For M2+/M and M3+/M2+ systems the E° values for some metals are as follows:
Cr2+/Cr – 0.9 V Cr3+/Cr2+ – 0.4 V
Mn2+/Mn – 1.2 V Mn3+/Mn2+ + 1.5 V
Fe2+/Fe – 0.4 V Fe3+/Fe2+ + 0.8 V
Use this data to comment upon
(a) The stability of Fe3+ in acid solution as compared to that of Cr3+ or Mn3+ and
(b) In case with which iron can be oxidised as compared to the similar process for either chromium or manganese metal
Predict which of the following will be coloured in aqueous solution? Ti3+, V3+, Cu+, Sc3+, Mn2+, Fe3+ and Co2+. Give reason for each.
Compare the chemistry of actinides with that of the lanthanoids with special reference to:
(i) electronic configuration, (ii) atomic and ionic sizes, (iii) oxidation state (iv) chemical reactivity.
How would you account for the following:
(a) Of the d4 species, Cr2+ is strongly reducing while manganese(III) is strongly oxidising.
(b) Cobalt(II) is stable in aqueous solution but in the presence of complexing reagents it is easily oxidized.
(c) The d1 configuration is very unstable in ions.
(a) Of d4 species, Cr2+ has 3d4 configuration and tends to loose one electron to acquire d3 configuration as it is highly stable and best metallic specie available for complex formation. Cr3+can accommodate six lone pair of electrons from ligands due to sp3d2 hybridisation e.g. [Cr(NH3)6]3+ Mn3+ although have d4 configuration but tends to become Mn2+ stable specie by acquiring one electron to attain d5 configuration. It becomes exactly half filled on one hand and more energy is released in gain of electron due to higher nuclear charge.
(b) Co2+ is stable in aqueous solution because it get surrounded and weakly bonded to water molecules. In presence of strong ligands and air it gets oxidised to Co(III) as strong ligands get coordinated more strongly with Co(III). The electronic configuration of Co(II) and Co(III) are:
Co(II) = [Ar]18 4s03d7 and
Co(III) = [Ar]184s03d6
In Co(III) specie, 6 lone pairs of electrons from ligands are accommodated by sp3d2hybridisation which is not possible in Co(II).
(c) Some species with d1 configuration are reducing and tends to loose one electron to acquire d4 stable configuration. Some other species with d1 configuration like Cr(V) and Mn(VI) undergo disproportionation.