Q.Identify the following :
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🔒 Start your 14-day free trial to unlock the full solution →Concept understanding — Variable Oxidation States
Variable Oxidation States – The Intuition
Think of an atom as having a wallet with two compartments. In most elements, one compartment is much easier to open than the other — you can only take money from the shallow one, so the amount you can spend (the oxidation state) is fixed. For transition metals, both compartments are at nearly the same depth. You can reach into either, and you can take different combinations of notes from each. That is variable oxidation states in a nutshell.
Iron, for example, can lose two electrons to become Fe2+ or three to become Fe3+. Manganese can show +2, +3, +4, +6, and +7. This is not random — it follows a clear pattern rooted in energy.
The Precise Statement
Transition metals exhibit variable oxidation states because the (n−1)d and ns subshells have similar energies. Electrons can be removed from both subshells in different numbers, producing a range of stable positive oxidation states.
The key is similar energies. In main-group elements (like sodium or chlorine), the outermost ns and np electrons are far higher in energy than the inner core — you lose only the valence electrons, and the oxidation state is fixed. In transition metals, the (n−1)d orbital is not much lower than the ns orbital. Both are close enough that losing a few d electrons along with the s electrons costs comparable energy.
Why This Happens – The Energy Picture
For a transition metal like iron ([Ar]3d64s2), the 4s orbital is actually slightly lower in energy than the 3d when the atom is neutral. But once you start removing electrons, the energy ordering shifts. The first two electrons lost are from the 4s orbital (giving Fe2+). The next electron lost comes from the 3d orbital (giving Fe3+). Because the 3d and 4s are so close in energy, removing that third electron does not require a huge jump in energy — it is feasible.
The actual order of filling is 4s before 3d, but the order of removal is also 4s first. This is not a contradiction — it is a consequence of how orbital energies change as the nuclear charge increases.
The Pattern Across the Series
For the first transition series (Sc to Zn), the common oxidation states are:
| Element | Common oxidation states |
|---|---|
| Sc | +3 |
| Ti | +3, +4 |
| V | +2, +3, +4, +5 |
| Cr | +2, +3, +6 |
| Mn | +2, +3, +4, +6, +7 |
| Fe | +2, +3 |
| Co | +2, +3 |
| Ni | +2 |
| Cu | +1, +2 |
| Zn | +2 |
Notice the trend: the maximum oxidation state increases from Sc (+3) to Mn (+7), then decreases. The maximum possible oxidation state equals the total number of electrons in the (n−1)d and ns orbitals (the "group number" for many). Manganese, with 3d54s2, can lose all seven — giving MnO4− where Mn is +7. After manganese, the d orbitals become more stable (higher effective nuclear charge), and it becomes harder to remove all of them.
Stability and the Environment
Not all oxidation states are equally stable. The stability depends on:
- The medium: Cr3+ is stable in acidic solution, but Cr6+ (as chromate) is stable in alkaline medium.
- The ligand: Some oxidation states are stabilised by certain ligands (this is where coordination chemistry meets redox). …
The 3d-series element with the most oxidation states is the one at the middle with the most unpaired/available electrons, and the ~95% lanthanoid alloy that sparks is a well-known ferrocerium alloy. …
(i) Mn (oxidation states +2 to +7). (ii) Mischmetal.
Concept. Trends of transition and inner-transition metals — CBSE Class-12 the-d-and-f-block-elements.
(i) Manganese has the electronic configuration [Ar]3d54s2. Because it can use both the 4s and all five 3d electrons in bonding, it exhibits the widest range of oxidation states in the 3d series: +2, +3, +4, +5, +6 and +7.
…
- AP EAPCET 2025Set ap-2025-05-19-FN1 markMCQQ.Which one of the following oxidizes manganous salt to permanganate in aqueous solution ? (A) H2O2 (B) O2 (C) O3 (D) K2S2O8
›Reveal solutionSolution
Among the given oxidizers, only peroxodisulphate (K2S2O8) is strong enough to oxidize Mn2+ all the way up to MnO4− (permanganate) in aqueous solution.
