→ One of the notable features of a transition element is the great variety of oxidation states it may show in its compounds.
| Sc | Ti | V | Cr | Mn | Fe | Co | Ni | Cu | Zn |
| | +2 | +2 | +2 | +2 | +2 | +2 | +2 | +1 | +2 |
| +3 | +3 | +3 | +3 | +3 | +3 | +3 | +3 | +2 | |
| | +4 | +4 | +4 | +4 | +4 | +4 | +4 | | |
| | | +5 | +5 | +5 | | | | | |
| | | | +6 | +6 | +6 | | | | |
| | | | | +7 | | | | | |
Oxidation States of the first row Transition Metals
(the most common ones are in bold types)
→ The elements which give the greatest number of oxidation states occur in or near the middle of the series. Manganese, for example, exhibits all the oxidation states from +2 to +7.
→ In the starting of series, very less number of d-electrons are available for chemical bonding. Hence, less number of oxidation states are shown by elements present at the starting of series.
e.g.: Sc
+3, Ti
+2, Ti
+3, Ti
+4 → At the end of the series there are too many d-electrons and d-orbitals are completely occupied. Hence, these elements show very less number of oxidation states.
→ Down the group the stability of elements in higher oxidation states increases because removal of electrons from d-orbitals become easy.
→ For example, in group 6, Mo(VI) and W(VI) are found to be more stable than Cr(VI). Thus, Cr(VI) in the form of dichromate in acidic medium is a strong oxidising agent, whereas MoO
3 and WO
3 are not.
→ Low oxidation states are found when a complex compound has ligands capable of π-acceptor character in addition to the o-bonding. For example, in Ni(CO)
4 and Fe(CO)
5, the oxidation state of nickel and iron is zero.