Warning: foreach() argument must be of type array|object, bool given in /var/www/html/web/app/themes/studypress-core-theme/template-parts/header/mobile-offcanvas.php on line 20

A voltaic cell is constructed that is based on the following reaction: $$ \mathrm{Sn}^{2+}(a q)+\mathrm{Pb}(s) \longrightarrow \mathrm{Sn}(s)+\mathrm{Pb}^{2+}(a q) $$ (a) If the concentration of \(\mathrm{Sn}^{2+}\) in the cathode half-cell is \(1.00 M\) and the cell generates an emf of \(+0.22 \mathrm{~V},\) what is the concentration of \(\mathrm{Pb}^{2+}\) in the anode half-cell? \((\mathbf{b})\) If the anode half-cell contains \(\left[\mathrm{SO}_{4}^{2-}\right]=1.00 M\) in equilibrium with \(\mathrm{PbSO}_{4}(s),\) what is the \(K_{s p}\) of \(\mathrm{PbSO}_{4} ?\)

Short Answer

Expert verified
In short, the concentration of \(\mathrm{Pb}^{2+}\) in the anode half-cell is \(6.0\times10^{7}\,\mathrm{M}\), and the solubility product constant (\(K_{sp}\)) for \(\mathrm{PbSO}_{4}\) is \(6.0\times10^{7}\).

Step by step solution

01

Write the Nernst equation

The Nernst equation relates the concentration of the species involved in the reaction to the cell potential (emf): \(E_{cell} = E_{cell}^{0} - \dfrac{0.0592}{n} \log_{10}{\dfrac{[\mathrm{Pb}^{2+}]}{[\mathrm{Sn}^{2+}]}}\) We need to substitute the given values and calculate \([\mathrm{Pb}^{2+}]\), i.e., the concentration of \(\mathrm{Pb}^{2+}\) in the anode half-cell.
02

Substitute the given values into the Nernst equation

We have: \(E_{cell}= +0.22\,\mathrm{V}\), \([\mathrm{Sn}^{2+}] = 1.00 \,\mathrm{M}\). The standard cell potential, \(E_{cell}^{0}\), can be found from the standard reduction potentials of \(\mathrm{Sn}^{2+}\) and \(\mathrm{Pb}^{2+}\). Since both ions have a +2 charge, \(n=2\). For the reaction \(\mathrm{Sn}^{2+} + 2e^{-} \longrightarrow \mathrm{Sn}(s)\), the standard reduction potential is \(E^{0}(\mathrm{Sn}) = -0.14\,\mathrm{V}\). For the reaction \(\mathrm{Pb}^{2+} + 2e^{-} \longrightarrow \mathrm{Pb}(s)\), the standard reduction potential is \(E^{0}(\mathrm{Pb}) = -0.13\,\mathrm{V}\). The standard cell potential can be determined as: \(E_{cell}^{0}= E^{0}(\mathrm{Sn}) - E^{0}(\mathrm{Pb}) = -0.14-(-0.13)= -0.01\,\mathrm{V}\). Now, substitute these values into the Nernst equation: \(0.22 = -0.01 - \dfrac{0.0592}{2} \log_{10}{\dfrac{[\mathrm{Pb}^{2+}]}{1}}\)
03

Solve for the concentration of \(\mathrm{Pb}^{2+}\)

Now, we can solve for \([\mathrm{Pb}^{2+}]\): \(0.23= \dfrac{0.0592}{2} \log_{10}{[\mathrm{Pb}^{2+}]}\) \(7.776=\log_{10}{[\mathrm{Pb}^{2+}]}\) \(10^{7.776}=[\mathrm{Pb}^{2+}]\) Therefore, \([\mathrm{Pb}^{2+}]=6.0\)x\(10^{7}\,\mathrm{M}\).
04

Write the expression for the equilibrium constant, \(K_{sp}\)

The reaction for \(\mathrm{PbSO}_{4}(s)\) dissolution is: \(\mathrm{PbSO}_{4}(s) \longleftrightarrow \mathrm{Pb}^{2+}(a q) + \mathrm{SO}_{4}^{2-}(a q)\) Now we can write the expression for the solubility product constant, \(K_{sp}\): \(K_{sp} = [\mathrm{Pb}^{2+}][\mathrm{SO}_{4}^{2-}]\)
05

Substitute the values and find \(K_{sp}\)

We have: \([\mathrm{Pb}^{2+}] = 6.0\)x\(10^{7}\,\mathrm{M}\) and \([\mathrm{SO}_{4}^{2-}] = 1.00\,\mathrm{M}\). Now, plug in the values in the expression for \(K_{sp}\): \(K_{sp} = (6.0\times10^{7})(1.00)\) Hence, \(K_{sp} = 6.0\)x\(10^{7}\).

Unlock Step-by-Step Solutions & Ace Your Exams!

  • Full Textbook Solutions

    Get detailed explanations and key concepts

  • Unlimited Al creation

    Al flashcards, explanations, exams and more...

  • Ads-free access

    To over 500 millions flashcards

  • Money-back guarantee

    We refund you if you fail your exam.

Over 30 million students worldwide already upgrade their learning with Vaia!

Key Concepts

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

Nernst Equation
The Nernst equation is a crucial tool in electrochemistry, especially when dealing with voltaic or galvanic cells. It connects the potential of an electrochemical cell to the concentrations of the reacting ions. Understanding this equation allows us to predict how changes in concentration affect the electromotive force (emf) of the cell.

The Nernst equation is written as:
  • \( E_{cell} = E_{cell}^{0} - \frac{0.0592}{n} \log_{10}{\frac{[\mathrm{Pb}^{2+}]}{[\mathrm{Sn}^{2+}]}} \)
Here, \( E_{cell} \) is the actual cell potential and \( E_{cell}^{0} \) is the standard cell potential. The number \( n \) is the number of electrons transferred in the reaction. The concentrations are in molar units.

