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Intext Questions · 2.3

Q.Consult the table of standard electrode potentials and suggest three substances that can oxidise ferrous ions under suitable conditions.

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The key idea is that a substance can oxidise FeX2+\ce{Fe^{2+}} to FeX3+\ce{Fe^{3+}} if its standard reduction potential is greater than +0.77 V+0.77\ \text{V} (the E∘E^\circ for FeX3+/FeX2+\ce{Fe^{3+}/Fe^{2+}}). Three such oxidising agents are FX2\ce{F2}, ClX2\ce{Cl2}, and OX3\ce{O3}.

Why Standard Electrode Potentials Decide the Reaction

Oxidation is the loss of electrons. For FeX2+\ce{Fe^{2+}} to be oxidised to FeX3+\ce{Fe^{3+}}, it must give away an electron. That electron must be accepted by some other species — the oxidising agent. The tendency of a species to accept electrons is measured by its standard reduction potential (E∘E^\circ). The more positive the E∘E^\circ, the stronger the oxidising agent.

The half-reaction for ferrous oxidation is:

FeX3++eX−→FeX2+E∘=+0.77 V\ce{Fe^{3+} + e- -> Fe^{2+}} \quad E^\circ = +0.77\ \text{V}

This value tells us that FeX3+\ce{Fe^{3+}} has a moderate tendency to get reduced back to FeX2+\ce{Fe^{2+}}. To push the reaction in the opposite direction — to force FeX2+\ce{Fe^{2+}} to lose an electron — we need an oxidising agent that is even more eager to gain electrons. In other words, the oxidising agent's reduction potential must be greater than +0.77 V+0.77\ \text{V}.

A species X can oxidise FeX2+\ce{Fe^{2+}} to FeX3+\ce{Fe^{3+}} if:

E∘(X/X−)>+0.77 VE^\circ(\text{X}/\text{X}^-) > +0.77\ \text{V}

Step-by-step selection

  1. Recall the standard reduction potentials of common oxidising agents. From the standard table (at 25∘C25^\circ\text{C}, 1 atm1\ \text{atm}, 1 M1\ \text{M}), we have:

    • FX2+2 eX−→2 FX−\ce{F2 + 2e- -> 2F-}: E∘=+2.87 VE^\circ = +2.87\ \text{V}
    • OX3+2 HX++2 eX−→OX2+HX2O\ce{O3 + 2H+ + 2e- -> O2 + H2O}: E∘=+2.07 VE^\circ = +2.07\ \text{V}
    • ClX2+2 eX−→2 ClX−\ce{Cl2 + 2e- -> 2Cl-}: E∘=+1.36 VE^\circ = +1.36\ \text{V}
    • MnOX4X−+8 HX++5 eX−→MnX2++4 HX2O\ce{MnO4- + 8H+ + 5e- -> Mn^{2+} + 4H2O}: E∘=+1.51 VE^\circ = +1.51\ \text{V}
    • CrX2OX7X2−+14 HX++6 eX−→2 CrX3++7 HX2O\ce{Cr2O7^{2-} + 14H+ + 6e- -> 2Cr^{3+} + 7H2O}: E∘=+1.33 VE^\circ = +1.33\ \text{V}
    • BrX2+2 eX−→2 BrX−\ce{Br2 + 2e- -> 2Br-}: E∘=+1.09 VE^\circ = +1.09\ \text{V}
    • IX2+2 eX−→2 IX−\ce{I2 + 2e- -> 2I-}: E∘=+0.54 VE^\circ = +0.54\ \text{V}
  2. Compare each with +0.77 V+0.77\ \text{V}. Any species with E∘>0.77 VE^\circ > 0.77\ \text{V} can, in principle, oxidise FeX2+\ce{Fe^{2+}}. Those with E∘<0.77 VE^\circ < 0.77\ \text{V} (like IX2\ce{I2}) cannot.

  3. Select three distinct substances that are commonly available and clearly satisfy the condition. Good choices are:

    • Fluorine gas (FX2\ce{F2}): E∘=+2.87 VE^\circ = +2.87\ \text{V} — the strongest oxidising agent known.
    • Chlorine gas (ClX2\ce{Cl2}): E∘=+1.36 VE^\circ = +1.36\ \text{V} — a classic laboratory oxidiser.
    • Ozone (OX3\ce{O3}): E∘=+2.07 VE^\circ = +2.07\ \text{V} — a powerful oxidant used in water treatment.

    Other valid options include KMnOX4\ce{KMnO4} (acidified), KX2CrX2OX7\ce{K2Cr2O7} (acidified), or BrX2\ce{Br2}, but the question asks for three substances, and the above are unambiguous. …

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