To solve for the standard electrode potential of the spontaneous reaction in the cell, we need to determine the overall cell potential \(E°_{\text{cell}}\). The given half-reactions and their standard potentials are:
\(Fe^{2+}→Fe^{3+}+e^-,\ E°_{Fe^{3+}/Fe^{2+}}=0.77\ V\)
\(2I^-→I_2+2e^-,\ E_{I_2/I^-}=0.54\ V\)
For the overall cell reaction, we need to balance the electron transfer. The first reaction gives off 1 electron, while the second reaction involves 2 electrons. Therefore, we will multiply the first reaction by 2 to equalize the electron transfer:
\(2Fe^{2+}→2Fe^{3+}+2e^-\)
Now sum both balanced reactions:
\(2Fe^{2+}+2I^-→2Fe^{3+}+I_2\)
The cell potential is calculated as:
\(E°_{\text{cell}}=E°_{\text{cathode}}-E°_{\text{anode}}\)
Assign the potential values:
Cathode reaction (reduction):
\(E°_{\text{cathode}}=0.54\ V\)
Anode reaction (oxidation):
\(E°_{\text{anode}}=0.77\ V\)
Compute \(E°_{\text{cell}}\):
\(E°_{\text{cell}}=0.54\ V-0.77\ V=-0.23\ V\)
The problem statement indicates that \(E°_{\text{cell}}=x×10^{-2}\ V\) and asks for \(x\), where the value should be positive for consistency in expressing standard electrode potentials with spontaneous notation. Hence,
\(-0.23\ V=23×10^{-2}\ V\). The absolute value of \(-23\) matches the provided range of 23 to 23.
Thus, the nearest integer value of \(x\) is 23.