The amount of manganese in steel is determined by changing it to permanganate ion. The steel is first dissolved in nitric acid, producing \(\mathrm{Mn}^{2+}\) ions. These ions are then oxidized to the deeply colored \(\mathrm{MnO}_{4}^{-}\) ions by periodate ion \(\left(\mathrm{IO}_{4}{ }^{-}\right)\) in acid solution. a. Complete and balance an equation describing each of the above reactions. b. Calculate \(\mathscr{E}^{\circ}\) and \(\Delta G^{\circ}\) at \(25^{\circ} \mathrm{C}\) for each reaction.

Short Answer

Expert verified
a. Balanced equations: \( Mn + 2HNO_{3} \rightarrow Mn^{2+} + 2NO_{2} + 2H_{2}O \) \( Mn^{2+} + 2H_{2}IO_{4} + 6H^{+} \rightarrow MnO_{4}^{-} + 2IO_{3}^{-} + 2H_{2}O + 7H^{+} \) b. ℰ⁰ and ΔG⁰: Reaction 1: ℰ⁰: 1.98V ΔG⁰: -383923 J/mol Reaction 2: ℰ⁰: -0.13V ΔG⁰: -62879 J/mol

Step by step solution

01

Balance the dissolution of manganese in steel equation

Here, the steel is first dissolved in nitric acid, producing Mn²⁺ ions. The unbalanced equation can be written as: \( Mn + HNO_{3} \rightarrow Mn^{2+} + NO_{2} + H_{2}O \) To balance the reaction equation, follow the steps mentioned below: - Balance the manganese atoms: The manganese atoms are already balanced. - Balance the hydrogen atoms: There are 4 hydrogen atoms on the left and 2 on the right, so we need to have 2 molecules of water on the right side. - Balance the nitrogen atoms: There are 2 nitrogen atoms on the left, therefore, we need to have 2 molecules of nitric acid on the right side. - Balance the oxygen atoms: There are 6 oxygen atoms on the left and 6 on the right, so they are balanced. The balanced equation is: \( Mn + 2HNO_{3} \rightarrow Mn^{2+} + 2NO_{2} + 2H_{2}O \)
02

Balance the oxidation of Mn²⁺ to MnO₄⁻ by the periodate ion equation

The unbalanced equation can be written as: \( Mn^{2+} + HIO_{4} \rightarrow MnO_{4}^{-} + H^{+} + IO_{3}^{-} \) To balance the reaction equation, the following steps need to be performed: - Balance the manganese atoms: They are already balanced. - Balance the iodine atoms: They are already balanced. - Balance the hydrogen atoms: Place 2 hydrogen atoms on the right side by adding 2 molecules of water and 4 hydrogen atoms on the left by adding 4 protons (H⁺). - Balance the oxygen atoms: Add 2 water molecules on the right side. - Balance the charge: Add 1 extra proton on the right side. The balanced equation is: \( Mn^{2+} + 2H_{2}IO_{4} + 6H^{+} \rightarrow MnO_{4}^{-} + 2IO_{3}^{-} + 2H_{2}O + 7H^{+} \)
03

Calculate ℰ⁰ for each reaction

To calculate the standard potential for each reaction, we can use the standard reduction potentials found in a table. For reaction 1, the half-reactions are: 1. Mn²⁺ +2e⁻ → Mn; ℰ⁰(Mn²⁺/Mn) = -1.18V 2. 2HNO₃ + 2e⁻ → 2NO₂ + 2H₂O; ℰ⁰(NO₂/HNO₃) = 0.8V To find the standard potential of the reaction, ℰ⁰_cell = ℰ⁰(Reduction) - ℰ⁰(Oxidation). \( ℰ_{1}^{\circ}=0.8V-(-1.18)V=1.98V \) For reaction 2, the half-reactions are: 1. Mn²⁺ → MnO₄⁻ + 5e⁻; ℰ⁰(MnO₄⁻/Mn²⁺) = 1.51V 2. HIO₄ + 6e⁻ → 2IO₃⁻ + 2H₂O; ℰ⁰(IO₃⁻/HIO₄) = 1.64V \( ℰ_{2}^{\circ}=1.51V-(1.64)V=-0.13V \)
04

