Class 12 Chemistry

Chapter 5 — Coordination Compounds

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Overview

Summary

Chapter 5 of the Class 12 Chemistry NCERT textbook, "Coordination Compounds", covers Werner's theory, nomenclature, isomerism, and bonding theories (VBT and CFT) for complexes where a central metal ion is bound to ligands in a definite geometric arrangement.

  • Werner's picture of coordinationThe chapter builds on Werner's insight that metal ions carry both primary (ionisable) and secondary (non-ionisable) valences, with the secondary valence fixing the coordination number and hence the octahedral, tetrahedral or square-planar shape of a complex.
  • Ligands, naming and isomerismIt organises ligands by how many donor atoms they use and lays out IUPAC naming rules, then surveys the many ways complexes can differ in structure — geometric, optical, linkage, coordination, ionisation and solvate isomerism.
  • Bonding theories that explain colour and magnetismValence Bond Theory and Crystal Field Theory are used to account for shape, colour and magnetic behaviour, with CFT's d-orbital splitting explaining low- versus high-spin complexes and the colours seen in transition-metal solutions.
  • Biological and practical importanceThe chapter connects the theory to life and industry — chlorophyll, haemoglobin and vitamin B12 are all coordination compounds, and complexes serve in metallurgy, catalysis and medicine such as the anticancer drug cisplatin.
Essentials

Key points & formulas

  1. 01Werner's theory distinguishes primary (ionisable) valence and secondary (non-ionisable) valence; the secondary valence equals the coordination number and determines geometry (octahedral, tetrahedral, square planar).
  2. 02Ligands are classified by denticity: unidentate (Cl⁻, NH₃), didentate (ethane-1,2-diamine, C₂O₄²⁻), polydentate (EDTA⁴⁻ is hexadentate), and ambidentate (NO₂⁻, SCN⁻ can bind through either of two atoms).
  3. 03Isomerism types include geometric (cis/trans, fac/mer), optical (non-superimposable mirror images in octahedral complexes with didentate ligands), linkage, coordination, ionisation, and solvate isomerism.
  4. 04Crystal Field Theory explains colour via d-d electronic transitions and magnetic behaviour via d-orbital splitting (Δo for octahedral, Δt = 4/9 Δo for tetrahedral); strong-field ligands cause low-spin and weak-field ligands cause high-spin configurations.
  5. 05Metal carbonyls exhibit synergic bonding: ligand-to-metal σ donation plus metal-to-ligand π back-donation into the CO antibonding π* orbital, stabilising the M–C bond.
  6. 06Biological significance: chlorophyll (Mg), haemoglobin (Fe), and vitamin B12 (Co) are coordination compounds; medicinal uses include cisplatin (anticancer), EDTA (lead poisoning), and chelate therapy for toxic metal removal.
Questions

Frequently asked questions

01

What are the main postulates of Werner's theory of coordination compounds?

Werner proposed that metal ions have two types of valences: primary valences (ionisable, satisfied by negative ions) and secondary valences (non-ionisable, satisfied by neutral molecules or negative ions). The secondary valence equals the coordination number, which is fixed for a metal, and determines the spatial (geometric) arrangement of ligands around the central atom, forming shapes such as octahedral, tetrahedral, or square planar.

02

What is the spectrochemical series and how does it affect complex properties?

The spectrochemical series is an experimentally determined order of ligands based on their crystal field splitting ability: I⁻ < Br⁻ < SCN⁻ < Cl⁻ < S²⁻ < F⁻ < OH⁻ < C₂O₄²⁻ < H₂O < NCS⁻ < EDTA⁴⁻ < NH₃ < en < CN⁻ < CO. Strong-field ligands (like CN⁻ and CO) produce large Δo, causing electron pairing and low-spin complexes, while weak-field ligands (like F⁻ and Cl⁻) result in small Δo and high-spin complexes.

03

How does Crystal Field Theory explain the colour of coordination compounds?

In CFT, ligands split the d orbitals of the central metal ion into sets of different energy (t₂g and eɡ in octahedral complexes). When visible light of a specific wavelength is absorbed, an electron is promoted from the lower t₂g to the higher eɡ level (d-d transition). The colour observed is complementary to the absorbed wavelength. For example, [Ti(H₂O)₆]³⁺ absorbs blue-green light (~498 nm) and appears violet.

04

Is the NCERT Class 12 Chemistry Chapter 5 PDF free to download?

Yes, the NCERT Class 12 Chemistry Part I Chapter 5 (Coordination Compounds) PDF is completely free to download on cbseprepmaster.com.

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More chapters in Chemistry Part I

Read Chapter 5 of Chemistry Part I, the Class 12 Chemistry NCERT textbook (2026-27 edition), online for free: the complete chapter as published by NCERT with every diagram, solved example and exercise, with step-by-step solutions, answers and revision notes. Open the NCERT PDF above, or browse all CBSE Class 12 textbooks.

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