Q.Compare the chemistry of the actinoids with that of lanthanoids with reference to:
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Start your 14-day free trial to unlock the full solution →Actinoids show greater variability in electronic configuration, a wider range of oxidation states, and higher chemical reactivity than lanthanoids, primarily due to the weaker shielding and smaller energy gap between the 5f, 6d, and 7s orbitals.
Why the Actinoids Are More "Restless" Than the Lanthanoids
The lanthanoids and actinoids are both inner transition series, filling the 4f and 5f orbitals respectively. But the chemistry of the actinoids is far richer and more complex. The root cause is a single quantum mechanical fact: the 5f orbitals are less effectively shielded from the nucleus than the 4f orbitals. This means 5f electrons are held less tightly, have higher energy, and are more available for bonding and oxidation. The 4f orbitals, by contrast, are buried deep inside the atom and are notoriously "chemically inert."
Let's break down the three points asked in the question.
1. Electronic Configuration
Lanthanoids (Ce to Lu, Z = 58–71): The general configuration is . The 4f subshell fills regularly, with a few exceptions carrying a single 5d electron in NCERT's own table (Ce, Gd and Lu — Gd's preserving the stable half-filled , Lu's accompanying the filled ). The 4f orbitals are deeply buried inside the core, so they barely participate in bonding.
Actinoids (Th to Lr, Z = 90–103): The general configuration is . Here, the picture is messier. The 5f, 6d, and 7s orbitals are much closer in energy. This leads to:
- Greater irregularity in filling. For example, Th () has (no 5f electron), Pa has , and U has .
- Electrons can "jump" between 5f and 6d orbitals with small energy changes, leading to multiple possible ground-state configurations for the same element.
A common mistake is to assume the 5f series fills as neatly as the 4f series. It does not. The 5f–6d–7s energy overlap means you must check the actual configuration for each actinoid; there is no simple "one electron per element" rule.
2. Oxidation States
Lanthanoids: The dominant oxidation state is +3 for all elements. A few show +2 (Eu, Yb) or +4 (Ce, Tb) but these are less stable and require special conditions. The +3 state is so stable because removing the two 6s electrons and one 4f electron leaves a configuration that is either half-filled, full, or empty — but even when it isn't, the 4f electrons are too tightly bound to be easily removed further.
Actinoids: Here, the story is dramatically different. The 5f electrons are more loosely held, so multiple oxidation states are common, especially for the early actinoids.
| Element | Common Oxidation States |
|---|---|
| Th | +4 (only) |
| Pa | +4, +5 |
| U | +3, +4, +5, +6 |
| Np | +3, +4, +5, +6, +7 |
| Pu | +3, +4, +5, +6, +7 |
| Am | +3, +4, +5, +6 |
| Cm onwards | +3 (dominant) |
Notice that uranium in its +6 state (as , the uranyl ion) is the most common form in nature. Plutonium can exist in four oxidation states simultaneously in the same solution — a unique chemical behaviour.
The key insight: early actinoids (up to Am) can use 5f, 6d, and 7s electrons for bonding, giving high oxidation states like +6 and +7. Later actinoids (Cm onward) have the 5f subshell half-filled or more, which stabilises the +3 state, making them more lanthanoid-like.
3. Chemical Reactivity …
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