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If the equilibrium constant for a two-electron redox reaction at \(298 \mathrm{~K}\) is \(1.5 \times 10^{-4}\), calculate the corresponding \(\Delta G^{\circ}\) and \(E_{\text {cell }}^{\circ}\).

Short Answer

Expert verified
Using the given equilibrium constant (K=1.5 x 10⁻⁴) and temperature (298 K), we calculate the corresponding Gibbs free energy change (ΔG°) using the formula ΔG° = -RT ln(K), which yields ΔG° = 32,839.57 J/mol. We then use the formula ΔG° = -nFE°₈cell to find the standard cell potential (E°₈cell), resulting in E°₈cell = -0.17 V.

Step by step solution

01

Calculate ΔG° using the equilibrium constant

We can use the given equilibrium constant (K=1.5 x 10⁻⁴) and the formula ΔG° = -RT ln(K) to find the Gibbs free energy change. First, plug in the values for R (8.314 J/mol·K) and T (298 K) into the formula: ΔG° = - (8.314 J/mol·K) x (298 K) x ln(1.5 x 10⁻⁴) Now, calculate the natural logarithm of K: ln(1.5 x 10⁻⁴) = -13.41 So, we can plug this value back into the formula for ΔG° : ΔG° = - (8.314 J/mol·K) x (298 K) x (-13.41) Finally, calculate the value of ΔG° : ΔG° = 32839.57 J/mol
02

Calculate E°₈cell using the ΔG° value

Now that we have the value for ΔG°, we can use the formula ΔG° = -nFE°₈cell to find the standard cell potential. First, plug in the values for n (2) and F (96485 C/mol) into the formula: 32839.57 J/mol = - (2) x (96485 C/mol) x E°₈cell Now, isolate E°₈cell by dividing both sides by -2F: E°₈cell = (32839.57 J/mol) / (-2 x 96485 C/mol) Finally, calculate the value of E°₈cell : E°₈cell = -0.17 V So, the corresponding Gibbs free energy change (ΔG°) is 32,839.57 J/mol, and the standard cell potential (E°₈cell) is -0.17 V.

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Most popular questions from this chapter

Complete and balance the following half-reactions. In each case indicate whether the half-reaction is an oxidation or a reduction. (a) \(\mathrm{Mo}^{3+}(a q) \longrightarrow \mathrm{Mo}(s)\) (acidic or basic solution) (b) \(\mathrm{H}_{2} \mathrm{SO}_{3}(a q)--\rightarrow \mathrm{SO}_{4}^{2-}(a q)\) (acidic solution) (c) \(\mathrm{NO}_{3}^{-}(a q)-\cdots \rightarrow \mathrm{NO}(g)\) (acidic solution) (d) \(\mathrm{O}_{2}(\mathrm{~g})-\longrightarrow \mathrm{H}_{2} \mathrm{O}(l)\) (acidic solution) (e) \(\mathrm{Mn}^{2+}(a q)-\rightarrow \rightarrow \mathrm{MnO}_{2}(s)\) (basic solution) (f) \(\mathrm{Cr}(\mathrm{OH})_{3}(s)-\cdots \mathrm{CrO}_{4}^{2-}(a q)\) (basic solution) (g) \(\mathrm{O}_{2}(g) \longrightarrow \mathrm{H}_{2} \mathrm{O}(l)\) (basic solution)

A voltaic cell is constructed that uses the following halfcell reactions: $$ \begin{gathered} \mathrm{Cu}^{+}(a q)+\mathrm{e}^{-} \longrightarrow \mathrm{Cu}(s) \\ \mathrm{I}_{2}(s)+2 \mathrm{e}^{-} \longrightarrow 2 \mathrm{I}^{-}(a q) \end{gathered} $$ The cell is operated at \(298 \mathrm{~K}\) with \(\left[\mathrm{Cu}^{+}\right]=0.25 \mathrm{M}\) and \(\left[\mathrm{I}^{-}\right]=3.5 \mathrm{M}\). (a) Determine \(E\) for the cell at these concentrations. (b) Which electrode is the anode of the cell? (c) Is the answer to part (b) the same as it would be if the cell were operated under standard conditions? (d) If \(\left[\mathrm{Cu}^{+}\right]\) was equal to \(0.15 \mathrm{M}\), at what concentration of \(\mathrm{I}^{-}\) would the cell have zero potential?

A voltaic cell is constructed that uses the following reaction and operates at \(298 \mathrm{~K}\) : $$ \mathrm{Zn}(s)+\mathrm{Ni}^{2+}(a q) \longrightarrow \mathrm{Zn}^{2+}(a q)+\mathrm{Ni}(s) $$ (a) What is the emf of this cell under standard conditions? (b) What is the emf of this cell when \(\left[\mathrm{Ni}^{2+}\right]=3.00 \mathrm{M}\) and \(\left[\mathrm{Zn}^{2+}\right]=0.100 \mathrm{M} ?\) (c) What is the emf of the cell when \(\left[\mathrm{Ni}^{2+}\right]=0.200 M\), and \(\left[\mathrm{Zn}^{2+}\right]=0.900 \mathrm{M} ?\)

(a) What is a standard reduction potential? (b) What is the standard reduction potential of a standard hydrogen electrode?

(a) \(\mathrm{A} \mathrm{Cr}^{3+}(a q)\) solution is electrolyzed, using a current of \(7.60 \mathrm{~A}\). What mass of \(\mathrm{Cr}(s)\) is plated out after \(2.00\) days? (b) What amperage is required to plate out \(0.250 \mathrm{~mol} \mathrm{Cr}\) from a \(\mathrm{Cr}^{3+}\) solution in a period of \(8.00 \mathrm{~h}\) ?

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