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Class 12 · Chemistry · Chapter 5

Coordination Compounds: Class 12 Important Questions with Answers

72 important questions for Class 12 Chemistry Chapter 5, Coordination Compounds, the way they come in the board exam: MCQs, assertion–reason, case-based and short and long answer questions, with answers. Taken from our Class 12 Chemistry notes for 2026-27.

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Jump to: Practice set: test yourself20 MCQsAssertion–ReasonAnswers to the practice set

Practice set: test yourself

Try every question before looking at the answers below. 64 or more out of 80 means you are ready for the board.

A. Fill in the blanks (1 mark each)

  1. The CN of Co in [Co(en)₂Cl₂]⁺ is ______.
  2. NO₂⁻ is an ______ ligand.
  3. Δt = ______ Δo.
  4. [Ni(CN)₄]²⁻ is ______ in shape.
  5. Secondary valence equals the ______.
  6. Wilkinson's catalyst contains ______.
  7. cis-platin is used to treat ______.
  8. The strongest field ligand in the series is ______.

B. True or false? (1 mark each)

  1. Mohr's salt is a complex.
  2. Tetrahedral complexes show geometrical isomerism.
  3. [Fe(CN)₆]³⁻ is an inner orbital complex.
  4. Primary valences are non-ionisable.
  5. trans-[CoCl₂(en)₂]⁺ is optically active.
  6. EDTA titration measures the hardness of water.
  7. CO forms synergic bonds with metals.
  8. [CoF₆]³⁻ is low spin.

C. Very short answer (1 mark each)

  1. Define a ligand.
  2. What is a chelate?
  3. Name [Ni(CO)₄].
  4. Formula of potassium hexacyanidoferrate(II).
  5. Oxidation state of Cu in [Cu(CN)₄]³⁻.
  6. What is linkage isomerism?
  7. Why is CO a strong ligand?
  8. Define pairing energy.
  9. Give one biological complex.
  10. What is a homoleptic complex?

D. Short answer I (2 marks each)

  1. Name: (a) [Co(NH₃)₅Cl]Cl₂ (b) K₂[Ni(CN)₄].
  2. Write the formulae: (a) tetraamminecopper(II) sulphate (b) potassium tetrachloridoplatinate(II).
  3. Moles of AgCl from CoCl₃·5NH₃? Structure?
  4. Draw cis and trans [Pt(NH₃)₂Cl₂].
  5. Calculate μ for [Fe(H₂O)₆]³⁺.
  6. Why is [Ti(H₂O)₆]³⁺ violet?
  7. Give the d⁶ configurations for Δo > P and Δo < P.
  8. Distinguish inner and outer orbital complexes.
My score (fill in after checking the answers)
SectionA /8B /8C /10D /16E /18F /20G (bonus)Total /80
My marks

Rough work

E. Short answer II (3 marks each)

  1. Explain the hybridisation, shape and magnetism of [Co(NH₃)₆]³⁺ (VBT).
  2. Draw the octahedral splitting diagram and explain Δo.
  3. Explain linkage, ionisation and coordination isomerism with one example each.
  4. Why is [NiCl₄]²⁻ paramagnetic but [Ni(CN)₄]²⁻ diamagnetic?
  5. Write IUPAC names: [Cr(en)₃]Cl₃, [Pt(NH₃)₄][PtCl₄], K₃[Al(C₂O₄)₃].
  6. Give three applications of coordination compounds.

F. Long answer (5 marks each)

  1. (a) State the postulates of Werner's theory. (b) CoCl₃·4NH₃ gives 1 mol AgCl. Write its structure and name. (c) How many geometrical isomers does it have?
  2. (a) Compare VBT and CFT for [Fe(CN)₆]³⁻ and [FeF₆]³⁻. (b) Explain why tetrahedral complexes are high spin. (c) Arrange [Co(H₂O)₆]³⁺, [Co(NH₃)₆]³⁺, [Co(CN)₆]³⁻ by Δo.

G. HOTS (higher-order thinking)

  1. Why is [Co(NH₃)₆]³⁺ yellow-orange but [CoF₆]³⁻ blue?
  2. Why does [Cu(NH₃)₄]²⁺ form a deep blue colour from pale blue [Cu(H₂O)₄]²⁺?
  3. Why can't [Ni(NH₃)₆]²⁺ be an inner orbital complex?
  4. Why is the cis isomer of [Pt(en)₂Cl₂]²⁺ optically active but not the trans?

