To solve this problem, we will use the Nernst equation to determine the standard electrode potential of the ${(AgCl/Ag,Cl^{-})}$ electrode.
We are given a cell: ${ Pt(s) | H_2(g , 1 \text{ bar}) | HCl(aq) | AgCl | Ag(s) | Pt(s) } $ and the cell potential (Ecell) is 0.92 V.
The Nernst equation for the cell is:
E_{\text{cell}} = E^\circ_{\text{cell}} - \frac{0.06}{n} \log \frac{[HCl]}{P_{H_2}[Cl^-]}
We need to determine the standard electrode potential of the ${(AgCl/Ag,Cl^{-})}$ electrode, which is part of the cell.
The cell is composed of two half-cells:
The potential of the hydrogen electrode is 0 V under standard conditions.
At 298 K, ${\frac{2.303RT}{F} = 0.06 \, \text{V}} is given, and we have:
E_{\text{cell}} = E^\circ_{\text{cell}} - 0.06 \cdot \log \left( \frac{a_{Ag^+} a_{Cl^-}}{a_{H^+}^2}\right),
where a_{Ag^+} is the activity of silver ions, a_{Cl^-} is the activity of chloride ions, and a_{H^+} is the activity of hydrogen ions.
Given ${10^{-6}}$ molal HCl solution is used:
a_{H^+} = a_{Cl^-} = 10^{-6} \, \text{molal}
Substituting the values into the Nernst equation gives:
0.92 = E^\circ_{\text{cell}} - 0.06 \log \frac{(10^{-6})(10^{-6})}{(10^{-6})^2}
Simplifying:
0.92 = E^\circ_{\text{cell}}
The standard electrode potential of the ${(AgCl/Ag, Cl^-)}$ electrode is therefore:
0.20 V
The correct answer is 0.20 \, \text{V}.
\(Pt(s) ∣ H2(g)(1atm) ∣ H+(aq, [H+]=1)\, ∥\, Fe3+(aq), Fe2+(aq) ∣ Pt(s)\)
Given\( E^∘_{Fe^{3+}Fe^{2+}}\)\(=0.771V\) and \(E^∘_{H^{+1/2}H_2}=0\,V,T=298K\)
If the potential of the cell is 0.712V, the ratio of concentration of \(Fe2+\) to \(Fe3+\) is