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What reaction will take place at the cathode and the anode when each of the following is electrolyzed? (Assume standard conditions.) a. 1.0 \(M \mathrm{KF}\) solution b. 1.0\(M \mathrm{CuCl}_{2}\) solution c. 1.0 \( M \mathrm{MgI}_{2}\) solution

Short Answer

Expert verified
For the electrolysis of: a. 1.0 M KF solution: Cathode: \(2H_{2}O + 2e^{-} \rightarrow H_{2} (g) + 2OH^{-}\) ; Anode: \(2H_{2}O \rightarrow O_{2} (g) + 4H^{+} + 4e^{-}\) b. 1.0 M CuCl₂ solution: Cathode: \(Cu^{2+} (aq) + 2e^{-} \rightarrow Cu (s)\) ; Anode: \(2Cl^{-} (aq) \rightarrow Cl_{2} (g) + 2e^{-}\) c. 1.0 M MgI₂ solution: Cathode: \(Mg^{2+} (aq) + 2e^{-} \rightarrow Mg (s)\) ; Anode: \(2I^{-} (aq) \rightarrow I_{2} (s) + 2e^{-}\)

Step by step solution

01

Identify the possible reduction and oxidation half-reactions

We first look at the possible reduction half-reaction happening at the cathode: \(F^{-} (aq) + e^{-} \rightarrow F (s)\) The standard reduction potential is -2.87V. This process would require more energy to reduce the F- to F so it is not feasible. Which means that water will get reduced at the cathode to form hydrogen gas and hydroxide ions: \(2H_{2}O + 2e^{-} \rightarrow H_{2} (g) + 2OH^{-}\) Now let's look at the oxidation half-reaction happening at the anode: \(K(s) \rightarrow K^{+} (aq) + e^{-}\) The potential is -2.93V, meaning it is also not feasible. Instead, water oxidation will occur at the anode: \(2H_{2}O \rightarrow O_{2} (g) + 4H^{+} + 4e^{-}\)
02

Write the overall reaction

Combine the two half-reactions at the cathode and the anode: \(2H_{2}O + 2F^{-} (aq) \rightarrow H_{2} (g) + O_{2} (g) + 2OH^{-} (aq) + 2F^{-} (aq)\) b. Electrolysis of 1.0 M CuCl₂ solution
03

Identify the possible reduction and oxidation half-reactions

Possible reduction half-reaction at the cathode: \(Cu^{2+} (aq) + 2e^{-} \rightarrow Cu (s)\) Possible oxidation half-reactions at the anode: \(2Cl^{-} (aq) \rightarrow Cl_{2} (g) + 2e^{-}\)
04

Write the overall reaction

Combine the two half-reactions at the cathode and the anode: \(Cu^{2+} (aq) + 2Cl^{-} (aq) \rightarrow Cu (s) + Cl_{2} (g)\) c. Electrolysis of 1.0 M MgI₂ solution
05

Identify the possible reduction and oxidation half-reactions

Possible reduction half-reaction at the cathode: \(Mg^{2+} (aq) + 2e^{-} \rightarrow Mg (s)\) Possible oxidation half-reactions at the anode: \(2I^{-} (aq) \rightarrow I_{2} (s) + 2e^{-}\)
06

Write the overall reaction

Combine the two half-reactions at the cathode and the anode: \(Mg^{2+} (aq) + 2I^{-} (aq) \rightarrow Mg (s) + I_{2} (s)\)

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Cathode Reaction
In electrolysis, the cathode is the negative electrode where reduction reactions take place. Reducing agents lose electrons here, as opposites attract—positive ions from the solution are drawn to the negatively charged cathode. These ions gain electrons, leading to reduction.

Consider a classic example in electrolysis of a 1.0 M CuCl₂ solution. Here, copper ions, \(Cu^{2+}\), approach the cathode. They gain two electrons each to form solid copper metal:
  • \(Cu^{2+} (aq) + 2e^{-} \rightarrow Cu (s)\)
This process is favorable because the standard reduction potential is positive, making copper deposition efficient.

When dealing with a KF solution, water reduces preferentially over fluoride ions due to a lower potential requirement:
  • \(2H_{2}O + 2e^{-} \rightarrow H_{2} (g) + 2OH^{-}\)
In summary, the cathode hosts reduction reactions, converting ions in solution to their elemental forms or simpler molecules, dependent on electrode potential.
Anode Reaction
The anode in electrolysis is the positive electrode, where oxidation takes place. Here, ions or atoms lose electrons. This loss of electrons results in an oxidation reaction.

In a 1.0 M CuCl₂ solution, chloride ions approach the anode. They lose electrons to form chlorine gas:
  • \(2Cl^{-} (aq) \rightarrow Cl_{2} (g) + 2e^{-}\)
During the electrolysis of 1.0 M MgI₂ solution, iodide ions oxidize upon reaching the anode, resulting in iodine gas formation:
  • \(2I^{-} (aq) \rightarrow I_{2} (s) + 2e^{-}\)
In solutions with water, such as KF, water oxidizes to form oxygen gas:
  • \(2H_{2}O \rightarrow O_{2} (g) + 4H^{+} + 4e^{-}\)
Thus, the anode's oxidation process determines the chemical transformation during electrolysis, relying on potential differences to release electrons.
Redox Reactions
Redox reactions, short for reduction-oxidation reactions, are chemical processes involving the transfer of electrons between two substances. In electrolysis, redox is split into two half-reactions: reduction at the cathode and oxidation at the anode.

