Electrochemistry: Question 9

Syllabus 24.2

Multiple choice A2 1 mark

The table below gives the standard electrode potentials of four metal/metal-ion half-cells:

Half-equation EE^{\ominus} / V
Mg2+(aq)+2eMg(s)\text{Mg}^{2+}(aq) + 2e^- \rightleftharpoons \text{Mg}(s) 2.37-2.37
Zn2+(aq)+2eZn(s)\text{Zn}^{2+}(aq) + 2e^- \rightleftharpoons \text{Zn}(s) 0.76-0.76
Fe2+(aq)+2eFe(s)\text{Fe}^{2+}(aq) + 2e^- \rightleftharpoons \text{Fe}(s) 0.44-0.44
Cu2+(aq)+2eCu(s)\text{Cu}^{2+}(aq) + 2e^- \rightleftharpoons \text{Cu}(s) +0.34+0.34

Based only on these standard electrode potentials, which of the following reactions is feasible under standard conditions?

Choose an answer to check it, then compare with the worked solution below.

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Worked solution

Step 1: Set up the rule for feasibility

For a reaction written as (metal X is oxidised) + (metal ion Y\textsuperscript{n+} is reduced) \rightarrow (metal X ion) + (metal Y), the metal ion couple that is reduced is the cathode and the metal couple that is oxidised is the anode:

Ecell=E(cathode, species reduced)E(anode, species oxidised)E_{cell}^{\ominus} = E^{\ominus}(\text{cathode, species reduced}) - E^{\ominus}(\text{anode, species oxidised})

The reaction is feasible under standard conditions only if Ecell>0E_{cell}^{\ominus} > 0.

Step 2: Test each option

A: Cu(s)+Fe2+(aq)Cu2+(aq)+Fe(s)\text{Cu}(s) + \text{Fe}^{2+}(aq) \rightarrow \text{Cu}^{2+}(aq) + \text{Fe}(s). Here Fe2+\text{Fe}^{2+} is reduced (cathode, 0.44 V-0.44\ \text{V}) and Cu\text{Cu} is oxidised (anode, +0.34 V+0.34\ \text{V}): Ecell=(0.44)(+0.34)=0.78 V(not feasible)E_{cell}^{\ominus} = (-0.44) - (+0.34) = -0.78\ \text{V} \quad (\text{not feasible})

B: Fe(s)+Mg2+(aq)Fe2+(aq)+Mg(s)\text{Fe}(s) + \text{Mg}^{2+}(aq) \rightarrow \text{Fe}^{2+}(aq) + \text{Mg}(s). Here Mg2+\text{Mg}^{2+} is reduced (cathode, 2.37 V-2.37\ \text{V}) and Fe\text{Fe} is oxidised (anode, 0.44 V-0.44\ \text{V}): Ecell=(2.37)(0.44)=1.93 V(not feasible)E_{cell}^{\ominus} = (-2.37) - (-0.44) = -1.93\ \text{V} \quad (\text{not feasible})

C: Zn(s)+Fe2+(aq)Zn2+(aq)+Fe(s)\text{Zn}(s) + \text{Fe}^{2+}(aq) \rightarrow \text{Zn}^{2+}(aq) + \text{Fe}(s). Here Fe2+\text{Fe}^{2+} is reduced (cathode, 0.44 V-0.44\ \text{V}) and Zn\text{Zn} is oxidised (anode, 0.76 V-0.76\ \text{V}): Ecell=(0.44)(0.76)=+0.32 V(feasible, Ecell>0)E_{cell}^{\ominus} = (-0.44) - (-0.76) = +0.32\ \text{V} \quad (\text{feasible, } E_{cell}^{\ominus} > 0)

D: Cu(s)+Zn2+(aq)Cu2+(aq)+Zn(s)\text{Cu}(s) + \text{Zn}^{2+}(aq) \rightarrow \text{Cu}^{2+}(aq) + \text{Zn}(s). Here Zn2+\text{Zn}^{2+} is reduced (cathode, 0.76 V-0.76\ \text{V}) and Cu\text{Cu} is oxidised (anode, +0.34 V+0.34\ \text{V}): Ecell=(0.76)(+0.34)=1.10 V(not feasible)E_{cell}^{\ominus} = (-0.76) - (+0.34) = -1.10\ \text{V} \quad (\text{not feasible})

Step 3: Interpret the result

Only reaction C gives a positive EcellE_{cell}^{\ominus}. This matches the electrochemical series: zinc lies below iron in the table (more negative EE^{\ominus}), meaning zinc is a stronger reducing agent than iron and readily loses electrons to Fe2+(aq)\text{Fe}^{2+}(aq), displacing iron from solution. In every other option, the metal being oxidised is actually the weaker reducing agent of the pair (i.e. it lies above, or has a more positive EE^{\ominus} than, the ion it is supposedly reducing), so those reactions run in the thermodynamically unfavourable direction.

Final answer

  • The only feasible reaction under standard conditions is Zn(s)+Fe2+(aq)Zn2+(aq)+Fe(s)\text{Zn}(s) + \text{Fe}^{2+}(aq) \rightarrow \text{Zn}^{2+}(aq) + \text{Fe}(s), with Ecell=+0.32 VE_{cell}^{\ominus} = +0.32\ \text{V}, option C.