In our case, knowing the emf is \(+0.22 \, \mathrm{V}\) and the concentrations allow us to rearrange this equation and solve for unknown values like the \([\mathrm{Pb}^{2+}]\). This equation is essential for predicting cell behavior under non-standard conditions.
Standard Reduction Potential
Standard reduction potentials measure the tendency of a chemical species to gain electrons and be reduced. These potentials are determined under standard conditions (1 M concentration, 1 atm pressure, and 25°C), and they play a pivotal role in understanding which way a redox reaction will proceed.

In a voltaic cell, reactions occur in two half-cells, each with its own standard reduction potential. The equation for the cell potential is:
  • \( E_{cell}^{0} = E_{reduction}^{0} - E_{oxidation}^{0} \)
In the provided exercise, the standard reduction potential for the reaction of \(\mathrm{Sn}^{2+}\) to \(\mathrm{Sn}(s)\) is \(-0.14\, \mathrm{V}\), while that for \(\mathrm{Pb}^{2+}\) to \(\mathrm{Pb}(s)\) is \(-0.13\, \mathrm{V}\). The negative reduction potential indicates that these are less likely to occur spontaneously, meaning they favor oxidation.

The difference between these potentials lets us calculate the standard cell potential, \(E_{cell}^{0}\), which is often used in the Nernst equation.
Solubility Product Constant
The solubility product constant, known as \(K_{sp}\), is an equilibrium constant for the dissolution of a sparingly soluble compound. It provides insight into the solubility of ionic compounds and helps predict precipitation reactions.

The dissolution reaction for \(\mathrm{PbSO}_{4}(s)\) is:
  • \( \mathrm{PbSO}_{4}(s) \leftrightarrow \mathrm{Pb}^{2+}(aq) + \mathrm{SO}_{4}^{2-}(aq) \)
Therefore, the \(K_{sp}\) expression is:
  • \( K_{sp} = [\mathrm{Pb}^{2+}]\times[\mathrm{SO}_{4}^{2-}] \)
Understanding and calculating \(K_{sp}\) is crucial for predicting whether a salt will dissolve or precipitate in solution. In the exercise, we use calculated concentrations from the Nernst equation to determine \(K_{sp}\) for \(\mathrm{PbSO}_{4}\), demonstrating the interconnectedness of electrochemical and solubility concepts.

One App. One Place for Learning.

All the tools & learning materials you need for study success - in one app.

Get started for free

Most popular questions from this chapter

A voltaic cell is constructed that uses the following half-cell reactions: $$ \begin{array}{l} \mathrm{Ag}^{+}(a q)+2 \mathrm{e}^{-} \longrightarrow \mathrm{Ag}(s) \\ \mathrm{I}_{2}(s)+2 \mathrm{e}^{-} \longrightarrow 2 \mathrm{I}^{-}(a q) \end{array} $$ The cell is operated at \(298 \mathrm{~K}\) with \(\left[\mathrm{Ag}^{+}\right]=0.15 \mathrm{M}\) and \(\left[\mathrm{I}^{-}\right]=0.035 \mathrm{M}\). (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) With \(\left[\mathrm{Ag}^{+}\right]\) equal to \(0.15 \mathrm{M}\), at what concentration of \(\mathrm{I}^{-}\) would the cell have zero potential?

(a) Suppose that an alkaline battery was manufactured using cadmium metal rather than zinc. What effect would this have on the cell emf? (b) What environmental advantage is provided by the use of nickel-metal hydride batteries over nickel-cadmium batteries?

Mercuric oxide dry-cell batteries are often used where a flat discharge voltage and long life are required, such as in watches and cameras. The two half-cell reactions that occur in the battery are $$ \begin{array}{l} \mathrm{HgO}(s)+\mathrm{H}_{2} \mathrm{O}(l)+2 \mathrm{e}^{-} \longrightarrow \mathrm{Hg}(l)+2 \mathrm{OH}^{-}(a q) \\ \mathrm{Zn}(s)+2 \mathrm{OH}^{-}(a q) \longrightarrow \mathrm{ZnO}(s)+\mathrm{H}_{2} \mathrm{O}(l)+2 \mathrm{e}^{-} \end{array} $$ (a) Write the overall cell reaction. (b) The value of \(E_{\text {red }}^{\circ}\) for the cathode reaction is \(+0.098 \mathrm{~V}\). The overall cell potential is \(+1.35 \mathrm{~V}\). Assuming that both half-cells operate under standard conditions, what is the standard reduction potential for the anode reaction? (c) Why is the potential of the anode reaction different than would be expected if the reaction occurred in an acidic medium?

(a) What is an electrolytic cell? (b) The negative terminal of a voltage source is connected to an electrode of an electrolytic cell. Is the electrode the anode or the cathode of the cell? Explain. (c) The electrolysis of water is often done with a small amount of sulfuric acid added to the water. What is the role of the sulfuric acid? (d) Why are active metals such as Al obtained by electrolysis using molten salts rather than aqueous solutions?

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 \(\left[\mathrm{Zn}^{2+}\right]=0.100 \mathrm{M} ?(\mathbf{c})\) What is the emf of the cell when \(\left[\mathrm{Ni}^{2+}\right]=0.200 M\) and \(\left[\mathrm{Zn}^{2+}\right]=0.900 \mathrm{M} ?\)

See all solutions

Recommended explanations on Chemistry Textbooks

View all explanations

What do you think about this solution?

We value your feedback to improve our textbook solutions.

Study anywhere. Anytime. Across all devices.

Sign-up for free