The equation \(\Delta G^{\circ}=-\mathrm{nF} \mathscr{E}^{\circ}\) also can be applied to half-reactions. Use standard reduction potentials to estimate \(\Delta G_{\mathrm{f}}^{\circ}\) for \(\mathrm{Fe}^{2+}(a q)\) and $\mathrm{Fe}^{3+}(a q) .\left(\Delta G_{\mathrm{f}}^{\circ} \text { for } \mathrm{e}^{-}=0 .\right)$

Short Answer

Expert verified
The standard Gibbs free energies of formation for \(\mathrm{Fe}^{2+}(\mathrm{aq})\) and \(\mathrm{Fe}^{3+}(\mathrm{aq})\) ions are approximately \(8.48 \times 10^4\, \mathrm{J/mol}\) and \(1.19 \times 10^4\, \mathrm{J/mol}\) respectively.

Step by step solution

01

Write the half-reactions for the formation of iron ions

We need to find the half-reactions for the formation of \(\mathrm{Fe}^{2+}(\mathrm{aq})\) and \(\mathrm{Fe}^{3+}(\mathrm{aq})\) ions. The half-reactions are: For \(\mathrm{Fe}^{2+}(\mathrm{aq})\) formation: \[\mathrm{Fe}(s) \rightarrow \mathrm{Fe}^{2+}(\mathrm{aq}) + 2\mathrm{e}^-\] For \(\mathrm{Fe}^{3+}(\mathrm{aq})\) formation: \[\mathrm{Fe}(s) \rightarrow \mathrm{Fe}^{3+}(\mathrm{aq}) + 3\mathrm{e}^-\]
02

Find the number of electrons exchanged for each half-reaction

The number of electrons exchanged for each half-reaction is determined by the number of electrons released during the oxidation process. From the half-reactions above, we can see that: For \(\mathrm{Fe}^{2+}(\mathrm{aq})\) formation: \(n = 2\) For \(\mathrm{Fe}^{3+}(\mathrm{aq})\) formation: \(n = 3\)
03

Look up the standard reduction potentials for each half-reaction

We will consult a standard reduction potential table to find the standard reduction potentials (\(\mathscr{E}^\circ\)) for both half-reactions: For \(\mathrm{Fe}^{2+}\) formation: \(\mathscr{E}^\circ (\mathrm{Fe}^{2+}) = -0.44 \,\mathrm{V}\) For \(\mathrm{Fe}^{3+}\) formation: \(\mathscr{E}^\circ (\mathrm{Fe}^{3+}) = -0.041\,\mathrm{V}\)
04

Calculate the standard Gibbs free energy of formation for each iron ion

Now, we will use the given equation, \(\Delta G^\circ = -nF\mathscr{E}^\circ\), and plug in the values determined in Steps 1-3 to calculate the standard Gibbs free energy of formation (\(\Delta G_{\mathrm{f}}^\circ\)) for each iron ion: For \(\mathrm{Fe}^{2+}(\mathrm{aq})\): \[\Delta G_{\mathrm{f}}^\circ(\mathrm{Fe}^{2+}) = -2 \times \mathrm{F} \times (-0.44\,\mathrm{V})\] For \(\mathrm{Fe}^{3+}(\mathrm{aq})\): \[\Delta G_{\mathrm{f}}^\circ(\mathrm{Fe}^{3+}) = -3 \times \mathrm{F} \times (-0.041\,\mathrm{V})\] Where Faraday's constant F is approximately \(96485\, \mathrm{C/mol}\). Calculating the \(\Delta G_{\mathrm{f}}^\circ\) values: \[\Delta G_{\mathrm{f}}^\circ(\mathrm{Fe}^{2+}) \approx 8.48 \times 10^4 \, \mathrm{J/mol}\] \[\Delta G_{\mathrm{f}}^\circ(\mathrm{Fe}^{3+}) \approx 1.19 \times 10^4 \, \mathrm{J/mol}\] Therefore, the standard Gibbs free energies of formation for \(\mathrm{Fe}^{2+}(\mathrm{aq})\) and \(\mathrm{Fe}^{3+}(\mathrm{aq})\) are approximately \(8.48 \times 10^4\, \mathrm{J/mol}\) and \(1.19 \times 10^4\, \mathrm{J/mol}\) respectively.

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Most popular questions from this chapter

A zinc-copper battery is constructed as follows at \(25^{\circ} \mathrm{C} :\) $$\mathrm{Zn}\left|\mathrm{Zn}^{2+}(0.10 M)\right|\left|\mathrm{Cu}^{2+}(2.50 M)\right| \mathrm{Cu}$$ The mass of each electrode is 200. g. a. Calculate the cell potential when this battery is first connected. b. Calculate the cell potential after 10.0 A of current has flowed for 10.0 h. (Assume each half-cell contains 1.00 L of solution.) c. Calculate the mass of each electrode after 10.0 h. d. How long can this battery deliver a current of 10.0 A before it goes dead?

Consider the galvanic cell based on the following halfreactions: $$\begin{array}{ll}{\mathrm{Zn}^{2+}+2 \mathrm{e}^{-} \longrightarrow \mathrm{Zn}} & {\mathscr{E}^{\circ}=-0.76 \mathrm{V}} \\ {\mathrm{Fe}^{2+}+2 \mathrm{e}^{-} \longrightarrow \mathrm{Fe}} & {\mathscr{E}^{\circ}=-0.44 \mathrm{V}}\end{array}$$ a. Determine the overall cell reaction and calculate $\mathscr{E}_{\text { cell }}$ b. Calculate \(\Delta G^{\circ}\) and \(K\) for the cell reaction at $25^{\circ} \mathrm{C}$ c. Calculate \(\mathscr{E}_{\text { cell }}\) at \(25^{\circ} \mathrm{C}\) when \(\left[\mathrm{Zn}^{2+}\right]=0.10 M\) and $\left[\mathrm{Fe}^{2+}\right]=1.0 \times 10^{-5} \mathrm{M} .$

An aqueous solution of an unknown salt of ruthenium is electrolyzed by a current of 2.50 A passing for 50.0 min. If 2.618 g Ru is produced at the cathode, what is the charge on the ruthenium ions in solution?

If the cell potential is proportional to work and the standard reduction potential for the hydrogen ion is zero, does this mean that the reduction of the hydrogen ion requires no work?

Consider a galvanic cell based on the following half-reactions: $$\begin{array}{ll}{\text {}} & { \mathscr{E}^{\circ}(\mathbf{V}) } \\ \hline {\mathrm{La}^{3+}+3 \mathrm{e}^{-} \longrightarrow \mathrm{La}} & {-2.37} \\\ {\mathrm{Fe}^{2+}+2 \mathrm{e}^{-} \longrightarrow \mathrm{Fe}} & {-0.44}\end{array}$$ a. What is the expected cell potential with all components in their standard states? b. What is the oxidizing agent in the overall cell reaction? c. What substances make up the anode compartment? d. In the standard cell, in which direction do the electrons flow? e. How many electrons are transferred per unit of cell reaction? f. If this cell is set up at \(25^{\circ} \mathrm{C}\) with \(\left[\mathrm{Fe}^{2+}\right]=2.00 \times 10^{-4} M\) and \(\left[\mathrm{La}^{3+}\right]=3.00 \times 10^{-3} M,\) what is the expected cell potential?

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