Calculate ΔG⁰ for each reaction

The standard Gibbs free energy change can be calculated using the following formula: ΔG⁰ = -nFℰ⁰ where n is the number of moles of electrons involved in the reaction, F is the Faraday constant (96485 C/mol), and ℰ⁰ is the standard cell potential. For reaction 1 (oxidation), n = 2 mol of electrons. Therefore, \( ΔG_{1}^{\circ}=-2 \times 96485 C/mol \times 1.98V \) \( ΔG_{1}^{\circ}=-383923J/mol \) For reaction 2 (reduction), n = 5 mol of electrons. Therefore, \( ΔG_{2}^{\circ}=-5 \times 96485 C/mol \times (-0.13V) \) \( ΔG_{2}^{\circ}=-62879J/mol \) Final Answers: a. Balanced equations: \( Mn + 2HNO_{3} \rightarrow Mn^{2+} + 2NO_{2} + 2H_{2}O \) \( Mn^{2+} + 2H_{2}IO_{4} + 6H^{+} \rightarrow MnO_{4}^{-} + 2IO_{3}^{-} + 2H_{2}O + 7H^{+} \) b. ℰ⁰ and ΔG⁰: Reaction 1: ℰ⁰: 1.98V ΔG⁰: -383923 J/mol Reaction 2: ℰ⁰: -0.13V ΔG⁰: -62879 J/mol

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Most popular questions from this chapter

The electrolysis of \(\mathrm{BiO}^{+}\) produces pure bismuth. How long would it take to produce \(10.0 \mathrm{~g}\) Bi by the electrolysis of a \(\mathrm{BiO}^{+}\) solution using a current of \(25.0 \mathrm{~A} ?\)

Consider a concentration cell that has both electrodes made of some metal M. Solution A in one compartment of the cell contains \(1.0 M \mathrm{M}^{2+}\). Solution B in the other cell compartment has a volume of \(1.00 \mathrm{~L}\). At the beginning of the experiment \(0.0100\) mole of \(\mathrm{M}\left(\mathrm{NO}_{3}\right)_{2}\) and \(0.0100\) mole of \(\mathrm{Na}_{2} \mathrm{SO}_{4}\) are dissolved in solution \(\mathrm{B}\) (ignore volume changes), where the reaction $$ \mathrm{M}^{2+}(a q)+\mathrm{SO}_{4}{ }^{2-}(a q) \rightleftharpoons \mathrm{MSO}_{4}(s) $$ occurs. For this reaction equilibrium is rapidly established, whereupon the cell potential is found to be \(0.44 \mathrm{~V}\) at \(25^{\circ} \mathrm{C}\). Assume that the process $$ \mathrm{M}^{2+}+2 \mathrm{e}^{-} \longrightarrow \mathrm{M} $$ has a standard reduction potential of \(-0.31 \mathrm{~V}\) and that no other redox process occurs in the cell. Calculate the value of \(K_{\text {sp }}\) for \(\operatorname{MSO}_{4}(s)\) at \(25^{\circ} \mathrm{C}\).

Which of the following statements concerning corrosion is(are) true? For the false statements, correct them. a. Corrosion is an example of an electrolytic process. b. Corrosion of steel involves the reduction of iron coupled with the oxidation of oxygen. c. Steel rusts more easily in the dry (arid) Southwest states than in the humid Midwest states. d. Salting roads in the winter has the added benefit of hindering the corrosion of steel. e. The key to cathodic protection is to connect via a wire a metal more easily oxidized than iron to the steel surface to be protected.

The overall reaction in the lead storage battery is \(\mathrm{Pb}(s)+\mathrm{PbO}_{2}(s)+2 \mathrm{H}^{+}(a q)+2 \mathrm{HSO}_{4}^{-}(a q) \longrightarrow\) \(2 \mathrm{PbSO}_{4}(s)+2 \mathrm{H}_{2} \mathrm{O}(l)\) a. For the cell reaction \(\Delta H^{\circ}=-315.9 \mathrm{~kJ}\) and \(\Delta S^{\circ}=\) \(263.5 \mathrm{~J} / \mathrm{K}\). Calculate \(\mathscr{E}^{\circ}\) at \(-20 .{ }^{\circ} \mathrm{C}\). Assume \(\Delta H^{\circ}\) and \(\Delta S^{\circ}\) do not depend on temperature. b. Calculate \(\mathscr{E}\) at \(-20 .{ }^{\circ} \mathrm{C}\) when \(\left[\mathrm{HSO}_{4}{ }^{-}\right]=\left[\mathrm{H}^{+}\right]=4.5 M\). c. Consider your answer to Exercise 71 . Why does it seem that batteries fail more often on cold days than on warm days?

Is the following statement true or false? Concentration cells work because standard reduction potentials are dependent on concentration. Explain.

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