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Explain why cell potentials are not multiplied by the coefficients in the balanced redox equation. (Use the relationship between \(\Delta G\) and cell potential to do this.)

Short Answer

Expert verified
In conclusion, cell potentials are not multiplied by the coefficients in the balanced redox equation because they are intensive properties, meaning they do not depend on the amounts of substances involved in the reaction. Additionally, the relationship between Gibbs Free Energy (ΔG) and cell potential (E) is given by ΔG = -nFE, which does not involve the stoichiometric coefficients. When the entire redox equation is multiplied by a factor k, the cell potential E remains unchanged, and the new ΔG is simply k times the original ΔG.

Step by step solution

01

Recall the relationship between ΔG and cell potential E

The relationship between Gibbs Free Energy (ΔG) and cell potential (E) is given by the following formula: \[ΔG = -nFE\] where: - ΔG is the Gibbs Free Energy (in joules or J), - n is the number of moles of electrons transferred in the redox reaction, - F is the Faraday's constant (96,485 C/mol), and - E is the cell potential (in volts or V).
02

Understand the meaning of cell potential E

The cell potential E is the difference in potential energy between the two half-reactions of a redox reaction. It determines the capacity of the redox reaction to do work. E is an intensive property, which means it does not depend on the amount or extent of the substances involved in the reaction. It is measured in volts (V) and is independent of the coefficients in the balanced redox equation.
03

Show how coefficients in the balanced redox equation affect ΔG

Now, let's analyze a generic balanced redox equation, given by: \(aA + bB \rightarrow cC + dD\) According to the stoichiometric coefficients (a, b, c, and d), the reaction can be written in terms of two half-reactions: Reduction: \(aA + ne^{-} \rightarrow bB\) Oxidation: \(cC \rightarrow dD + ne^{-}\) Now, let's calculate the Gibbs Free Energy change (ΔG) for the entire redox reaction. If we multiply the balanced redox equation by any factor k, the reaction would become: \(kaA + kbB \rightarrow kcC + kdD\) Notice that when we multiply the entire redox equation by k, it affects the number of moles of electrons transferred in the reaction as well. The new n would be kn. The ΔG for the new reaction is given by: \[ΔG' = -k \cdot n \cdot F \cdot E\] Since k is constant, and E remains the same (as it does not depend on the coefficients in the balanced redox equation), the new ΔG' is just k times the original ΔG: \[ΔG' = k \cdot ΔG\]
04

Conclude why cell potentials are not multiplied by coefficients in the balanced redox equation

As shown above, the cell potential E remains the same for the redox reaction despite the coefficients being multiplied by k. This is because E is an intensive property that is independent of the amounts of substances involved in the reaction. Also, the relationship between ΔG and E, given by ΔG = -nFE, is not affected by the stoichiometric coefficients in the balanced redox equation. Thus, it is clear that cell potentials are not multiplied by the coefficients in the balanced redox equation due to their independence from the amounts of substances and their direct relationship with ΔG.

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Most popular questions from this chapter

In 1973 the wreckage of the Civil War ironclad USS Monitor was discovered near Cape Hatteras, North Carolina. [The Monitor and the CSS Virginia (formerly the USS Merrimack) fought the first battle between iron-armored ships.] In 1987 investigations were begun to see if the ship could be salvaged. It was reported in Time (June \(22,1987)\) that scientists were considering adding sacrificial anodes of zinc to the rapidly corroding metal hull of the Monitor. Describe how attaching zinc to the hull would protect the Monitor from further corrosion.

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 \(\mathscr{C}_{\text {cell }}\) at \(25^{\circ} \mathrm{C}\) when \(\left[\mathrm{Zn}^{2+}\right]=0.10 \mathrm{M}\) and \(\left[\mathrm{Fe}^{2+}\right]=1.0 \times 10^{-5} \mathrm{M}\)

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 \(10.0 \mathrm{h}\). (Assume each half-cell contains \(1.00 \mathrm{L}\) of solution.) c. Calculate the mass of each electrode after \(10.0 \mathrm{h}\). d. How long can this battery deliver a current of 10.0 A before it goes dead?

The ultimate electron acceptor in the respiration process is molecular oxygen. Electron transfer through the respiratory chain takes place through a complex series of oxidationreduction reactions. Some of the electron transport steps use iron-containing proteins called cytochromes. All cytochromes transport electrons by converting the iron in the cytochromes from the +3 to the +2 oxidation state. Consider the following reduction potentials for three different cytochromes used in the transfer process of electrons to oxygen (the potentials have been corrected for \(\mathrm{pH}\) and for temperature): $$\begin{aligned} &\text { cytochrome } \mathrm{a}\left(\mathrm{Fe}^{3+}\right)+\mathrm{e}^{-} \longrightarrow \text { cytochrome } \mathrm{a}\left(\mathrm{Fe}^{2+}\right)\ &\mathscr{E}^{\circ}=0.385 \mathrm{V}\\\ &\text { cytochrome } \mathbf{b}\left(\mathrm{Fe}^{3+}\right)+\mathrm{e}^{-} \longrightarrow \text { cytochrome } \mathrm{b}\left(\mathrm{Fe}^{2+}\right)\ &\mathscr{E}^{\circ}=0.030 \mathrm{V}\\\ &\text { cytochrome } c\left(\mathrm{Fe}^{3+}\right)+\mathrm{e}^{-} \longrightarrow \text { cytochrome } \mathrm{c}\left(\mathrm{Fe}^{2+}\right)\ &\mathscr{E}^{\circ}=0.254 \mathrm{V} \end{aligned}$$ In the electron transfer series, electrons are transferred from one cytochrome to another. Using this information, determine the cytochrome order necessary for spontaneous transport of electrons from one cytochrome to another, which eventually will lead to electron transfer to \(\mathrm{O}_{2}\)

Sketch the galvanic cells based on the following half-reactions. Show the direction of electron flow, show the direction of ion migration through the salt bridge, and identify the cathode and anode. Give the overall balanced equation, and determine \(\mathscr{C}^{\circ}\) for the galvanic cells. Assume that all concentrations are \(1.0 M\) and that all partial pressures are 1.0 atm. a. \(\mathrm{H}_{2} \mathrm{O}_{2}+2 \mathrm{H}^{+}+2 \mathrm{e}^{-} \rightarrow 2 \mathrm{H}_{2} \mathrm{O} \quad \mathscr{E}^{\circ}=1.78 \mathrm{V}\) \(\mathrm{O}_{2}+2 \mathrm{H}^{+}+2 \mathrm{e}^{-} \rightarrow \mathrm{H}_{2} \mathrm{O}_{2} \quad \quad \mathscr{E}^{\circ}=0.68 \mathrm{V}\) b. \(\mathrm{Mn}^{2+}+2 \mathrm{e}^{-} \rightarrow \mathrm{Mn} \quad \mathscr{E}^{\circ}=-1.18 \mathrm{V}\) \(\mathrm{Fe}^{3+}+3 \mathrm{e}^{-} \rightarrow \mathrm{Fe} \quad \mathscr{E}^{\circ}=-0.036 \mathrm{V}\)

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