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Explain why E^(@) for Mn^(3+)// Mn^(@+) couple is more positive than that for Fe^(3+) //Fe^(2+)( At. Nos. Mn= 25, Fe= 26) ? Or Why is +2 oxidation state of manganese quite stablewhile the same is not true for iron ? [Mn= 25 , Fe = 26]

Answer»

Solution :`._(25)Mn^(2+) = [Ar] 3D^(5), . _(25) Mn^(3+) =[Ar] 3d^(4), ._(26) Fe^(2+) = [ Ar] 3d^(6) , . _(26) Fe^(3+)= [ Ar] 3d^(5)`
Thus, `Mn^(2+)` has more stable configurationthan `Mn^(3+)` while `Fe^(3+)`has more stable then `Fe^92+)`. Consequently, large third ionisation enthalpy is REQUIRED to change `Mn^(2+)` to `Mn^(3+)`. As `E^(@)` is the sum of enthalpy of atomisation, IONIZATION enthalpy and hydration enthalpy, THEREFORE, `E^(@)` for `Mn^(3+)//Mn^(2+)` couple is more positive than `Fe^(3+) //Fe^(2+)` .
Note `,` The large positive `E^(@)` for `Mn^(3+)//Mn^(2+)` means that `Mn^(3+)` can be easily reduced to `Mn^(2+)` , i.e. `Mn^(3+)` is less stable . `E^(@)` value for `Fe^(3+) //Fe^2+)` is positive but SMALL, i.e., `Fe^(3+)` can also be reducedto `Fe^(2+)` but less easily. Thus,`Fe^(3+)` is more stable than `Mn^(3+)` . It also explains why `+3` state of Mn is of little importance.


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