Concept and Intuition
Peroxodisulphate ion, S2O82−, contains a peroxide linkage (−O−O−) and is one of the strongest known oxidizing agents in aqueous chemistry (E⊖=2.01V), even stronger than H2O2 and O3 in this context. It is well known (a standard NCERT-cited example) for oxidizing Mn2+ to MnO4− in the presence of a catalyst (typically Ag+), taking manganese from the +2 to the +7 oxidation state.
Step-by-Step Solution
- Manganous ion is Mn2+; permanganate is MnO4−, i.e. manganese in the +7 state — a large jump in oxidation state (+2→+7).
- This requires a very strong oxidizing agent.
- H2O2 and O2 are comparatively mild oxidizers in this context and don't achieve this specific conversion reliably. …
- AP EAPCET 2024Set eng-2024-05-20-FN1 markMCQQ.Which transition metal does not form 'MO' type oxide? (M= transition metal) (A) V (B) Cr (C) Mn (D) Sc
›Reveal solutionSolution
Sc has essentially only the +3 oxidation state, so unlike V, Cr, and Mn, it does not form a stable MO (+2) monoxide — answer (D).
Concept and Intuition
Transition metals show variable oxidation states because the energies of the (n−1)d and ns electrons are close, allowing several to be lost. However, scandium (electronic configuration [Ar]3d14s2) has only three electrons beyond the noble-gas core, and it overwhelmingly favours losing all three to attain the very stable Sc3+ ([Ar], noble-gas configuration). A Sc2+ state (which would be needed for an "ScO"-type oxide) is highly unstable and not realized as a common compound.
Step-by-Step Solution
- V (vanadium): shows +2, +3, +4, +5; VO (vanadium(II) oxide) is a known compound. ✓ forms MO.
- Cr (chromium): shows +2, +3, +6 (and others); CrO (chromium(II) oxide) exists, though less stable/prone to oxidation. ✓ forms MO.
- Mn (manganese): shows +2 through +7; MnO (manganese(II) oxide) is a common, stable compound. ✓ forms MO. …
- AP EAPCET 2023Set ap-2023-05-22-FN1 markMCQQ.Which of the following is/are correct? i. CrO3 is an acidic oxide ii. Mo(VI) and W (VI) are found to be more stable than Cr (VI) iii. All Cu (II) halides are known except iodide iv. The E⊖ value for Cr3+/Cr2+ is much more positive than Mn3+/Mn2+ (A) i, ii, iii only (B) iv only (C) ii, iv only (D) i, iii only
›Reveal solutionSolution
Three of the four statements about transition metal chemistry (CrO3 acidity, Mo/W(VI) stability, and the missing CuI2) are correct; only the claim about Cr3+/Cr2+ vs Mn3+/Mn2+ reduction potentials is false.
Concept and Intuition
This question tests several classic d-block facts: (i) high oxidation state metal oxides tend to be acidic (CrO3 dissolves in alkali forming chromate), (ii) down a transition metal group, higher oxidation states become more stable relative to the top member (so Mo(VI), W(VI) are more stable than Cr(VI)), (iii) Cu2+ oxidizes iodide ion to iodine, so instead of CuI2 you only ever isolate CuI (Cu in +1 state), and (iv) reduction potentials of M3+/M2+ couples relate to the relative stability of the +2 and +3 states — Mn3+ is a very strong oxidizer (large positive E∘) because Mn2+ (d5, half-filled, extra stable) resists further oxidation, whereas Cr3+ (d3) is quite stable making Cr3+/Cr2+ far less positive.
Step-by-Step Solution
- Statement i: CrO3 is a strongly acidic oxide (forms chromic acid with water) — true.
- Statement ii: Mo(VI) and W(VI) oxidation states are more stable than Cr(VI) (a strong oxidizer, easily reduced) — true.
- Statement iii: CuI2 does not exist because Cu2+ oxidizes I− to I2, giving CuI instead — all other Cu(II) halides (F, Cl, Br) are known — true. …
- AP EAPCET 2023Set ap-2023-05-23-AN1 markMCQQ.The decomposition products of [FeO4]2− are (A) Fe3O4, O2 (B) FeO, O2 (C) Fe2O3, O2 (D) FeO, Fe2O3
›Reveal solutionSolution
Ferrate(VI), [FeO4]2−, is a very strong oxidiser and unstable at the +6 oxidation state; it decomposes to iron(III) oxide and oxygen gas.
