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A \(1 M\) solution of \(\mathrm{Cu}\left(\mathrm{NO}_{3}\right)_{2}\) is placed in a beaker with a strip of Cu metal. A \(1 M\) solution of \(\mathrm{SnSO}_{4}\) is placed in a second beaker with a strip of Sn metal. A salt bridge connects the two beakers, and wires to a voltmeter link the two metal electrodes. (a) Which electrode serves as the anode, and which as the cathode? (b) Which electrode gains mass and which loses mass as the cell reaction proceeds? (c) Write the equation for the overall cell reaction. (d) What is the emf generated by the cell under standard conditions?

Short Answer

Expert verified
The anode is the Sn electrode and the cathode is the Cu electrode. The Sn electrode loses mass, while the Cu electrode gains mass. The overall cell reaction is Sn(s) + Cu²⁺ → Sn²⁺ + Cu(s), and the emf generated under standard conditions is \( +0.48 V \).

Step by step solution

01

Determine the anode and cathode

In our cell, we have two half-cells. The first half-cell contains a solution of Cu(NO₃)₂ and Cu metal, while the second half-cell has a solution of SnSO₄ and Sn metal. To identify which electrode serves as the anode and which as the cathode, we will look at the standard electrode potentials of the two half-cells. For Cu²⁺ + 2e⁻ → Cu(s), the standard reduction potential E° is \( +0.34 V \) For Sn²⁺ + 2e⁻ → Sn(s), the standard reduction potential E° is \( -0.14 V \) Since the half-cell with a lower reduction potential will be oxidized (lose electrons) and serve as the anode, in this case, it's Sn(s) → Sn²⁺ + 2e⁻, and the anode is the Sn electrode. The Cu electrode will be the cathode.
02

Identify the electrode gaining and losing mass

The anode loses mass because the solid metal is oxidized and enters the solution. In our cell, the Sn metal loses mass because it undergoes the reaction: Sn(s) → Sn²⁺ + 2e⁻. At the cathode, Cu²⁺ ions in the solution gain electrons and are reduced to form solid Cu metal, causing the Cu electrode to gain mass. The reaction occurring at the cathode is: Cu²⁺ + 2e⁻ → Cu(s).
03

Write the overall cell reaction

To obtain the overall cell reaction, we will combine the oxidation and reduction half-cell reactions. Keep in mind that electrons should cancel out in the final cell reaction. Anode (oxidation): Sn(s) → Sn²⁺ + 2e⁻ Cathode (reduction): Cu²⁺ + 2e⁻ → Cu(s) Overall cell reaction: Sn(s) + Cu²⁺ → Sn²⁺ + Cu(s)
04

Calculate the emf generated by the cell under standard conditions

To calculate the emf generated by the cell under standard conditions, we can use the Nernst Equation for standard conditions: E°(cell) = E°(cathode) - E°(anode) We already know the standard reduction potentials for both half-cells: E°(Cu²⁺/Cu) = \( +0.34 V \) E°(Sn²⁺/Sn) = \( -0.14 V \) Now, we can input these values into the Nernst Equation: E°(cell) = (+0.34 V) - (-0.14 V) = +0.48 V The emf generated by the cell under standard conditions is \( +0.48 V \).

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Key Concepts

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

Redox Reactions
Redox reactions are fundamental to the functioning of electrochemical cells. In these reactions, one element is oxidized, while another is reduced. Oxidation refers to the loss of electrons, and reduction refers to the gain of electrons. A mnemonic to remember this is "OIL RIG": Oxidation Is Loss, Reduction Is Gain. In the given exercise, the redox reaction occurs between tin (Sn) and copper (Cu). While the tin loses electrons becoming oxidized to form Sn²⁺ ions, the copper ions gain electrons and are thus reduced to become solid copper metal. Understanding these electron transfers is key to figuring out how a galvanic cell functions.
Standard Electrode Potentials
Standard electrode potentials are values that indicate how readily a species gains electrons (is reduced) under standard conditions (1 M concentration, 1 atm pressure, and 25°C). They are measured in volts (V) and serve as a comparative tool to predict the direction of flow of electrons in a redox reaction. Every half-reaction has a standard electrode potential associated with it:
  • For the reduction of Cu²⁺ to Cu, the potential is +0.34 V.
  • For the reduction of Sn²⁺ to Sn, the potential is -0.14 V.
A more positive standard electrode potential means a greater tendency to be reduced. In our exercise, since Cu has a more positive value compared to Sn, it acts as the cathode, undergoing reduction, while Sn serves as the anode, undergoing oxidation.
Galvanic Cells
A galvanic cell, also known as a voltaic cell, is a device that converts chemical energy into electrical energy through a spontaneous redox reaction. It consists of two half-cells connected by a salt bridge, which facilitates the movement of ions and maintains electrical neutrality. In the exercise example, one half-cell has a copper electrode in a Cu(NO₃)₂ solution, and the other a tin electrode in a SnSO₄ solution.
  • The anode is the Sn electrode, where oxidation occurs, resulting in a loss of mass as Sn atoms transform into Sn²⁺ ions.
  • The cathode is the Cu electrode, where reduction occurs, gaining mass as Cu²⁺ ions turn into solid Cu.
These reactions generate an electric current, which can be captured for external work or measured using a voltmeter.
Nernst Equation
The Nernst Equation is a powerful tool in electrochemistry that calculates the electromotive force (emf) of a cell under non-standard conditions. However, when conditions are standard, the equation simplifies to this:\[ E^°(cell) = E^°(cathode) - E^°(anode) \]In the exercise scenario, it's underlined that the cell operates under standard conditions, making this equation particularly straightforward to use. By substituting the given standard potentials:
  • For the cathode (Cu): +0.34 V
  • For the anode (Sn): -0.14 V
You plug in these values to get the emf of:\[ E^°(cell) = (+0.34 \, V) - (-0.14 \, V) = +0.48 \, V \]This positive value firmly indicates that the cell reaction is spontaneous and capable of generating electrical energy effectively.

