Metallic gold is collected from below the anode when a mixture of copper and gold metals is refined by electrolysis. Explain this behavior.

Short Answer

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In the electrolysis of a copper-gold mixture, metallic gold is collected below the anode due to the differences in redox potentials between the two metals. Copper has a lower redox potential and is more prone to oxidation at the anode and reduction at the cathode. Gold, with a higher redox potential, remains in the electrolyte solution and settles down below the anode due to its higher density.

Step by step solution

01

Understanding electrolysis

Electrolysis is a process that uses an electric current to drive a non-spontaneous chemical reaction. In the case of refining metals, this will involve the dissolution of the metal at the anode (positive electrode) and its deposition at the cathode (negative electrode). This is done in an electrolyte solution which facilitates the flow of ions between the electrodes.
02

Understanding the behavior of copper and gold in electrolysis

Both copper and gold are metals that have positive redox potentials, which means they are generally more resistant to oxidation (loss of electrons) and more likely to undergo reduction (gain of electrons). In an electrolytic cell, the metal that has the highest redox potential will have the greatest tendency to be reduced at the cathode, while the metal with the lower redox potential will oxidize more readily at the anode.
03

Comparing redox potentials of copper and gold

Although both copper and gold have positive redox potentials, gold has a higher redox potential than copper. Gold has a reduction potential of +1.50 V while copper has a reduction potential of +0.337 V. This means gold is less prone to oxidation and more prone to reduction than copper.
04

Explaining the behavior of gold in the electrolysis of copper and gold

Based on the redox potentials, when a mixture of copper and gold is subjected to electrolysis, copper is more likely to be oxidized at the anode compared to gold. This is because copper has a lower redox potential, therefore it will readily lose electrons to form Cu(2+) ions in the electrolyte. At the cathode, gold ions will be more likely to undergo reduction due to their higher redox potential. However, when copper ions are present in the solution, they will preferentially reduce at the cathode, forming copper metal. As a result, gold ions will not efficiently deposit onto the cathode and will instead remain in the electrolyte solution. Since gold has a higher density than the electrolyte solution, the gold ions in the solution will gradually settle down due to gravity, forming a layer of metallic gold below the anode. So in conclusion, metallic gold is collected from below the anode during the electrolysis of a mixture of copper and gold because of the differences in the redox potentials between the two metals. Copper is more likely to be oxidized at the anode and reduced at the cathode, while gold remains in the electrolyte solution and eventually settles down due to its higher density.

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Most popular questions from this chapter

Copper corrodes to cuprous oxide, \(\mathrm{Cu}_{2} \mathrm{O},\) or cupric oxide, \(\mathrm{CuO},\) depending on environmental conditions. (a) What is the oxidation state of copper in cuprous oxide? (b) What is the oxidation state of copper in cupric oxide? (c) Copper peroxide is another oxidation product of elemental copper. Suggest a formula for copper peroxide based on its name. (d) Copper(III) oxide is another unusual oxidation product of elemental copper. Suggest a chemical formula for copper(III) oxide.

Indicate whether each of the following statements is true or false: (a) If something is oxidized, it is formally losing electrons. (b) For the reaction $\mathrm{Fe}^{3+}(a q)+\mathrm{Co}^{2+}(a q) \longrightarrow \mathrm{Fe}^{2+}(a q)+\( \)\mathrm{Co}^{3+}(a q), \mathrm{Fe}^{3+}(a q)\( is the reducing agent and \)\mathrm{Co}^{2+}(a q)$ is the oxidizing agent. (c) If there are no changes in the oxidation state of the reactants or products of a particular reaction, that reaction is not a redox reaction.

A voltaic cell is constructed with two \(\mathrm{Cu}^{2+}-\mathrm{Cu}\) electrodes. The two half-cells have $\left[\mathrm{Cu}^{2+}\right]=0.100 \mathrm{M}\( and \)\left[\mathrm{Cu}^{2+}\right]=1.00 \times 10^{-4} \mathrm{M}$, respectively. (a) Which electrode is the cathode of the cell? (b) What is the standard emf of the cell? (c) What is the cell emf for the concentrations given? (d) For each electrode, predict whether \(\left[\mathrm{Cu}^{2+}\right]\) will increase, decrease, or stay the same as the cell operates.

A student designs an ammeter (device that measures electrical current) that is based on the electrolysis of water into hydrogen and oxygen gases. When electrical current of unknown magnitude is run through the device for 90 min, \(32.5 \mathrm{~mL}\) of water-saturated \(\mathrm{H}_{2}(g)\) is collected. The temperature of the system is \(20^{\circ} \mathrm{C},\) and the atmospheric pressure is \(101.3 \mathrm{kPa}\). What is the magnitude of the average current in amperes?

Cytochrome, a complicated molecule that we will represent as \(\mathrm{CyFe}^{2+}\), reacts with the air we breathe to supply energy required to synthesize adenosine triphosphate (ATP). The body uses ATP as an energy source to drive other reactions (Section 19.7). At \(\mathrm{pH} 7.0\) the following reduction potentials pertain to this oxidation of \(\mathrm{CyFe}^{2+}\) $$ \begin{aligned} \mathrm{O}_{2}(g)+4 \mathrm{H}^{+}(a q)+4 \mathrm{e}^{-} & \longrightarrow 2 \mathrm{H}_{2} \mathrm{O}(l) & & E_{\mathrm{red}}^{\circ}=+0.82 \mathrm{~V} \\\ \mathrm{CyFe}^{3+}(a q)+\mathrm{e}^{-} & \longrightarrow \mathrm{CyFe}^{2+}(a q) & E_{\mathrm{red}}^{\circ} &=+0.22 \mathrm{~V} \end{aligned} $$ (a) What is \(\Delta G\) for the oxidation of \(\mathrm{CyFe}^{2+}\) by air? \((\mathbf{b})\) If the synthesis of \(1.00 \mathrm{~mol}\) of ATP from adenosine diphosphate (ADP) requires a \(\Delta G\) of \(37.7 \mathrm{~kJ},\) how many moles of ATP are synthesized per mole of \(\mathrm{O}_{2} ?\)

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