A green solution of potassium manganate, K2MnO4, is made acidic. Which manganese-containing products are formed?
Answer & explanation
Correct answer: option 4
The correct answer is Option (4) → \( \ce{MnO4^-} \) and \( \ce{MnO2} \)
Manganese(VI) in the manganate ion is unstable in acid solution. It undergoes disproportionation: part of it is oxidised to a higher state and part is reduced to a lower state.
Manganate, MnO42−: Mn is +6.
Permanganate, MnO4−: Mn is +7 (oxidised, one electron lost per Mn).
Manganese dioxide, MnO2: Mn is +4 (reduced, two electrons gained per Mn).
Electrons balance when two Mn are oxidised for every one reduced, so 3 manganate ions give 2 permanganate ions and 1 MnO2.
\( \displaystyle \ce{3MnO4^2- + 4H+ -> 2MnO4^- + MnO2 + 2H2O} \)
This step is used in the preparation of potassium permanganate from the dark green K2MnO4.
Why the other options are incorrect
Option (1) \( \ce{MnO4^-} \) and \( \ce{Mn^2+} \) — Incorrect. Mn2+ is formed when acidified permanganate oxidises a reducing agent such as Fe2+ or I−. In acid, manganate gives MnO2 (Mn +4) as its lower product.
Option (2) \( \ce{MnO4^-} \) only — Incorrect.
If every Mn went from +6 to +7, the electrons would have to be taken by an oxidising agent.
Permanganate alone is obtained when manganate is oxidised, as in the commercial electrolytic oxidation; simple acidification gives a lower product as well.
Option (3) \( \ce{MnO2} \) and \( \ce{Mn^2+} \) — Incorrect. Both have oxidation states below +6. Manganese would then only be reduced, with nothing oxidised, which is not possible without a reducing agent.
NCERT (2026-27 edition):
Example 4.9 – “When a particular oxidation state becomes less stable relative to other oxidation states, one lower, one higher, it is said to undergo disproportionation. For example, manganese (VI) becomes unstable relative to manganese(VII) and manganese (IV) in acidic solution.
3MnVIO42– + 4 H+ → 2 MnVIIO4– + MnIVO2 + 2H2O”
4.4.1 Oxides and Oxoanions of Metals – “Potassium permanganate is prepared by fusion of MnO2 with an alkali metal hydroxide and an oxidising agent like KNO3. This produces the dark green K2MnO4 which disproportionates in a neutral or acidic solution to give permanganate.”