20 MCQs

  1. CN of Fe in [Fe(C₂O₄)₃]³⁻
    (a) 3 (b) 4 (c) 6 (d) 9
  2. Ambidentate ligand
    (a) SCN⁻ (b) NH₃ (c) en (d) H₂O
  3. Hybridisation of [Ni(CN)₄]²⁻
    (a) sp³ (b) sp³d² (c) d²sp³ (d) dsp²
  4. Unpaired electrons in [CoF₆]³⁻
    (a) 0 (b) 4 (c) 2 (d) 5
  5. Strongest field ligand
    (a) H₂O (b) CO (c) Cl⁻ (d) NH₃
  6. Oxidation state of Pt in [PtCl₂(en)₂]²⁺
    (a) +2 (b) 0 (c) +6 (d) +4
  7. Moles of AgCl from [Co(NH₃)₅Cl]Cl₂
    (a) 2 (b) 1 (c) 3 (d) 0
  8. Optically active
    (a) trans-[CoCl₂(en)₂]⁺ (b) [Pt(NH₃)₂Cl₂] (c) [Co(en)₃]³⁺ (d) [Ni(CO)₄]
  9. Geometry of [Ni(CO)₄]
    (a) square planar (b) linear (c) octahedral (d) tetrahedral
  10. Highest conductivity
    (a) [Co(NH₃)₃Cl₃] (b) [Co(NH₃)₆]Cl₃ (c) [Co(NH₃)₄Cl₂]Cl (d) [Co(NH₃)₅Cl]Cl₂
  11. Configuration of d⁶ with Δo > P
    (a) t₂g⁴e_g² (b) t₂g³e_g³ (c) t₂g⁶ (d) t₂g⁵e_g¹
  12. Chelating ligand
    (a) C₂O₄²⁻ (b) Cl⁻ (c) NH₃ (d) CN⁻
  13. Used against lead poisoning
    (a) cis-platin (b) EDTA (c) DMG (d) en
  14. [Co(NH₃)₅NO₂]²⁺ and [Co(NH₃)₅ONO]²⁺ are
    (a) ionisation (b) coordination (c) linkage (d) optical isomers
  15. Name of [Fe(CN)₆]³⁻
    (a) hexacyanidoiron(III) (b) ferricyanide(II) (c) hexacyanoiron(II) (d) hexacyanidoferrate(III)
  16. Colourless complex
    (a) [Zn(H₂O)₆]²⁺ (b) [Ti(H₂O)₆]³⁺ (c) [Cu(H₂O)₄]²⁺ (d) [Ni(H₂O)₆]²⁺
  17. Geometrical isomers of [Co(NH₃)₃Cl₃]
    (a) 2 (b) 1 (c) 3 (d) 4
  18. e_g orbitals in an octahedral field
    (a) dxy, dyz (b) all five (c) dxz, dyz (d) d(x²−y²), d(z²)
  19. Mond process refines
    (a) Fe (b) Ni (c) Cu (d) Ag
  20. μ of [Mn(CN)₆]⁴⁻
    (a) 5.92 (b) 3.87 (c) 1.73 (d) 0

1 (c) · 2 (a) · 3 (d) · 4 (b) · 5 (b) · 6 (d) · 7 (a) · 8 (c) · 9 (d) · 10 (b) · 11 (c) · 12 (a) · 13 (b) · 14 (c) · 15 (d) · 16 (a) · 17 (a) · 18 (d) · 19 (b) · 20 (c)

Assertion–Reason (6)

(a) Both true, R explains A. (b) Both true, R does not explain A. (c) A true, R false. (d) A false, R true.

  1. A: [Ni(CO)₄] is diamagnetic. R: CO pairs the electrons of Ni.
  2. A: Tetrahedral complexes are generally high spin. R: Δt is smaller than the pairing energy.
  3. A: [Co(NH₃)₃Cl₃] gives 3 mol AgCl. R: It has three Cl atoms.
  4. A: [Fe(C₂O₄)₃]³⁻ is more stable than [FeCl₆]³⁻. R: Oxalate forms chelate rings.
  5. A: Cu²⁺ salts are coloured. R: Cu²⁺ has a d⁹ configuration.
  6. A: CO is a weak field ligand. R: CO forms σ and π bonds with the metal.

Key: 1 (a) · 2 (a) · 3 (d) · 4 (a) · 5 (a) · 6 (d)

Answers to the practice set

A. 1. 6 2. ambidentate 3. 4/9 4. square planar 5. coordination number 6. rhodium 7. cancer 8. CO

B. 1. F (double salt) 2. F 3. T 4. F 5. F 6. T 7. T 8. F

C. 1. an ion or molecule donating a lone pair to the metal 2. a ring complex of a di/polydentate ligand 3. tetracarbonylnickel(0) 4. K₄[Fe(CN)₆] 5. +1 6. ambidentate ligand bound through different atoms 7. σ donation + π back-bonding 8. energy needed to pair two electrons in one orbital 9. haemoglobin 10. only one kind of ligand

D. 1. (a) pentaamminechloridocobalt(III) chloride (b) potassium tetracyanidonickelate(II) 2. (a) [Cu(NH₃)₄]SO₄ (b) K₂[PtCl₄] 3. 2 mol; [Co(NH₃)₅Cl]Cl₂ 4. p. 4 5. d⁵ high spin: √35 = 5.92 BM 6. p. 6 7. t₂g⁶ and t₂g⁴e_g² 8. p. 5

Answers to E, F, G, case study (short, long and HOTS answers, step by step) are in the notes pack

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