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Using standard reduction potentials (Appendix E), calculate the standard emf for each of the following reactions: (a) \(\mathrm{C}_{2}(\mathrm{~g})+2 \mathrm{I}^{\mathrm{a}}(\mathrm{aq}) \longrightarrow 2 \mathrm{Cl}^{-}(a q)+\mathrm{I}_{2}(s)\) (b) \(\mathrm{Ni}(s)+2 \mathrm{Ce}^{4+}(a q) \longrightarrow \mathrm{Ni}^{2+}(a q)+2 \mathrm{Ce}^{3+}(a q)\) (c) \(\mathrm{Fe}(s)+2 \mathrm{Fe}^{3+}(a q) \longrightarrow 3 \mathrm{Fe}^{2+}(a q)\) (d) \(2 \mathrm{NO}_{3}^{-}(a q)+8 \mathrm{H}^{+}(a q)+3 \mathrm{Cu}(s) \longrightarrow 2 \mathrm{NO}(g)+\) \(4 \mathrm{H}_{2} \mathrm{O}(I)+3 \mathrm{Cu}^{2+}(a q)\)

Short Answer

Expert verified
Short Answer: The standard emfs for the given reactions are: (a) \(E_{cell} = 0.82\,\mathrm{V}\) (b) \(E_{cell} = 1.86\,\mathrm{V}\) (c) \(E_{cell} = 1.21\,\mathrm{V}\) (d) \(E_{cell} = -0.63\,\mathrm{V}\)

Step by step solution

01

Identify the half-reactions

Write the half-reactions. 1. Oxidation half-reaction: \(2I^{-}(aq) \longrightarrow I_{2}(s) + 2e^{-}\) 2. Reduction half-reaction: \(Cl_{2}(g) + 2e^{-} \longrightarrow 2Cl^{-}(aq)\)
02

Look up the standard reduction potentials

Find the standard reduction potentials for both half-reactions. According to Appendix E: 1. \(I_{2}(s) + 2e^{-} \longrightarrow 2I^{-}(aq)\) : \(E^\circ_{red,I} = 0.54\,\mathrm{V}\) 2. \(Cl_{2}(g) + 2e^{-} \longrightarrow 2Cl^{-}(aq)\) : \(E^\circ_{red,Cl} = 1.36\,\mathrm{V}\)
03

Calculate the standard emf

Use the given equation: \(E_{cell} = E_{cathode} - E_{anode} = E^\circ_{red,Cl} - E^\circ_{red,I} = 1.36\,\mathrm{V} - 0.54\,\mathrm{V} = 0.82\,\mathrm{V}\) (b) \(Ni^{2+}(aq) + 2e^{-} \longrightarrow Ni(s)\) \(2Ce^{3+}(aq) + 2e^{-} \longrightarrow 2Ce^{4+}(aq)\)
04

Identify the half-reactions

Write the half-reactions. 1. Oxidation half-reaction: \(Ni(s) \longrightarrow Ni^{2+}(aq) + 2e^{-}\) 2. Reduction half-reaction: \(2Ce^{4+}(aq) + 2e^{-} \longrightarrow 2Ce^{3+}(aq)\)
05

Look up the standard reduction potentials

Find the standard reduction potentials for both half-reactions. According to Appendix E: 1. \(Ni^{2+}(aq) + 2e^{-} \longrightarrow Ni(s)\) : \(E^\circ_{red,Ni} = -0.25\,\mathrm{V}\) 2. \(Ce^{4+}(aq) + e^{-} \longrightarrow Ce^{3+}(aq)\) : \(E^\circ_{red,Ce} = 1.61\,\mathrm{V}\)
06

Calculate the standard emf

Use the given equation: \(E_{cell} = E_{cathode} - E_{anode} = E^\circ_{red,Ce} - E^\circ_{red,Ni} = 1.61\,\mathrm{V} - (-0.25\,\mathrm{V}) = 1.86\,\mathrm{V}\) (c) \(Fe^{2+}(aq) + 2e^{-} \longrightarrow Fe(s)\) \(Fe^{3+}(aq) + e^{-} \longrightarrow Fe^{2+}(aq)\)
07

Identify the half-reactions

Write the half-reactions. 1. Oxidation half-reaction: \(Fe(s) \longrightarrow Fe^{2+}(aq) + 2e^{-}\) 2. Reduction half-reaction: \(2Fe^{3+}(aq) + 2e^{-} \longrightarrow 2Fe^{2+}(aq)\)
08

Look up the standard reduction potentials

Find the standard reduction potentials for both half-reactions. According to Appendix E: 1. \(Fe^{2+}(aq) + 2e^{-} \longrightarrow Fe(s)\) : \(E^\circ_{red,Fe2} = -0.44\,\mathrm{V}\) 2. \(Fe^{3+}(aq) + e^{-} \longrightarrow Fe^{2+}(aq)\) : \(E^\circ_{red,Fe3} = 0.77\,\mathrm{V}\)
09

