NEET Chemistry · Chapter-wise PYQs

Coordination Compounds NEET PYQs (2005–2026) with Solutions

Coordination Compounds has appeared in 22 of the 22 NEET and AIPMT papers from 2005 to 2026, with 67 questions in all: about 3.0 per paper on average. The last five papers (2022–2026) had 22 questions from it.

The most-asked topics are Bonding & Crystal Field Theory (23), Isomerism (10) and Werner Theory & Basic Concepts (9).

NEET MIND's syllabus map rates Coordination Compounds as high weightage: about 3 questions (12 marks) in a NEET paper.

Free account: 15 PYQs from Coordination Compounds with explanations and progress tracking. Premium unlocks all 67.

PYQs in this chapter
67
Papers it appeared in
22 of 22
Average per paper
3.0
NEET weightage
High

10 solved Coordination Compounds PYQs

Real NEET and AIPMT questions from this chapter, newest first. Try each one, then open the answer and the step-by-step explanation.

  1. Question 1 (NEET 2026)

    NEET 2026MediumOptical isomerism in octahedral complexes
    Given below are two statements: Statement-I : [Fe(ox)3]3−\mathrm{[Fe(ox)_3]^{3-}} is chiral. Statement-II : trans – [Cr(H2O)2(ox)2]−\mathrm{[Cr(H_2O)_2(ox)_2]^{-}} is chiral. (Given : oxH2=HOOC−COOH\mathrm{oxH_2 = HOOC-COOH}) In light of the above statements, choose the most appropriate answer from the options given below:
    1. Option A: Both Statement-I and Statement-II are correct
    2. Option B: Both Statement-I and Statement-II are incorrect
    3. Option C: Statement-I is correct but Statement-II is incorrect
    4. Option D: Statement-I is incorrect but Statement-II is correct
    Show answer & explanation

    Correct answer: (C) Statement-I is correct but Statement-II is incorrect

    Explanation

    Statement-I: [Fe(ox)3]3−\mathrm{[Fe(ox)_3]^{3-}} is an octahedral complex of the type [M(AA)3]\mathrm{[M(AA)_3]} with three bidentate oxalate ligands. It has no plane of symmetry and exists as two non-superimposable mirror images (d and l forms). So it is chiral, and Statement-I is correct. Statement-II: in trans-[Cr(H2O)2(ox)2]−\mathrm{[Cr(H_2O)_2(ox)_2]^{-}} the two oxalate ligands lie in one plane and the two water molecules are on opposite axial positions. The plane containing the oxalate ligands is a mirror plane, so the trans isomer is superimposable on its mirror image and is achiral. Only the cis isomer is optically active. Statement-II is incorrect. So the answer is option (C).

  2. Question 2 (NEET 2026)

    NEET 2026EasyDouble salts: potash alum
    In potash alum, the ratio of K+\mathrm{K^+} and SO42−\mathrm{SO_4^{2-}} ions is
    1. Option A: 1:21 : 2
    2. Option B: 2:12 : 1
    3. Option C: 2:32 : 3
    4. Option D: 3:23 : 2
    Show answer & explanation

    Correct answer: (A) 1:21 : 2

    Explanation

    Potash alum is the double salt KAl(SO4)2⋅12H2O\mathrm{KAl(SO_4)_2 \cdot 12H_2O}, also written K2SO4⋅Al2(SO4)3⋅24H2O\mathrm{K_2SO_4 \cdot Al_2(SO_4)_3 \cdot 24H_2O}. In water it dissociates completely into simple ions: KAl(SO4)2→K++Al3++2SO42−\mathrm{KAl(SO_4)_2 \rightarrow K^+ + Al^{3+} + 2SO_4^{2-}} Each formula unit gives 1 $\mathrm{K^+}forevery2for every 2\mathrm{SO_4^{2-}}ions,soions, so\mathrm{K^+ : SO_4^{2-}} = 1 : 2$, option (A).

