{V} - \frac{0.0591}{1} \log \left( \frac{1}{(10^{-5})^2} \right)
\]
\[
E = 0.71 \, \text{V} - 0.0591 \log(10^{10})
\]
\[
E = 0.71 \, \text{V} - 0.0591 \times 10
\]
\[
E = 0.71 \, \text{V} - 0.591
\]
\[
E = 0.119 \, \text{V}
\]
Thus, \( E^{\circ}_{\text{M}/\text{MX}^{-}} = -0.119 \, \text{V} \).