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Most popular questions from this chapter

(a) Why is it impossible to measure the standard reduction potential of a single half-reaction? (b) Describe how the standard reduction potential of a half-reaction can be determined.

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

A voltaic cell similar to that shown in Figure \(20.5\) is constructed. One electrode compartment consists of a silver strip placed in a solution of \(\mathrm{AgNO}_{3}\), and the other has an iron strip placed in a solution of \(\mathrm{FeCl}_{2}\). The overall cell reaction is $$ \mathrm{Fe}(s)+2 \mathrm{Ag}^{+}(a q) \longrightarrow \mathrm{Fe}^{2+}(a q)+2 \mathrm{Ag}(s) $$ (a) What is being oxidized, and what is being reduced? (b) Write the half-reactions that occur in the two electrode compartments. (c) Which electrode is the anode, and which is the cathode? (d) Indicate the signs of the electrodes. (e) Do electrons flow from the silver electrode to the iron electrode, or from the iron to the silver? (f) In which directions do the cations and anions migrate through the solution?

A voltaic cell is constructed with two \(\mathrm{Zn}^{2+}-\mathrm{Zn}\) electrodes. The two cell compartments have \(\left[\mathrm{Zn}^{2+}\right]=1.8 \mathrm{M}\) and \(\left[\mathrm{Zn}^{2+}\right]=1.00 \times 10^{-2} M\), respectively. (a) Which electrode is the anode of the cell? (b) What is the standard emf of the cell? (c) What is the cell emf for the concentrations given? (d) For each electrode, predict whether \(\left[\mathrm{Zn}^{2+}\right]\) will increase, decrease, or stay the same as the cell operates.

Complete and balance the following equations, and identify the oxidizing and reducing agents. Recall that the \(\mathrm{O}\) atoms in hydrogen peroxide, \(\mathrm{H}_{2} \mathrm{O}_{2}\), have an atypical oxidation state. (a) \(\mathrm{NO}_{2}^{-}(a q)+\mathrm{Cr}_{2} \mathrm{O}_{7}^{2-}(a q)-\cdots\) \(\mathrm{Cr}^{3+}(a q)+\mathrm{NO}_{3}^{-}(a q)\) (acidic solution) (b) \(\mathrm{S}(s)+\mathrm{HNO}_{3}(a q) \rightarrow-\rightarrow \mathrm{H}_{2} \mathrm{SO}_{3}(a q)+\mathrm{N}_{2} \mathrm{O}(g)\) (acidic solution) (c) \(\mathrm{Cr}_{2} \mathrm{O}_{7}^{2-}(a q)+\mathrm{CH}_{3} \mathrm{OH}(a q) \longrightarrow\) \(\mathrm{HCO}_{2} \mathrm{H}(a q)+\mathrm{Cr}^{3+}(a q)\) (acidic solution) (d) \(\mathrm{MnO}_{4}^{-}(a q)+\mathrm{Cl}^{-}(a q) \longrightarrow \mathrm{Mn}^{2+}(a q)+\mathrm{Cl}_{2}(a q)\) (acidic solution) (e) \(\mathrm{NO}_{2}^{-}(a q)+\mathrm{Al}(s) \longrightarrow \mathrm{NH}_{4}{ }^{+}(a q)+\mathrm{AlO}_{2}^{-}(a q)\) (basic solution) (f) \(\mathrm{H}_{2} \mathrm{O}_{2}(a q)+\mathrm{ClO}_{2}(a q) \longrightarrow \mathrm{ClO}_{2}^{-}(a q)+\mathrm{O}_{2}(g)\) (basic solution)

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