Concept and Intuition
Iron's very highest oxidation states (like +6 in ferrate) are strongly oxidising and thermodynamically unstable relative to iron's more common +2/+3 states. Ferrate ion, prepared by oxidising Fe(III) in strongly alkaline/oxidising conditions, spontaneously self-reduces over time — since it is one of the strongest known oxidisers, it tends to oxidise whatever is nearby (including water) while itself being reduced, releasing oxygen gas as a byproduct and settling into the far more stable Fe(III) oxide.
Step-by-Step Solution
- [FeO4]2− has iron in the unusually high +6 oxidation state — a strongly oxidising, kinetically fragile species.
- On decomposition, iron is reduced from +6 down to the far more stable +3 state, forming iron(III) oxide, Fe2O3. …
- AP EAPCET 2022Set ap-2022-07-12-FN1 markMCQQ.The unstable halide of the following is (A) VI2 (B) VBr2 (C) VCl2 (D) VF2
›Reveal solutionSolution
Tests the rule that fluoride stabilizes high metal oxidation states while iodide (and the heavier halides) stabilize low oxidation states — so among the vanadium(II) dihalides, the fluoride is the unstable one.
Concept and Intuition
Halide ions differ enormously in hardness/softness and polarizability. F− is small, hard, and forms very ionic, high-lattice-energy salts — this favours high, highly-charged cations (it is the anion that best stabilizes species like MnO4−-type high oxidation states or VF5). I−, by contrast, is large, soft, and polarizable, and forms more covalent bonds — it stabilizes low oxidation state metal centres, because a soft cation and a soft anion together give extra covalent/CFSE-type stabilization that a hard F− cannot supply. A textbook parallel: CuI is a very stable, insoluble solid, while CuF is essentially unknown/unstable and readily disproportionates (2Cu+→Cu+Cu2+).
Step-by-Step Solution
- All four halides in the options — VF2,VCl2,VBr2,VI2 — represent vanadium in the same low oxidation state, +2.
- For a low oxidation state metal ion, the anion that best stabilizes it is the softer, more polarizable halide (Cl, Br, I), because it supplies extra covalent character that offsets the low ionic charge. …
- AP EAPCET 2021Set eng-2021-08-20-FN1 markMCQQ.Which of the following is not arranged in the correct sequence? (A) MO,M2O3,MO2,M2O5 - Decreasing basic nature (B) Sc,V,Cr,Mn - Increasing number of oxidation states (C) d5,d3,d1,d4 - Increasing magnetic moment (D) Mn2+,Fe2+,Cr2+,Co2+ - decreasing stability
›Reveal solutionSolution
Among the four given trends, the "increasing magnetic moment" order for d5,d3,d1,d4 is not actually increasing once checked against real unpaired-electron counts — answer (C).
Concept and Intuition
Magnetic moment (spin-only) μ=n(n+2) BM depends directly on n = number of unpaired d-electrons. For common high-spin transition-metal configurations, n equals the superscript itself when ≤5 (d1→1 unpaired, d2→2, d3→3, d4→4 high spin, d5→5 high spin). So μ increases monotonically as n increases from d1 to d5.
Step-by-Step Solution
- List each option's unpaired-electron count for high-spin ions: d1=1, d3=3, d4=4, d5=5.
- Option (A): MO→M2O3→MO2→M2O5 correctly tracks decreasing basicity as the metal's oxidation number rises (higher charge increases the oxide's covalent/acidic character) — correct sequence.
- Option (B): Sc (mainly +3, few states) →V (+2 to +5) →Cr (+1 to +6) →Mn (+2 to +7) — the number of accessible oxidation states genuinely increases across this series, peaking at Mn — correct sequence.
- Option (C): the printed order is d5,d3,d1,d4, i.e. unpaired-electron counts 5, 3, 1, 4 in that order. This is NOT increasing (5→3 is a decrease). The true increasing order would be d1<d3<d4<d5. …
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