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NCERT Exemplar · Q16

Q.KMnO4KMnO_4 acts as an oxidising agent in alkaline medium. When alkaline KMnO4KMnO_4 is treated with KI, iodide ion is oxidised to ____________.

(i) I2I_2
(ii) IO−IO^-
(iii) IO3−IO_3^-
(iv) IO4−IO_4^-
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In alkaline medium, KMnO4KMnO_4 is reduced to MnO2MnO_2 (or MnO42−MnO_4^{2-}) and oxidises IX−\ce{I-} all the way to iodate (IO3−IO_3^-), not just iodine. The correct option is (iii).

The key to this question lies in understanding how the oxidising power of KMnO4KMnO_4 changes with pH. In acidic medium, MnO4−MnO_4^- is reduced to MnX2+\ce{Mn^{2+}} (a 5-electron change) and is a very strong oxidant — it can oxidise IX−\ce{I-} to I2I_2 easily. But in alkaline medium, the reduction product is different, and so is the extent of oxidation it can achieve.

When the medium is alkaline, MnO4−MnO_4^- typically reduces to MnO2MnO_2 (manganese dioxide, oxidation state +4) or, in strongly alkaline conditions, to manganate ion MnO42−MnO_4^{2-} (oxidation state +6). The number of electrons gained per MnO4−MnO_4^- is smaller (3 electrons for MnO2MnO_2, 1 electron for MnO42−MnO_4^{2-}), so the oxidising power per mole is less intense. However, the reaction is still vigorous enough to push iodide beyond elemental iodine.

Iodide ion IX−\ce{I-} (oxidation state -1) can be oxidised stepwise: first to I2I_2 (0), then to hypoiodite IO−IO^- (+1), then to iodite IO2−IO_2^- (+3), then to iodate IO3−IO_3^- (+5), and finally to periodate IO4−IO_4^- (+7). In alkaline medium, KMnO4KMnO_4 is strong enough to take it to the +5 state — iodate — but not to periodate (which requires even stronger oxidants or specific conditions like hot alkaline KMnO4KMnO_4 with a catalyst).

Let’s walk through the actual reaction.

  1. Identify the half-reactions. In alkaline medium, the reduction half-reaction for permanganate is:

MnO4−+2H2O+3e−→MnO2+4OH−MnO_4^- + 2H_2O + 3e^- \rightarrow MnO_2 + 4OH^-

(This is the most common version; in very concentrated alkali, MnO42−MnO_4^{2-} forms instead, but the principle is the same.)

  1. Oxidation half-reaction for iodide. Iodide is oxidised to iodate:

I−+6OH−→IO3−+3H2O+6e−I^- + 6OH^- \rightarrow IO_3^- + 3H_2O + 6e^-

  1. Balance the electrons. The reduction consumes 3 electrons per MnO4−MnO_4^-, the oxidation produces 6 electrons per I−I^-. To balance, we need 2 MnO4−MnO_4^- for every 1 I−I^-:

2MnO4−+4H2O+6e−→2MnO2+8OH−2MnO_4^- + 4H_2O + 6e^- \rightarrow 2MnO_2 + 8OH^-

I−+6OH−→IO3−+3H2O+6e−I^- + 6OH^- \rightarrow IO_3^- + 3H_2O + 6e^-

  1. Add the two half-reactions. Cancel water and hydroxide where possible: …

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