These reactions are driven by the application of an external voltage. In the electrolytic cell, this external voltage forces the non-spontaneous reaction of electron flow: from the anode, where oxidation occurs, to the cathode for reduction. Each reaction involves a specific potential that determines the feasibility of the reaction; electrons flow "downhill" energetically speaking.

In electrolysis of a 1.0 M CuCl₂ solution, the anode reaction involves the oxidation of chloride ions, while the cathode sees the reduction of copper ions. These balanced reactions are:
  • Oxidation: \(2Cl^{-} (aq) \rightarrow Cl_{2} (g) + 2e^{-}\)
  • Reduction: \(Cu^{2+} (aq) + 2e^{-} \rightarrow Cu (s)\)
Combining these gives a redox reaction where electrons are transferred from chloride ions to copper ions, leading to elemental chlorine and copper.

Understanding redox reactions helps illuminate the choreography of ions during electrolysis, where electron movement is fundamentally transforming compounds.

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Most popular questions from this chapter

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

An electrochemical cell consists of a standard hydrogen electrode and a copper metal electrode. If the copper electrode is placed in a solution of 0.10\(M \mathrm{NaOH}\) that is saturated with \(\mathrm{Cu}(\mathrm{OH})_{2},\) what is the cell potential at \(25^{\circ} \mathrm{C} ?\left[\text { For } \mathrm{Cu}(\mathrm{OH})_{2}\right.\) \(K_{\mathrm{sp}}=1.6 \times 10^{-19} . ]\)

Sketch the galvanic cells based on the following half- reactions. Show the direction of electron flow, show the direction of ion migration through the salt bridge, and identify the cathode and anode. Give the overall balanced equation, and determine \(\mathscr{E}^{\circ}\) for the galvanic cells. Assume that all concentrations are 1.0 \(M\) and that all partial pressures are 1.0 atm. a. \(\mathrm{H}_{2} \mathrm{O}_{2}+2 \mathrm{H}^{+}+2 \mathrm{e}^{-} \rightarrow 2 \mathrm{H}_{2} \mathrm{O} \quad \mathscr{E}^{\circ}=1.78 \mathrm{V}\) \(\mathrm{O}_{2}+2 \mathrm{H}^{+}+2 \mathrm{e}^{-} \rightarrow \mathrm{H}_{2} \mathrm{O}_{2} \quad \quad \mathscr{E}^{\circ}=0.68 \mathrm{V}\) b. \(\mathrm{Mn}^{2+}+2 \mathrm{e}^{-} \rightarrow \mathrm{Mn} \quad \quad \mathscr{E}^{\circ}=-1.18 \mathrm{V}\) \(\mathrm{Fe}^{3+}+3 \mathrm{e}^{-} \rightarrow \mathrm{Fe} \quad \mathscr{E}^{\circ}=-0.036 \mathrm{V}\)

When magnesium metal is added to a beaker of \(\mathrm{HCl}(\mathrm{aq})\), a gas is produced. Knowing that magnesium is oxidized and that hydrogen is reduced, write the balanced equation for the reaction. How many electrons are transferred in the balanced equation? What quantity of useful work can be obtained when \(\mathrm{Mg}\) is added directly to the beaker of \(\mathrm{HCl}\)? How can you harness this reaction to do useful work?

A chemist wishes to determine the concentration of \(\mathrm{CrO}_{4}^{2-}\) electrochemically. A cell is constructed consisting of a saturated calomel electrode (SCE; see Exercise 111\()\) and a silver wire coated with \(\mathrm{Ag}_{2} \mathrm{CrO}_{4}\) . The \(\mathscr{E}^{\circ}\) value for the following half-reaction is 0.446 \(\mathrm{V}\) relative to the standard hydrogen electrode: $$\mathrm{Ag}_{2} \mathrm{CrO}_{4}+2 \mathrm{e}^{-} \longrightarrow 2 \mathrm{Ag}+\mathrm{CrO}_{4}^{2-}$$ a. Calculate \(\mathscr{E}_{\text { cell } \text { and }} \Delta G\) at \(25^{\circ} \mathrm{C}\) for the cell reaction when \(\left[\mathrm{CrO}_{4}^{2-}\right]=1.00 \mathrm{mol} / \mathrm{L}\) . b. Write the Nernst equation for the cell. Assume that the SCE concentrations are constant. c. If the coated silver wire is placed in a solution (at \(25^{\circ} \mathrm{C} )\) in which \(\left[\mathrm{CrO}_{4}^{2-}\right]=1.00 \times 10^{-5} M,\) what is the expected cell potential? d. The measured cell potential at \(25^{\circ} \mathrm{C}\) is 0.504 \(\mathrm{V}\) when the coated wire is dipped into a solution of unknown \(\left[\mathrm{CrO}_{4}^{2-}\right] .\) What is \(\left[\mathrm{CrO}_{4}^{2-}\right]\) for this solution? e. Using data from this problem and from Table \(18.1,\) calculate the solubility product \(\left(K_{\mathrm{sp}}\right)\) for \(\mathrm{Ag}_{2} \mathrm{CrO}_{4}\).

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