Calculate the standard emf

Use the given equation: \(E_{cell} = E_{cathode} - E_{anode} = E^\circ_{red,Fe3} - E^\circ_{red,Fe2} = 0.77\,\mathrm{V} - (-0.44\,\mathrm{V}) = 1.21\,\mathrm{V}\) For reaction (d), we will need to split it into three half-reactions due to the presence of multiple elements changing oxidation states. (d) \(NO_{3}^{-}(aq) + 2H^{+}(aq) + e^{-} \longrightarrow NO(g) + H_{2}O(l)\) \(2H^{+}(aq) + 2e^{-} \longrightarrow H_{2}(g)\) \(Cu^{2+}(aq) + 2e^{-} \longrightarrow Cu(s)\)
10

Identify the half-reactions

Write the half-reactions. 1. Oxidation half-reaction: \(2NO(g) + H_{2}O(l) \longrightarrow 2NO_{3}^{-}(aq) + 2H^{+}(aq) + 2e^{-}\) 2. Reduction half-reaction: \(2H^{+}(aq) + 2e^{-} \longrightarrow H_{2}(g)\) 3. Reduction half-reaction: \(3Cu(s) \longrightarrow 3Cu^{2+}(aq) + 6e^{-}\)
11

Balance the electrons in the half-reactions

Before looking up the standard reduction potentials, balance the electrons in the half-reactions. 1. The NO half-reaction releases 2 electrons. 2. The H_{2} half-reaction consumes 2 electrons. 3. The Cu half-reaction consumes 6 electrons. The net release of electrons from the oxidation half-reaction should equal the net consumption of electrons by the reduction half-reactions. Therefore, multiply the Cu half-reaction by 2/3 to make it consume 4 electrons: \(2Cu(s) \longrightarrow 2Cu^{2+}(aq) + 4e^{-}\)
12

Look up the standard reduction potentials

Find the standard reduction potentials for all balanced half-reactions. According to Appendix E: 1. \(NO_{3}^{-}(aq) + 2H^{+}(aq) + e^{-} \longrightarrow NO(g) + H_{2}O(l)\) : \(E^\circ_{red,NO} = 0.97\,\mathrm{V}\) 2. \(2H^{+}(aq) + 2e^{-} \longrightarrow H_{2}(g)\) : \(E^\circ_{red,H} = 0\,\mathrm{V}\) 3. \(Cu^{2+}(aq) + 2e^{-} \longrightarrow Cu(s)\) : \(E^\circ_{red,Cu} = 0.34\,\mathrm{V}\)
13

Calculate the standard emf

Use the given equation: \(E_{cell} = E_{cathode1} - E_{anode} + E_{cathode2} = E^\circ_{red,H} - E^\circ_{red,NO} + E^\circ_{red,Cu} = 0\,\mathrm{V} - 0.97\,\mathrm{V} + 0.34\,\mathrm{V} = -0.63\,\mathrm{V}\)

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Standard Reduction Potentials
Standard reduction potentials are critical in electrochemistry. They represent the tendency of a chemical species to acquire electrons and be reduced. These potentials are measured under standard conditions: 25°C, 1 atm pressure, and 1 M concentration for all aqueous species. In electrochemical reactions, such potentials are listed as reduction potentials and are used to predict the direction of redox reactions.

Each half-reaction has its own standard reduction potential, denoted as \(E^0_{red}\). For instance, in the exercise, the reduction half-reaction of \(Cl_2(g)\) converting into \(2Cl^-(aq)\) has a reduction potential \(E^0_{red,Cl} = 1.36\,\mathrm{V}\).

Higher positive values indicate a greater likelihood of a substance being reduced, as seen in the comparison of \(Cl_2\) and \(I_2\), where chlorine is more readily reduced.
Electromotive Force Calculation
Electromotive force (emf) is the driving force behind the flow of electrons in an electrochemical cell. To calculate the standard emf \(E_{cell}\) for a given reaction, we utilize standard reduction potentials. The formula is quite straightforward:

\[ E_{cell} = E_{cathode} - E_{anode} \]

In the context of a redox reaction, the cathode is the site of reduction, while the anode is the site of oxidation. Using the standard reduction potentials from the example, where \(E_{cathode}\) for chloride is 1.36 V and \(E_{anode}\) for iodide is 0.54 V, the emf is calculated as:

\[ E_{cell} = 1.36\,\mathrm{V} - 0.54\,\mathrm{V} = 0.82\,\mathrm{V} \]

This positive result indicates a spontaneous reaction under standard conditions.
Oxidation and Reduction Half-Reactions
Understanding half-reactions is essential for grasping redox processes. A reaction consists of two parts: oxidation, where a substance loses electrons, and reduction, where a substance gains electrons. These are better understood as half-reactions.

In the provided exercise, the reaction \(2I^-(aq)\) oxidizing to \(I_2(s)\) represents the oxidation half-reaction, while \(Cl_2(g)\) reducing to \(2Cl^-(aq)\) is the reduction half-reaction. Oxidation involves electron loss, and that is why the \(I^-\) species loses electrons to form \(I_2\).

