Problem 72
Question
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? (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 \(\mathrm{PbSO}_{4} ?\)
Step-by-Step Solution
Verified Answer
The concentration of Pb²⁺ in the anode half-cell is approximately 0.015 M, and the Ksp of PbSO₄ is 0.015.
1Step 1: Identify the two half-reactions
First, let's identify the two half-reactions occurring in the voltaic cell:
1. Cathode (reduction): Sn2+(aq) + 2e- → Sn(s)
2. Anode (oxidation): Pb(s) → Pb2+(aq) + 2e-
2Step 2: Look up the standard reduction potentials
Now, we need to look up the standard reduction potentials for Sn2+(aq) and Pb(s). From standard reduction potential tables, we find:
Eº(Sn2+/Sn) = -0.14 V
Eº(Pb2+/Pb) = -0.13 V
3Step 3: Calculate the overall cell potential
Using the Nernst equation, we can calculate the cell potential:
Ecell = Eº(cell) + \(\frac{RT}{nF}\) * ln(Q)
We know that Ecell is given as +0.22 V. The number of electrons transferred in the reaction, n, is 2. The reaction quotient Q is \(\frac{[Pb^{2+}]}{[Sn^{2+}]}\). We are also given that the concentration of Sn2+ is 1.00 M.
Eº(cell) = Eº(cathode) - Eº(anode) = (-0.14 V) - (-0.13 V) = -0.01 V
Now, we can plug in the values and solve for [Pb2+].
4Step 4: Solve for the concentration of Pb2+
Plugging in the values in the Nernst equation:
0.22 V = -0.01 V + \(\frac{(RT)(2.303)}{2F}\) * log\(\frac{[Pb^{2+}]}{1}\)
0.23 V = \(\frac{(RT)(2.303)}{2F}\) * log([Pb2+])
Now, we can solve for [Pb2+]:
log([Pb2+]) = \(\frac{0.23(2F)}{(2.303)(RT)}\)
[Pb2+] = 10^(\(\frac{0.23(2F)}{(2.303)(RT)}\)) ≈ 0.015 M
5Step 5: Find the Ksp value of PbSO4
Using the information provided in part (b), we know that the concentration of SO42- is 1.00 M in equilibrium with PbSO4(s).
The Ksp expression for PbSO4 is:
Ksp = [Pb2+][SO42-]
Using the concentration of [Pb2+] we found in step 4 and the given [SO42-]:
Ksp = (0.015)(1.00) = 0.015
Therefore, the Ksp of PbSO4 is 0.015.
Key Concepts
Nernst EquationStandard Reduction PotentialsEquilibrium Constant
Nernst Equation
The Nernst equation is a powerful tool in electrochemistry used for determining the cell potential of an electrochemical cell that operates under non-standard conditions. The standard conditions mean reacting concentrations of 1 M, a pressure of 1 atm, and a specified temperature, often 25°C.
The Nernst equation can be written as:
\[ E_{cell} = E^{\circ}_{cell} + \frac{RT}{nF} \ln(Q) \]In this equation:
The Nernst equation can be written as:
\[ E_{cell} = E^{\circ}_{cell} + \frac{RT}{nF} \ln(Q) \]In this equation:
- \(E_{cell}\) is the cell potential at non-standard conditions.
- \(E^{\circ}_{cell}\) is the standard cell potential, indicating the potential difference at standard conditions.
- \(R\) is the universal gas constant (8.314 J/mol K).
- \(T\) is the temperature in Kelvin.
- \(n\) is the number of moles of electrons transferred in the electrochemical reaction.
- \(F\) is the Faraday constant (approximately 96,485 C/mol).
- \(Q\) is the reaction quotient, representing the concentrations or activities of the products and reactants.
Standard Reduction Potentials
Standard reduction potentials are a way to express the tendency of a chemical species to acquire electrons and be reduced. These values are measured in volts and are tabulated for various half-reactions, providing a straightforward way to predict the voltage of galvanic cells.
Every half-cell reaction has a standard reduction potential, \(E^{\circ}\), which is measured under standard conditions. For example:
To find the cell potential, you subtract the potential for the anode (oxidation) from the cathode (reduction):
\[ E^{\circ}_{cell} = E^{\circ}_{cathode} - E^{\circ}_{anode} \]This calculation assists in understanding whether the reaction will proceed spontaneously, which is indicated by a positive cell potential.
Every half-cell reaction has a standard reduction potential, \(E^{\circ}\), which is measured under standard conditions. For example:
- For \( \text{Sn}^{2+} + 2e^- \longrightarrow \text{Sn} \), the standard reduction potential \(E^{\circ} = -0.14 \text{ V}\).
- For \( \text{Pb}^{2+} + 2e^- \longrightarrow \text{Pb} \), \(E^{\circ} = -0.13 \text{ V}\).
To find the cell potential, you subtract the potential for the anode (oxidation) from the cathode (reduction):
\[ E^{\circ}_{cell} = E^{\circ}_{cathode} - E^{\circ}_{anode} \]This calculation assists in understanding whether the reaction will proceed spontaneously, which is indicated by a positive cell potential.
Equilibrium Constant
In complete chemical equilibrium, certain reactions maintain a balance between reactants and products. For solids like salts, this balance is represented by the equilibrium constant, \(K_{sp}\), specifically for sparingly soluble salts.
The expression for \(K_{sp}\) involves the molar concentrations of the constituent ions in a saturated solution. For example, the dissolution of \(\text{PbSO}_4\) can be represented as:
\[ \text{PbSO}_4(s) \leftrightarrow \text{Pb}^{2+}(aq) + \text{SO}_4^{2-}(aq) \]The corresponding solubility product expression would be:
\[ K_{sp} = [\text{Pb}^{2+}][\text{SO}_4^{2-}] \]In this expression, each term represents the concentration of that ion at equilibrium.
For the reaction given in the exercise, we calculated \([\text{Pb}^{2+}]\) to be 0.015 M and with \([\text{SO}_4^{2-}] = 1.00 \text{ M}\), the \(K_{sp}\) can be determined as:
\[ K_{sp} = (0.015)(1.00) = 0.015 \]This value provides crucial insights into the solubility and stability of salts in aqueous solutions.
The expression for \(K_{sp}\) involves the molar concentrations of the constituent ions in a saturated solution. For example, the dissolution of \(\text{PbSO}_4\) can be represented as:
\[ \text{PbSO}_4(s) \leftrightarrow \text{Pb}^{2+}(aq) + \text{SO}_4^{2-}(aq) \]The corresponding solubility product expression would be:
\[ K_{sp} = [\text{Pb}^{2+}][\text{SO}_4^{2-}] \]In this expression, each term represents the concentration of that ion at equilibrium.
For the reaction given in the exercise, we calculated \([\text{Pb}^{2+}]\) to be 0.015 M and with \([\text{SO}_4^{2-}] = 1.00 \text{ M}\), the \(K_{sp}\) can be determined as:
\[ K_{sp} = (0.015)(1.00) = 0.015 \]This value provides crucial insights into the solubility and stability of salts in aqueous solutions.
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