Class 12 Chemistry

Chapter 4 — The d- and f-Block Elements

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Overview

Summary

Class 12 Chemistry Chapter 4 covers the d- and f-block elements — the transition metals (Groups 3–12) and the inner transition metals (lanthanoids and actinoids) — explaining their electronic configurations, variable oxidation states, magnetic behaviour, coloured ions, catalytic properties, and key compounds such as K₂Cr₂O₇ and KMnO₄.

The d-block (Groups 3–12) and f-block elements occupy the middle and bottom sections of the periodic table. Transition metals are defined as metals with an incomplete d subshell in the neutral atom or its ions; zinc, cadmium and mercury are excluded. These elements show variable oxidation states, paramagnetism, formation of coloured ions and complex compounds, catalytic activity, interstitial compound formation, and alloy formation. The f-block comprises two series: lanthanoids (4f, Ce–Lu) and actinoids (5f, Th–Lr). Lanthanoid contraction causes the second and third d-series to have nearly identical radii. Important compounds include K₂Cr₂O₇ and KMnO₄, both strong oxidising agents with wide industrial and analytical uses.

Essentials

Key points & formulas

  1. 01Transition metals are in Groups 3–12; their d orbitals are progressively filled across four series (3d, 4d, 5d, 6d). Zn, Cd and Hg are not true transition metals because their d orbitals are completely filled in ground state and common oxidation states.
  2. 02Variable oxidation states arise from incomplete d-orbital filling; manganese shows the widest range (+2 to +7). Oxidation states in d-block elements differ by one unit, unlike p-block elements where they differ by two.
  3. 03Transition metals are paramagnetic due to unpaired d electrons; magnetic moment is calculated using the spin-only formula µ = √(n(n+2)) BM, where n is the number of unpaired electrons.
  4. 04Coloured ions result from d–d electronic transitions when energy absorbed falls in the visible region; ions with completely filled or empty d orbitals (e.g., Sc³⁺, Zn²⁺) are colourless.
  5. 05Lanthanoid contraction — the steady decrease in atomic and ionic radii from La to Lu — causes the 5d elements (e.g., Hf, 159 pm) to have almost identical radii to their 4d counterparts (e.g., Zr, 160 pm), making their separation in nature difficult.
  6. 06Actinoids (Th–Lr) exhibit a wider range of oxidation states than lanthanoids because the 5f, 6d and 7s energy levels are comparable; all actinoids are radioactive, with heavier members having very short half-lives.
Questions

Frequently asked questions

01

What is lanthanoid contraction and what are its consequences?

Lanthanoid contraction is the gradual decrease in atomic and ionic radii of the lanthanoid elements from lanthanum (La) to lutetium (Lu) due to poor shielding of one 4f electron by another as nuclear charge increases. Its main consequence is that the 5d transition series elements have nearly the same atomic radii as the corresponding 4d elements (e.g., Zr 160 pm and Hf 159 pm), causing them to co-occur in nature and making their separation very difficult.

02

How is potassium permanganate (KMnO₄) prepared and what are its oxidising reactions in acidic solution?

KMnO₄ is prepared commercially by alkaline oxidative fusion of MnO₂ (pyrolusite ore) with KOH in the presence of air or KNO₃ to form green K₂MnO₄ (manganate), followed by electrolytic oxidation of manganate in alkaline solution to permanganate. In acidic solution the half-reaction is: MnO₄⁻ + 8H⁺ + 5e⁻ → Mn²⁺ + 4H₂O (Eº = +1.52 V). It oxidises Fe²⁺ to Fe³⁺, iodides to I₂, oxalate to CO₂, and nitrites to nitrates.

03

Why do transition metals show variable oxidation states while most main-group metals do not?

Transition metals have partially filled (n–1)d orbitals with small energy differences between them and the ns orbitals, so varying numbers of electrons can be lost or shared without a prohibitive energy cost. Their oxidation states therefore differ by one unit (e.g., V²⁺, V³⁺, V⁴⁺, V⁵⁺), whereas non-transition elements typically show oxidation states differing by two units due to the inert pair effect and larger energy gaps between subshells.

04

Is the NCERT Class 12 Chemistry Chapter 4 PDF free to download?

Yes, the NCERT Class 12 Chemistry Part I Chapter 4 PDF is completely free to download on cbseprepmaster.com.

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This is the complete Chemistry Part I Chapter 4 as published by NCERT — every diagram, solved example, and exercise included, free. Browse all CBSE Class 12 textbooks.

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