  3. Question 3 (NEET 2026)

    NEET 2026MediumIsomerism
    Match List I with List II: Choose the correct answer from the options given below :
    1. Option A: A–III, B–I, C–II, D–IV
    2. Option B: A–I, B–III, C–II, D–IV
    3. Option C: A–II, B–IV, C–III, D–I
    4. Option D: A–III, B–I, C–IV, D–II
    Show answer & explanation

    Correct answer: (D) A–III, B–I, C–IV, D–II

    Explanation

    [Pt(NH₃)₂Cl₂] shows geometrical isomerism; [Co(en)₃]³⁺ shows optical isomerism; [Co(NH₃)₅NO₂]Cl₂ shows linkage isomerism; [Cr(H₂O)₆]Cl₃ shows solvate isomerism. Hence option (D) is correct.

  4. Question 4 (NEET 2026)

    NEET 2026EasySpectrochemical series of ligands
    According to crystal field theory, the correct order of ligands with respect to their decreasing order of field strength is
    1. Option A: CO>NH3>H2O>Cl−\mathrm{CO > NH_3 > H_2O > Cl^-}
    2. Option B: CO>H2O>NH3>Cl−\mathrm{CO > H_2O > NH_3 > Cl^-}
    3. Option C: Cl−>H2O>NH3>CO\mathrm{Cl^- > H_2O > NH_3 > CO}
    4. Option D: Cl−>NH3>H2O>CO\mathrm{Cl^- > NH_3 > H_2O > CO}
    Show answer & explanation

    Correct answer: (A) CO>NH3>H2O>Cl−\mathrm{CO > NH_3 > H_2O > Cl^-}

    Explanation

    The spectrochemical series (increasing field strength) from NCERT is: I−<Br−<SCN−<Cl−<S2−<F−<OH−<C2O42−<H2O<NCS−<edta4−<NH3<en<CN−<CO\mathrm{I^- < Br^- < SCN^- < Cl^- < S^{2-} < F^- < OH^- < C_2O_4^{2-} < H_2O < NCS^- < edta^{4-} < NH_3 < en < CN^- < CO} Taking the four given ligands in decreasing order of field strength: $\mathrm{CO > NH_3 > H_2O > Cl^-}$. So the answer is option (A).

  5. Question 5 (NEET 2026)

    NEET 2026EasyWerner Theory & Basic Concepts
    Which one of the following is an ambidentate ligand?
    1. Option A: Ethane-1,2-diamine
    2. Option B: Ethylenediaminetetraacetate ion
    3. Option C: Thiocyanate
    4. Option D: Oxalate
    Show answer & explanation

    Correct answer: (C) Thiocyanate

    Explanation

    Ambidentate ligands can coordinate through two different donor atoms. Thiocyanate (SCN⁻) can bind through S or N, making it ambidentate. Hence option (C) is correct.

  6. Question 6 (NEET 2026)

    NEET 2026MediumCrystal field splitting and spin-only magnetic moment
    Among the species given below, the spin-only magnetic moment is highest for (Given: Atomic number of Ti = 22, Mn = 25, Fe = 26 and Co = 27)
    1. Option A: [Mn(CN)6]3−\mathrm{[Mn(CN)_6]^{3-}}
    2. Option B: [Fe(CN)6]3−\mathrm{[Fe(CN)_6]^{3-}}
    3. Option C: [Co(NH3)6]3+\mathrm{[Co(NH_3)_6]^{3+}}
    4. Option D: [Ti(H2O)6]3+\mathrm{[Ti(H_2O)_6]^{3+}}
    Show answer & explanation

