Consider the cell described below: $$\mathrm{Zn}\left|\mathrm{Zn}^{2+}(1.00 M) \| \mathrm{Cu}^{2+}(1.00 M)\right| \mathrm{Cu}$$ Calculate the cell potential after the reaction has operated long enough for the \(\left[\mathrm{Zn}^{2+}\right]\) to have changed by \(0.20 \mathrm{~mol} / \mathrm{L}\). (Assume \(\left.T=25^{\circ} \mathrm{C} .\right)\)

Short Answer

Expert verified
The cell potential after the reaction has operated long enough for the [Zn²⁺] to have changed by 0.20 mol/L is approximately \(1.079 V\).

Step by step solution

01

Identify the half-reactions

To calculate the cell potential, we need to identify the half-reactions occurring at the anode (Zn) and cathode (Cu). The balanced half-reactions are given below: At the anode (oxidation): \(Zn \rightarrow Zn^{2+} + 2e^-\) At the cathode (reduction): \(Cu^{2+} + 2e^- \rightarrow Cu\)
02

Write the overall cell reaction

The overall cell reaction is obtained by adding the balanced oxidation and reduction half-reactions: \(Zn + Cu^{2+} \rightarrow Zn^{2+} + Cu\)
03

Calculate the standard cell potential

To calculate the standard cell potential, we need to consult a table of standard electrode potentials and find the values for Zn²⁺/Zn and Cu²⁺/Cu half-cells: The standard reduction potentials are: \(E^0_{Zn^{2+}/Zn} = -0.76 V\) \(E^0_{Cu^{2+}/Cu} = +0.34 V\) Now, we can calculate the standard cell potential (\(E^0_{cell}\)): \(E^0_{cell} = E^0_{cathode} - E^0_{anode} = 0.34 V - (-0.76 V) = 1.10 V\)
04

Apply the Nernst equation

The Nernst equation relates the cell potential, standard cell potential, temperature, and the concentrations of the species involved in the reaction: \(E_{cell} = E^0_{cell} - \frac{0.05916}{n} \cdot \log{Q}\) where: - \(E_{cell}\) is the cell potential - \(E^0_{cell}\) is the standard cell potential - n is the number of moles of electrons transferred - Q is the reaction quotient For this particular cell, the reaction quotient Q is: \(Q = \frac{[Zn^{2+}]}{[Cu^{2+}]}\) Since [Zn²⁺] has changed by 0.20 mol/L and [Cu²⁺] has changed by the same value but in the opposite direction, we can calculate the new concentrations: \([\mathrm{Zn}^{2+}]_\mathrm{final} \ = \ [\mathrm{Zn}^{2+}]_\mathrm{initial} \ + 0.20 \mathrm{~mol/L} \ = \ 1.00 \mathrm{~mol/L} \ + 0.20 \mathrm{~mol/L} \ = \ 1.20 \mathrm{~mol/L}\) \([\mathrm{Cu}^{2+}]_\mathrm{final} \ = \ [\mathrm{Cu}^{2+}]_\mathrm{initial} \ - 0.20 \mathrm{~mol/L} \ = \ 1.00 \mathrm{~mol/L} \ - 0.20 \mathrm{~mol/L} \ = \ 0.80 \mathrm{~mol/L}\) Now, we can substitute the values into the Nernst equation: \(E_{cell} = 1.10 V - \frac{0.05916}{2} \cdot \log{\frac{1.20}{0.80}}\)
05

Calculate the cell potential

Now we can calculate the cell potential for the new concentrations using the Nernst equation: \(E_{cell} \approx 1.10 V - \frac{0.05916}{2} \cdot \log{1.5}\) \(E_{cell} \approx 1.10 V - 0.02117 V \approx 1.07883 V\) The cell potential after the reaction has operated long enough for the [Zn²⁺] to have changed by 0.20 mol/L is approximately \(1.079 V\).

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Most popular questions from this chapter

When balancing reactions in Chapter 3 , we did not mention that reactions must be charge balanced as well as mass balanced. What do charge balanced and mass balanced mean? How are redox reactions charge balanced?

Consider the cell described below: $$\mathrm{Al}\left|\mathrm{Al}^{3+}(1.00 M)\right|\left|\mathrm{Pb}^{2+}(1.00 M)\right| \mathrm{Pb}$$ Calculate the cell potential after the reaction has operated long enough for the \(\left[\mathrm{Al}^{3+}\right]\) to have changed by \(0.60 \mathrm{~mol} / \mathrm{L}\). (Assume \(\left.T=25^{\circ} \mathrm{C} .\right)\)

A copper penny can be dissolved in nitric acid but not in hydrochloric acid. Using reduction potentials from the book, show why this is so. What are the products of the reaction? Newer pennies contain a mixture of zinc and copper. What happens to the zinc in the penny when the coin is placed in nitric acid? Hydrochloric acid? Support your explanations with data from the book, and include balanced equations for all reactions.

Look up the reduction potential for \(\mathrm{Fe}^{3+}\) to \(\mathrm{Fe}^{2+}\). Look up the reduction potential for \(\mathrm{Fe}^{2+}\) to Fe. Finally, look up the reduction potential for \(\mathrm{Fe}^{3+}\) to Fe. You should notice that adding the reduction potentials for the first two does not give the potential for the third. Why not? Show how you can use the first two potentials to calculate the third potential.

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