Chapter 18: Problem 31
Consider the electrolysis of a molten salt of some metal. What information must you know to calculate the mass of metal plated out in the electrolytic cell?
Chapter 18: Problem 31
Consider the electrolysis of a molten salt of some metal. What information must you know to calculate the mass of metal plated out in the electrolytic cell?
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Get started for freeThe black silver sulfide discoloration of silverware can be removed by heating the silver article in a sodium carbonate solution in an aluminum pan. The reaction is $$3 \mathrm{Ag}_{2} \mathrm{S}(s)+2 \mathrm{Al}(s) \rightleftharpoons 6 \mathrm{Ag}(s)+3 \mathrm{S}^{2-}(a q)+2 \mathrm{Al}^{3+}(a q)$$ a. Using data in Appendix \(4,\) calculate \(\Delta G^{\circ}, K,\) and \(\mathscr{E}^{\circ}\) for the above reaction at $25^{\circ} \mathrm{C} .\left[\text { For } \mathrm{Al}^{3+}(a q), \Delta G_{\mathrm{f}}^{\circ}=-480 . \mathrm{kJ} / \mathrm{mol.}\right]$ b. Calculate the value of the standard reduction potential for the following half-reaction: $$2 \mathrm{e}^{-}+\mathrm{Ag}_{2} \mathrm{S}(s) \longrightarrow 2 \mathrm{Ag}(s)+\mathrm{S}^{2-}(a q)$$
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.
Three electrochemical cells were connected in series so that the same quantity of electrical current passes through all three cells. In the first cell, 1.15 g chromium metal was deposited from a chromium (III) nitrate solution. In the second cell, 3.15 \(\mathrm{g}\) osmium was deposited from a solution made of \(\mathrm{Os}^{n+}\) and nitrate ions. What is the name of the salt? In the third cell, the electrical charge passed through a solution containing \(\mathrm{X}^{2+}\) ions caused deposition of 2.11 \(\mathrm{g}\) metallic \(\mathrm{X}\) . What is the electron configuration of \(\mathrm{X} ?\)
In the electrolysis of an aqueous solution of $\mathrm{Na}_{2} \mathrm{SO}_{4},$ what reactions occur at the anode and the cathode (assuming standard conditions)? $$\begin{array}{ll} {\text{}} & \quad{ \mathscr{E}^{\circ} } \\ \hline {\mathrm{S}_{2} \mathrm{O}_{8}^{2-}+2 \mathrm{e}^{-} \longrightarrow 2 \mathrm{SO}_{4}^{2-}} & {2.01 \mathrm{V}} \\ {\mathrm{O}_{2}+4 \mathrm{H}^{+}+4 \mathrm{e}^{-} \longrightarrow 2 \mathrm{H}_{2} \mathrm{O}} & {1.23 \mathrm{V}} \\ {2 \mathrm{H}_{2} \mathrm{O}+2 \mathrm{e}^{-} \longrightarrow \mathrm{H}_{2}+2 \mathrm{OH}^{-}} & {-0.83 \mathrm{V}} \\\ {\mathrm{Na}^{+}+\mathrm{e}^{-} \longrightarrow \mathrm{Na}} & {-2.71 \mathrm{V}}\end{array}$$
A galvanic cell is based on the following half-reactions: $$\mathrm{Cu}^{2+}(a q)+2 \mathrm{e}^{-} \longrightarrow \mathrm{Cu}(s) \quad \mathscr{E}^{\circ}=0.34 \mathrm{V}$$ $$\mathrm{V}^{2+}(a q)+2 \mathrm{e}^{-} \longrightarrow \mathrm{V}(s) \quad \mathscr{E}^{\circ}=-1.20 \mathrm{V}$$ In this cell, the copper compartment contains a copper electrode and \(\left[\mathrm{Cu}^{2+}\right]=1.00 M,\) and the vanadium compartment contains a vanadium electrode and \(\mathrm{V}^{2+}\) at an unknown concentration. The compartment containing the vanadium \((1.00 \mathrm{L}\) of solution) was titrated with 0.0800\(M \mathrm{H}_{2} \mathrm{EDTA}^{2-}\) , resulting in the reaction $$\mathrm{H}_{2} \mathrm{EDTA}^{2-}(a q)+\mathrm{V}^{2+}(a q) \rightleftharpoons \mathrm{VEDTA}^{2-}(a q)+2 \mathrm{H}^{+}(a q)$$ $$\quad\quad\quad\quad\quad\quad\quad\quad\quad\quad\quad\quad\quad\quad\quad\quad\quad\quad\quad\quad\quad\quad K=?$$ The potential of the cell was monitored to determine the stoichiometric point for the process, which occurred at a volume of 500.0 $\mathrm{mL} \mathrm{H}_{2} \mathrm{EDTA}^{2-}$ solution added. At the stoichiometric point, \(\mathscr{E}_{\text {cell}}\) was observed to be 1.98 \(\mathrm{V}\) . The solution was buffered at a pH of 10.00 . a. Calculate\(\mathscr{E}_{\text {cell}}\) before the titration was carried out. b. Calculate the value of the equilibrium constant, \(K\), for the titration reaction. c. Calculate \(\mathscr{E}_{\text {cell}}\) at the halfway point in the titration.
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