Always identify the species undergoing oxidation and reduction separately to analyze redox reactions correctly. This separation allows for the correct application of the Nernst equation or other electrochemical principles.
Balancing Redox Reactions
Balancing redox reactions ensures the conservation of mass and charge, crucial in achieving accurate chemical equations. It involves a methodical approach:

  • Separate the reaction into its oxidation and reduction half-reactions.
  • Balance the number of atoms other than hydrogen and oxygen.
  • Balance oxygen atoms by adding \(H_2O\).
  • Balance hydrogen atoms by adding \(H^+\).
  • Balance the charge by adding electrons.
  • Finally, equalize the electron transfer between the half-reactions.

This process was evident when adjusting the copper reaction in the given exercise. By balancing the electrons lost and gained, reactants and products appeared in correct proportions, aligning with laws of conservation. Accurate balancing allows correct emf calculations, ensuring predictive reactions in galvanic or voltaic cells.

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Most popular questions from this chapter

During a period of discharge of a lead-acid battery, \(402 \mathrm{~g}\) of \(\mathrm{Pb}\) from the anode is converted into \(\mathrm{PbSO}_{4}(s)\). (a) What mass of \(\mathrm{PbO}_{2}(s)\) is reduced at the cathode during this same period? (b) How many coulombs of electrical charge are transferred from \(\mathrm{Pb}\) to \(\mathrm{PbO}_{2}\) ?

In some applications nickel-cadmium batteries have been replaced by nickel- zine batteries. The overall cell reaction for this relatively new battery is: $$ \begin{aligned} 2 \mathrm{H}_{2} \mathrm{O}(l)+2 \mathrm{NiO}(\mathrm{OH})(s)+\mathrm{Zn}(s) \\\ \longrightarrow 2 \mathrm{Ni}(\mathrm{OH})_{2}(s)+\mathrm{Zn}(\mathrm{OH})_{2}(s) \end{aligned} $$ (a)What is the cathode half-reaction? (b) What is the anode half-reaction? (c) A single nickel-cadmium cell has a voltage of \(1.30 \mathrm{~V}\). Based on the difference in the standard reduction potentials of \(\mathrm{Cd}^{2+}\) and \(\mathrm{Zn}^{2+}\), what voltage would you estimate a nickel-zinc battery will produce? (d) Would you expect the specific energy density of a nickel-zinc battery to be higher or lower than that of a nickel-cadmium battery?

For a spontaneous reaction \(\mathrm{A}(a q)+\mathrm{B}(a q) \longrightarrow \mathrm{A}^{-}(a q)+\) \(\mathrm{B}^{+}(\mathrm{at})\), answer the following questions: (a) If you made a voltaic cell out of this reaction, what halfreaction would be occurring at the cathode, and what halfreaction would be occurring at the anode? (b) Which half-reaction from (a) is higher in potential energy? (c) What is the sign of \(E_{\text {cell? }}^{\text {? }}\) [Section 20.3]

A common shorthand way to represent a voltaic cell is anode | anode solution || cathode solution |cathode A double vertical line represents a salt bridge or a porous barrier. A single vertical line represents a change in phase, such AS from solid to solution. (a) Write the half-reactions and overall cell reaction represented by Fe \(\left|\mathrm{Fe}^{2+}\right|\left|\mathrm{Ag}^{+}\right| \mathrm{Ag}_{\mathrm{g}}\) sketch the cell. (b) Write the half-reactions and overall cell reaction represented by \(\mathrm{Zn}\left|\mathrm{Zn}^{2+}\right|\left|\mathrm{H}^{+}\right| \mathrm{H}_{3}\) s sketch the cell. (c) Using the notation just described, represent a cell based on the following reaction: $$ \begin{aligned} \mathrm{ClO}_{3}^{-}(a q)+3 \mathrm{Cu}(s)+6 \mathrm{H}^{+}(a q) & \longrightarrow \mathrm{Cl}^{-}(a q)+3 \mathrm{Cu}^{2+}(a q)+3 \mathrm{H}_{2} \mathrm{O}(l) \end{aligned} $$ Pt is used as an inert electrode in contact with the \(\mathrm{ClO}_{3}^{-}\)and Cl. Sketch the cell.

A voltaic cell is based on \(\mathrm{Ag}^{+}(a q) / \mathrm{Ag}(s)\) and \(\mathrm{Fe}^{3+}(a q) /\) \(\mathrm{Fe}^{2+}(\mathrm{aq})\) half-cells. (a) What is the standard emf of the cell? (b) Which reaction occurs at the cathode and which at the anode of the cell? (c) Use \(S^{\circ}\) values in Appendix \(\mathrm{C}\) and the relationship between cell potential and free-energy change to predict whether the standard cell potential increases or decreases when the temperature is raised above \(25^{\circ} \mathrm{C}\).

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