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Coordination Compounds

Coordination CompoundsNEET Chemistry · Class 12 · NCERT Chapter 5

2 interactive concept widgets for Coordination Compounds. Drag any slider, change any number, and watch the formula and the answer update live. Built so you understand how each NEET problem actually works, not just the final number.

IUPAC naming flashcard practice

See a coordination compound formula, recall the IUPAC name, then reveal to check. Each card explains the key naming rule, oxidation state, and coordination number.

IUPAC nomenclature

Coordination compound naming: flashcard practice

See the formula, recall the IUPAC name, then reveal to check. Each card shows the name, oxidation state, coordination number, and the key naming rule that applies.

Card 1 of 10

Formula

[Co(NH₃)₆]³⁺

What is the IUPAC name of this coordination compound?

Try this

  • The naming rule: ligands first (alphabetical), then metal with oxidation state. If the complex is an anion, the metal name gets "-ate".
  • Card 5 ([Cu(en)₂]²⁺) uses "bis()" not "di-" because "en" is a complex ligand name. Remember: bi/bis for complex names.
  • Card 9 ([Pt(NH₃)₂Cl₂]) is cisplatin (cis form) — a famous anticancer drug. The naming itself is a frequent NEET question.

Crystal field splitting diagram

Choose geometry (octahedral or tetrahedral), set d-electron count, and toggle field strength to see orbital filling, spin state, magnetic moment, and crystal field stabilisation energy.

Crystal Field Theory

Crystal field splitting: orbital filling and CFSE

Choose geometry (octahedral or tetrahedral), set d-electron count, and toggle field strength to see orbital filling, spin state, magnetic moment, and crystal field stabilisation energy.

Octahedral field: 5 d-orbitals split into t₂g (×3) and eɡ (×2)

Higher energy (destabilised)

↑↓

eɡ (+0.6Δo each)

Lower energy (stabilised)

↑↓
↑↓

t₂g (-0.4Δo each)

Unpaired electrons

1

Magnetic moment

1.73 BM (paramagnetic)

CFSE

-0.4Δo

Spin type

High spin

Try this

  • d⁶ octahedral is the most tested case: weak field gives 4 unpaired (high spin, Fe²⁺ with H₂O); strong field gives 0 unpaired (low spin, Fe²⁺ with CN⁻).
  • Tetrahedral complexes are almost always high spin because Δt = 4/9 Δo is too small to overcome pairing energy.
  • CFSE is maximum for d³ and d⁸ (octahedral). This explains why Cr³⁺ and Ni²⁺ form very stable octahedral complexes.

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