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What is \(E^{\circ}\) at \(25^{\circ} \mathrm{C}\) for the following reaction? $$ \begin{array}{c} \mathrm{Ba}^{2+}(a q)+\mathrm{SO}_{4}^{2-}(a q) \longrightarrow \mathrm{BaSO}_{4}(s) \\ K_{\mathrm{sp}} \text { for } \mathrm{BaSO}_{4} \text { is } 1.1 \times 10^{-10} \end{array} $$

Short Answer

Expert verified
Answer: The standard reduction potential (E°) cannot be determined for the given precipitation reaction, as it requires information from a redox reaction, which is not available in this case.

Step by step solution

01

Write down the Nernst equation

The Nernst equation relates the reduction potential of a redox reaction to the standard reduction potential, temperature, and concentrations of the species involved: $$ E = E^\circ - \frac{RT}{nF} \ln Q $$ where, E = Reduction potential of the reaction E° = Standard reduction potential R = Gas constant (8.314 J/mol·K) T = Temperature in Kelvin (25°C = 298.15 K) n = Number of electrons transferred in the reaction F = Faraday's constant (96,485 C/mol) Q = Reaction quotient
02

Determine the number of electrons transferred (n)

Since there is no redox reaction taking place in the equation, we can assume that the value of n is 1. This simplifies the Nernst equation.
03

Calculate the Reaction Quotient (Q) using Ksp

The reaction quotient (Q) for the given reaction can be expressed as: $$ Q = [\mathrm{Ba^{2+}}][\mathrm{SO_4^{2-}}] $$ As the solubility product constant for BaSO₄ is given, we can write: $$ K_{sp} = [\mathrm{Ba^{2+}}][\mathrm{SO_4^{2-}}] $$ So, the reaction quotient Q is equal to the solubility product constant Ksp: $$ Q = 1.1 × 10^{-10} $$
04

Substitute the values and solve for E°

Now we can substitute the values for T, n, F, and Q in the Nernst equation and solve for the standard reduction potential E°: $$ E = E^\circ - \frac{8.314\,\mathrm{J/mol\cdot K} \times 298.15\,\mathrm{K}}{1 \times 96,485\,\mathrm{C/mol}} \ln (1.1 \times 10^{-10}) $$ Rearrange the equation to solve for E°: $$ E^\circ = E + \frac{8.314\,\mathrm{J/mol\cdot K} \times 298.15\,\mathrm{K}}{1 \times 96,485\,\mathrm{C/mol}} \ln (1.1 \times 10^{-10}) $$ E° cannot be determined from the information provided, since we cannot determine the E value from a precipitation reaction. In redox reactions, E can be determined by the balance between reduction potential and oxidation potential, but in precipitation reactions these values are not available.

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Most popular questions from this chapter

Write the equation for the reaction, if any, that occurs when each of the following experiments is performed under standard conditions. (a) Sulfur is added to mercury. (b) Manganese dioxide in acidic solution is added to liquid mercury. (c) Aluminum metal is added to a solution of potassium ions.

For the cell: $$\mathrm{Cr}\left|\mathrm{Cr}^{3+} \| \mathrm{Co}^{2+}\right| \mathrm{Co}$$ \(E^{\circ}\) is \(0.46 \mathrm{~V}\). The same cell was prepared in the laboratory at standard conditions. The voltage obtained was \(0.40 \mathrm{~V}\). A possible explanation for the difference is (a) the surface area of the chromium electrode was smaller than the cobalt electrode. (b) the mass of the chromium electrode was larger than the mass of the cobalt electrode. (c) the concentration of \(\mathrm{Co}\left(\mathrm{NO}_{3}\right)_{2}\) solution used was less than \(1.0 \mathrm{M}\) (d) the concentration of \(\mathrm{Cr}\left(\mathrm{NO}_{3}\right)_{2}\) solution used was less than \(1.0 \mathrm{M}\) (e) the volume of \(\mathrm{Co}\left(\mathrm{NO}_{3}\right)_{2}\) solution used was larger than the volume of \(\mathrm{Cr}\left(\mathrm{NO}_{3}\right)_{2}\) solution used.

Suppose \(E_{\text {red }}^{\circ}\) for \(\mathrm{H}^{+} \longrightarrow \mathrm{H}_{2}\) were taken to be \(0.300 \mathrm{~V}\) instead of \(0.000 \mathrm{~V}\). What would be (a) \(E_{\mathrm{ox}}^{\circ}\) for \(\mathrm{H}_{2} \longrightarrow \mathrm{H}^{+} ?\) (b) \(E_{\text {red }}^{\circ}\) for \(\mathrm{Br}_{2} \longrightarrow \mathrm{Br}^{-}\) ? (c) \(E^{\circ}\) for the cell in \(34(\mathrm{c})\) ? Compare your answer with that obtained in \(34(\mathrm{c})\).

Consider a salt bridge voltaic cell represented by the following reaction $$ \begin{aligned} \mathrm{MnO}_{4}^{-}(a q)+8 \mathrm{H}^{+}(a q)+5 \mathrm{Fe}^{2+}(a q) \longrightarrow & \mathrm{Mn}^{2+}(a q)+5 \mathrm{Fe}^{3+}(a q)+4 \mathrm{H}_{2} \mathrm{O} \end{aligned} $$ (a) What is the direction of the electrons in the external circuit? (b) What electrode can be used at the anode? (c) What is the reaction occurring at the cathode?

A solution containing a metal ion \(\left(\mathrm{M}^{2+}(a q)\right)\) is electrolyzed by a current of 7.8 A. After 15.5 minutes, \(2.39 \mathrm{~g}\) of the metal is plated out. (a) How many coulombs are supplied by the battery? (b) What is the metal? (Assume \(100 \%\) efficiency.)

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