    Correct answer: (A) [Mn(CN)6]3−\mathrm{[Mn(CN)_6]^{3-}}

    Explanation

    Spin-only magnetic moment: μ=n(n+2) BM\mu = \sqrt{n(n+2)}\ \mathrm{BM}, where nn is the number of unpaired electrons. (A) Mn3+\mathrm{Mn^{3+}} is 3d43d^4. CN−\mathrm{CN^-} is a strong-field ligand, so it is low spin, t2g4t_{2g}^4: n=2n = 2, μ=8≈2.83 BM\mu = \sqrt{8} \approx 2.83\ \mathrm{BM}. (B) Fe3+\mathrm{Fe^{3+}} is 3d53d^5, low spin with CN−\mathrm{CN^-}, t2g5t_{2g}^5: n=1n = 1, μ≈1.73 BM\mu \approx 1.73\ \mathrm{BM}. (C) Co3+\mathrm{Co^{3+}} is 3d63d^6, low spin with NH3\mathrm{NH_3}, t2g6t_{2g}^6: n=0n = 0, diamagnetic. (D) Ti3+\mathrm{Ti^{3+}} is 3d13d^1: n=1n = 1, μ≈1.73 BM\mu \approx 1.73\ \mathrm{BM}. The highest value is for [Mn(CN)6]3−\mathrm{[Mn(CN)_6]^{3-}}, option (A).

  7. Question 7 (NEET 2026)

    NEET 2026MediumBonding & Crystal Field Theory
    Match List I with List II: Choose the correct answer from the options given below :
    1. Option A: A–III, B–IV, C–I, D–II
    2. Option B: A–III, B–I, C–IV, D–II
    3. Option C: A–IV, B–I, C–III, D–II
    4. Option D: A–I, B–III, C–IV, D–II
    Show answer & explanation

    Correct answer: (B) A–III, B–I, C–IV, D–II

    Explanation

    [PtCl₂(NH₃)₂] → square planar; [Co(NH₃)₆]³⁺ → octahedral; [NiCl₄]²⁻ → tetrahedral; [Fe(CO)₅] → trigonal bipyramidal. Hence option (B) is correct.

  8. Question 8 (NEET 2026)

    NEET 2026EasyIUPAC nomenclature and formulas of complexes
    The formula of tetraammineaquachloridocobalt(III) chloride is
    1. Option A: [Co(NH3)4Cl2]×H2O\mathrm{[Co(NH_3)_4Cl_2] \times H_2O}
    2. Option B: [Co(NH3)4]Cl3×H2O\mathrm{[Co(NH_3)_4]Cl_3 \times H_2O}
    3. Option C: [Co(NH3)4(H2O)Cl]Cl\mathrm{[Co(NH_3)_4(H_2O)Cl]Cl}
    4. Option D: [Co(NH3)4(H2O)Cl]Cl2\mathrm{[Co(NH_3)_4(H_2O)Cl]Cl_2}
    Show answer & explanation

    Correct answer: (D) [Co(NH3)4(H2O)Cl]Cl2\mathrm{[Co(NH_3)_4(H_2O)Cl]Cl_2}

    Explanation

    The name means the coordination sphere has 4 ammine (NH3\mathrm{NH_3}), 1 aqua (H2O\mathrm{H_2O}) and 1 chlorido (Cl−\mathrm{Cl^-}) ligand around Co3+\mathrm{Co^{3+}}, and chloride is the counter ion. Charge on the complex ion =+3+4(0)+0+(−1)=+2= +3 + 4(0) + 0 + (-1) = +2, i.e. [Co(NH3)4(H2O)Cl]2+\mathrm{[Co(NH_3)_4(H_2O)Cl]^{2+}}. Two Cl−\mathrm{Cl^-} ions are needed to balance it, so the formula is [Co(NH3)4(H2O)Cl]Cl2\mathrm{[Co(NH_3)_4(H_2O)Cl]Cl_2}, option (D). Option (C) has the wrong charge balance. Options (A) and (B) do not have water and a single chloride inside the coordination sphere.

