Catalytic behavior
Variable oxidation states + ability to form complexes → catalysis. V₂O₅ (contact process), Fe (Haber), Ni (hydrogenation), TiCl₃ (Ziegler-Natta).
-- NCERT Class 12 Chemistry, Ch. 4, p. 14Transition metals act as catalysts in many industrial and biological reactions — and NEET asks about the why, not just the what. The core fact is straightforward: d-block elements exhibit catalytic behaviour because of (a) variable oxidation states allowing intermediate formation with reactants, and (b) large surface area in finely divided form (NCERT Class 12 Chemistry Chapter 4, page 14).
The mechanism link: A catalyst provides an alternative reaction pathway of lower activation energy. Transition metals achieve this by forming short-lived intermediates — cycling between oxidation states during the reaction and returning to the original state at the end. Example: Fe³⁺/Fe²⁺ in the Contact process; V₂O₅ cycling between V⁵⁺ and V⁴⁺ in sulfuric acid manufacture.
What NEET actually tests:
Watch-out: Do not confuse "variable oxidation states" with "high oxidation states." Zinc (+2 only) and scandium (+3 only) are poor catalysts precisely because they lack multiple accessible oxidation states — yet both are d-block elements. NEET uses this distinction as a distractor.
Select an option to see the explanation. Wrong answers show why your choice was tempting — and name the exact trap it exploits.
Which property of transition metals is primarily responsible for their catalytic behaviour?
V₂O₅ is used as a catalyst in the Contact process. During catalysis, vanadium cycles between which oxidation states?
Which of the following d-block elements is a poor catalyst due to lack of variable oxidation states?
Finely divided iron is used in the Haber process rather than a large iron block because:
Which of the following correctly explains why scandium (Sc) is not commonly used as a catalyst?
In a catalysed reaction, the transition metal catalyst:
Among MnO₂, ZnO, Fe₂O₃, and CuO, which is commonly used as a catalyst for decomposition of KClO₃?
A student claims: "All d-block elements are good catalysts." Which pair of elements best disproves this claim?
Given
- V₂O₅: vanadium in +5 oxidation state - ZnO: zinc in +2 oxidation state - Reaction catalysed: 2SO₂ + O₂ → 2SO₃ (Contact process)
Required
Identify the property enabling V₂O₅ to act as a catalyst and explain why ZnO fails.
Concept
Catalytic behaviour in transition metals requires variable oxidation states to form intermediates with reactants, creating an alternative low-energy pathway.
Formula
No numerical formula required — this is a conceptual application of the variable-oxidation-state criterion.
Substitution / Application
- Vanadium: accessible oxidation states include +5, +4, +3, +2. In the Contact process, V⁵⁺ is reduced to V⁴⁺ by SO₂ (forming the intermediate), then reoxidised by O₂ back to V⁵⁺. - Zinc: only stable oxidation state is +2 (d¹⁰ configuration). Cannot be reduced or oxidised under Contact process conditions to form an intermediate.
Analysis
V₂O₅ cycles: V⁵⁺ + SO₂ → V⁴⁺ + SO₃, then V⁴⁺ + ½O₂ → V⁵⁺. The catalyst is regenerated. ZnO cannot undergo this cycling because Zn²⁺ has no accessible lower or higher oxidation state under these conditions.
Final answer
V₂O₅ is effective because vanadium has multiple accessible oxidation states (+4/+5 cycling), enabling intermediate formation and catalyst regeneration. ZnO fails because Zn²⁺ (d¹⁰) has only one stable oxidation state (+2) — the fundamental requirement for catalytic activity (variable oxidation states) is absent.
Common trap
Students may argue "ZnO is a d-block oxide, so it should catalyse reactions." The trap is equating "d-block membership" with "catalytic ability." The criterion is not membership in the d-block but the availability of multiple oxidation states for intermediate cycling.
Similar NEET-style question
"Among TiO₂, V₂O₅, ZnO, and CuO, which oxide(s) can act as effective catalysts for redox reactions and why?" ---
Variable oxidation states + ability to form complexes → catalysis. V₂O₅ (contact process), Fe (Haber), Ni (hydrogenation), TiCl₃ (Ziegler-Natta).
-- NCERT Class 12 Chemistry, Ch. 4, p. 14Magnetic moment from n unpaired electrons. 1 unpaired: 1.73 BM; 5: 5.92 BM.
| Symbol | Quantity | SI Unit |
|---|---|---|
| n | unpaired electrons | - |
| mu | magnetic moment | Bohr magneton |
Predicts paramagnetic moment of d-block ion. n unpaired electrons in d-orbitals.
| Symbol | Quantity | SI Unit |
|---|---|---|
| n | unpaired electrons | - |
| mu | magnetic moment | BM |
Catalogues common stable oxidation states across first-row transition metals.
| Symbol | Quantity | SI Unit |
|---|---|---|
| OS | oxidation state | - |
These are the exact patterns that cause wrong answers in NEET. Each trap includes when it triggers and how to avoid it.
Category: Inorganic Exception
Student assumes Mn²⁺ is the product regardless of medium. Acidic: → Mn²⁺ (5e⁻). Neutral/weakly basic: → MnO₂ (3e⁻). Strongly basic: → MnO₄²⁻ (1e⁻).
Question gives KMnO4 oxidation in unspecified or specific medium.
Always check medium. In acidic: Mn(+7) → Mn(+2). In neutral: → Mn(+4) (MnO₂). In basic: → Mn(+6) (manganate). The number of electrons (n) in Nernst calculations depends accordingly.
Root cause: concept gap
Acidic: → Mn²⁺ (5e⁻). Neutral/weakly basic: → MnO₂ (3e⁻). Strongly basic: → MnO₄²⁻ (1e⁻).
Root cause: concept gap
Lanthanoid contraction (imperfect 4f shielding) makes 5d elements similar in size to 4d. Zr/Hf, Nb/Ta, Mo/W have nearly identical chemistry.
10 questions from NEET 2021, 2022, 2023, 2024, 2025. Answers verified against NTA official keys.
The correct order of decreasing basic strength of the given amines is:
The pair of lanthanoid ions which are diamagnetic is
Which one of the following statements is correct?
Gadolinium has a low value of third ionisation enthalpy because of
Tritium, a radioactive isotope of hydrogen, emits which of the following particles? (β–)
Recurring question shapes from past papers. Each pattern shows why wrong options look tempting.
uses acidic formula in basic medium
Assumes Mn²⁺ regardless of medium
predicts large difference due to period shift
Expects 5d to be much larger than 4d
misses d0 d10 stability
Doesn't account for closed-shell stability
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