NEET Chemistry Coordination Compounds 2027 — Werner Theory, CFT, Isomerism and 40 Practice MCQs | Neet Gurukul

NEET Chemistry Coordination Compounds 2027 — Werner Theory, CFT, Isomerism and 40 Practice MCQs

NEET UG preparation medical entrance study material

Last Updated: 11 May 2026

Coordination Compounds is among the highest-yield NEET 2027 chapters in Inorganic Chemistry — 3-4 questions worth 12-16 marks. NCERT Class 12 Ch. 9 has driven 18 NEET questions in the last 5 years, including 4 in NEET 2026.

Werner’s Coordination Theory (1893)

  1. A metal exhibits two types of valencies — primary (ionisable) and secondary (non-ionisable).
  2. Primary valencies are satisfied by negative ions; secondary valencies by ligands.
  3. Every metal has a fixed coordination number (secondary valency).
  4. Secondary valencies are directional → gives specific geometry.

Key Terminology

  • Coordination Sphere: [M(L)n]; written inside square brackets.
  • Ligand: Lewis base donating electron pair(s).
  • Denticity: number of donor atoms — Monodentate (Cl-, NH3), Bidentate (en, ox), Polydentate (EDTA — hexadentate).
  • Chelate: ring-forming polydentate ligand.
  • Ambidentate: can bind through different atoms — SCN- (S or N), NO2- (N or O).

IUPAC Nomenclature Rules

  1. Cation named first.
  2. Within complex: ligands alphabetically (ignore Greek prefix).
  3. Prefixes: di-, tri-, tetra- (mono/poly for complex names use bis-, tris-, tetrakis-).
  4. Metal oxidation state in Roman numerals in parentheses.
  5. For anionic complex, metal name ends in ‘-ate’ (e.g., ferrate, cuprate).

Isomerism in Coordination Compounds

Type Example
Ionisation [Co(NH3)5Br]SO4 vs [Co(NH3)5SO4]Br
Hydrate [Cr(H2O)6]Cl3 vs [Cr(H2O)5Cl]Cl2·H2O
Linkage [Co(NH3)5(NO2)]2+ vs [Co(NH3)5(ONO)]2+
Coordination [Co(NH3)6][Cr(CN)6] vs [Cr(NH3)6][Co(CN)6]
Geometrical (cis-trans) [Pt(NH3)2Cl2]
Optical [Co(en)3]3+

Valence Bond Theory (VBT)

  • Inner orbital complex: (n-1)d2sp3 — diamagnetic, low spin (strong field ligands).
  • Outer orbital complex: sp3d2 — paramagnetic, high spin (weak field ligands).
  • Ligand strength order (Spectrochemical series): I- < Br- < Cl- < F- < OH- < H2O < NH3 < en < CN- < CO.

Crystal Field Theory (CFT) Essentials

  • Octahedral splitting: t2g (lower, 3 orbitals) and eg (higher, 2 orbitals). Δ_o = crystal field splitting energy.
  • Tetrahedral splitting: e (lower, 2) and t2 (higher, 3); Δ_t ≈ 4/9 × Δ_o.
  • CFSE (Crystal Field Stabilisation Energy): = (-0.4 × t2g electrons + 0.6 × eg electrons) × Δ_o.
  • Colour: arises from d-d transitions; observed colour is complementary to absorbed.

Important Complexes (NCERT Examples)

  • [Fe(CN)6]4-: d2sp3, diamagnetic, hexacyanoferrate(II), used in K4[Fe(CN)6].
  • [Ni(CO)4]: sp3, tetrahedral, diamagnetic, Mond’s process.
  • [Cu(NH3)4]2+: dsp2, square planar, paramagnetic.
  • cis-[PtCl2(NH3)2]: anti-cancer drug (Cisplatin).
  • EDTA-Ca2+: water hardness estimation.

Internal Links

FAQ

Average questions from this chapter in NEET?

3-4 questions worth 12-16 marks.

Most-asked subtopic?

Isomerism (linkage + geometrical) — at least 1 question every year.

VBT or CFT — which is more tested?

Both. VBT (hybridisation + magnetic moment) and CFT (splitting + colour) are equally probable.

Practice Quiz

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