  9. Question 9 (NEET 2026)

    NEET 2026EasyGeometrical isomerism: fac and mer isomers
    The complex which has facial and meridional isomers is (Given : py = pyridine and en = H2N−CH2−CH2−NH2\mathrm{H_2N-CH_2-CH_2-NH_2})
    1. Option A: [Cr(py)3(Cl)3]\mathrm{[Cr(py)_3(Cl)_3]}
    2. Option B: [Cr(H2O)6]3+\mathrm{[Cr(H_2O)_6]^{3+}}
    3. Option C: [Co(NH3)4(H2O)2]3+\mathrm{[Co(NH_3)_4(H_2O)_2]^{3+}}
    4. Option D: [Ni(en)2(H2O)2]2+\mathrm{[Ni(en)_2(H_2O)_2]^{2+}}
    Show answer & explanation

    Correct answer: (A) [Cr(py)3(Cl)3]\mathrm{[Cr(py)_3(Cl)_3]}

    Explanation

    Facial (fac) and meridional (mer) isomers occur in octahedral complexes of the type [Ma3b3]\mathrm{[Ma_3b_3]}. In fac, the three identical ligands sit on one face of the octahedron; in mer, they lie around a meridian. (A) [Cr(py)3Cl3]\mathrm{[Cr(py)_3Cl_3]} is Ma3b3\mathrm{Ma_3b_3}, so it shows fac and mer isomers. (B) [Cr(H2O)6]3+\mathrm{[Cr(H_2O)_6]^{3+}} is Ma6\mathrm{Ma_6} and has no geometrical isomers. (C) [Co(NH3)4(H2O)2]3+\mathrm{[Co(NH_3)_4(H_2O)_2]^{3+}} is Ma4b2\mathrm{Ma_4b_2} and shows only cis–trans isomerism. (D) [Ni(en)2(H2O)2]2+\mathrm{[Ni(en)_2(H_2O)_2]^{2+}} is M(AA)2b2\mathrm{M(AA)_2b_2} and shows cis–trans isomerism (the cis form is also optically active), not fac–mer. So the answer is option (A).

  10. Question 10 (NEET 2026)

    NEET 2026EasyIonisation of complexes in solution
    A 1 : 3 electrolyte in an aqueous solution is
    1. Option A: [CoCl2(NH3)4]Cl\mathrm{[CoCl_2(NH_3)_4]Cl}
    2. Option B: [CoCl(NH3)5]Cl2\mathrm{[CoCl(NH_3)_5]Cl_2}
    3. Option C: [Co(NH3)6]Cl3\mathrm{[Co(NH_3)_6]Cl_3}
    4. Option D: [Co(NH3)3(NO2)3]\mathrm{[Co(NH_3)_3(NO_2)_3]}
    Show answer & explanation

    Correct answer: (C) [Co(NH3)6]Cl3\mathrm{[Co(NH_3)_6]Cl_3}

    Explanation

    Only the ions outside the square brackets are released in solution. (A) [CoCl2(NH3)4]Cl→[CoCl2(NH3)4]++Cl−\mathrm{[CoCl_2(NH_3)_4]Cl \rightarrow [CoCl_2(NH_3)_4]^+ + Cl^-}: 1 : 1 electrolyte. (B) [CoCl(NH3)5]Cl2→[CoCl(NH3)5]2++2Cl−\mathrm{[CoCl(NH_3)_5]Cl_2 \rightarrow [CoCl(NH_3)_5]^{2+} + 2Cl^-}: 1 : 2 electrolyte. (C) [Co(NH3)6]Cl3→[Co(NH3)6]3++3Cl−\mathrm{[Co(NH_3)_6]Cl_3 \rightarrow [Co(NH_3)_6]^{3+} + 3Cl^-}: 1 : 3 electrolyte. (D) [Co(NH3)3(NO2)3]\mathrm{[Co(NH_3)_3(NO_2)_3]} is a neutral complex and a non-electrolyte. So the answer is option (C).

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