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Asked by Venkat Last Modified
These are interesting observations that can be explained by considering the electronic configurations and trends in oxidation states across transition metals.
(i) Cr2+ is reducing in nature while Mn3+ is an oxidizing agent: This can be explained by looking at the electronic configurations of Cr2+ and Mn3+.
Cr2+ has an electronic configuration of [Ar] 3d4, where it has a half-filled d orbital. Half-filled orbitals have lower energy due to greater exchange energy, making it energetically favorable for Cr2+ to lose electrons and become Cr3+ in order to achieve a stable half-filled d orbital, thus acting as a reducing agent.
On the other hand, Mn3+ has an electronic configuration of [Ar] 3d4, which is one electron short of achieving a stable half-filled d orbital. So, Mn3+ tends to gain an electron to achieve a stable half-filled d orbital, making it an oxidizing agent as it oxidizes other species by accepting electrons.
(ii) In a transition series of metals, the metal which exhibits the greatest number of oxidation states occurs in the middle of the series: This observation can be explained by considering the trends in the filling of d orbitals across the transition series.
At the beginning of the transition series, elements have fewer d electrons available for oxidation, limiting the number of oxidation states they can exhibit.
Toward the middle of the series, there's a peak in the number of oxidation states exhibited. This is because these elements have a balance between gaining and losing electrons, allowing them to exhibit a wider range of oxidation states.
Towards the end of the series, the number of oxidation states generally decreases as elements have a higher tendency to gain electrons rather than lose them, leading to fewer oxidation states.
So, the middle of the transition series tends to have elements that can exhibit the greatest number of oxidation states due to the balance between gaining and losing electrons facilitated by their electronic configurations.
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