Coordination CompoundsJEE Main

Build a complex — charge, CN & geometry — interactive Chemistry simulation for IIT-JEE.

Concept

A coordination compound is a central metal ion holding ligands by coordinate (dative) bonds inside square brackets. The coordination number counts bonded atoms — bidentate ligands like en bite twice. Complex charge = metal oxidation state + sum of ligand charges; counter-ions outside the bracket balance it.

Key formula

charge=OSmetal+Σ(ligand charges),CN=Σ(denticity)\text{charge} = OS_{metal} + \Sigma(\text{ligand charges}), \qquad CN = \Sigma(\text{denticity})

Derivation

Werner's insight: two kinds of valence — primary (oxidation state, satisfied by anions anywhere) and secondary (CN, satisfied only inside the sphere).

Only ionisable (outside) chloride precipitates with AgNO₃: [Co(NH₃)₆]Cl₃ gives 3 AgCl, [Co(NH₃)₅Cl]Cl₂ gives 2 — the classic experiment distinguishing isomers.

Scenarios to explore

  • Coordination Compounds — Build a complex — charge, coordination number & geometry.

Real-world applications

  • Haemoglobin (Fe–porphyrin), chlorophyll (Mg), vitamin B₁₂ (Co).
  • cis-platin [PtCl₂(NH₃)₂] chemotherapy.
  • EDTA chelation therapy & water softening.

JEE exam tips

  • Naming order: ligands alphabetically, then metal (with -ate suffix if the complex is anionic).
  • AgNO₃ / conductivity tests count IONISABLE ions — inside-sphere ligands don't show.
  • Chelate effect: ring-forming ligands give extra entropy-driven stability.

Common mistakes

  • Counting en as ONE toward CN — bidentate counts two.
  • Confusing coordination number with the number of ligands.
  • Oxidation state vs complex charge mix-ups.

Exam traps to avoid

  • CN 4 geometry: Ni²⁺/Pt²⁺ (strong field, d⁸) go square planar; Zn²⁺ tetrahedral.
  • [Co(NH₃)₄Cl₂]⁺ has cis/trans isomers — geometry drives isomer counting questions.