Coordination Compounds JEE Advanced previous year questions with solutions

5 solved JEE Advanced questions on Coordination Compounds, free to read — no sign-in needed. The full chapter has 53 questions; sign in to attempt the remaining 48 in the exam simulator.

  1. Q1JEE Advanced Adv 2026 (Paper 2)
    Consider that the coordinating atoms of the ligands in ciscis-[Co(NH3_3)4_4Cl2_2]Cl and mermer-[Co(NH3_3)3_3Cl3_3] octahedral complexes are at the vertices of an octahedron. The sum of total number of the triangular faces in both the complexes having one N atom and two Cl atoms at their corners is ____.
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    Answer: 6

    In an octahedral complex, the six coordinating atoms are located at the vertices of an octahedron, which has 8 triangular faces. Each face is formed by 3 vertices, and any two adjacent (cis) vertices form an edge that is shared by exactly two faces. For the ciscis-[Co(NH3_3)4_4Cl2_2]+^+ complex: The two Cl atoms are at adjacent (cis) positions, forming exactly one Cl-Cl edge. This edge is shared by two triangular faces. Since the remaining four vertices are occupied by N atoms, the third vertex of each of these two faces must be an N atom. Therefore, there are 2 faces with exactly two Cl atoms and one N atom. For the mermer-[Co(NH3_3)3_3Cl3_3] complex: The three Cl atoms are in a meridional arrangement, meaning two Cl atoms are trans to each other and the third is cis to both. This arrangement forms exactly two Cl-Cl edges. Since the three Cl atoms do not occupy the vertices of the same face (unlike the facfac isomer), no face contains three Cl atoms. Each of the two Cl-Cl edges is shared by two faces, yielding 2×2=42 \times 2 = 4 distinct faces that contain exactly two Cl atoms. The third vertex in all these 4 faces is an N atom. Therefore, there are 4 faces with exactly two Cl atoms and one N atom. The sum of the total number of such faces in both complexes is 2+4=62 + 4 = 6. Answer: 66
  2. Q2JEE Advanced Adv 2026 (Paper 1)
    The total number of all possible isomers for the square planar complex with formula K[M(NCS)(NO2)(gly)]\text{K}[\text{M(NCS)(NO}_2\text{)(gly)}] is ____. (MM = metal ion and gly = NH2CH2COO\text{NH}_2\text{CH}_2\text{COO}^-)
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    Answer: 8

    The given complex is K[M(NCS)(NO2)(gly)]\text{K}[\text{M(NCS)(NO}_2\text{)(gly)}]. The complex anion is [M(NCS)(NO2)(gly)][\text{M(NCS)(NO}_2\text{)(gly)}]^{-}. The ligands present in the complex are: 1. gly\text{gly}^- (glycinate): An unsymmetrical bidentate ligand coordinating through nitrogen (N) and oxygen (O). Let this be represented as (AB)(AB). 2. NCS\text{NCS}^-: An ambidentate monodentate ligand that can coordinate through nitrogen (-NCS\text{-NCS}) or sulfur (-SCN\text{-SCN}). 3. NO2\text{NO}_2^-: An ambidentate monodentate ligand that can coordinate through nitrogen (-NO2\text{-NO}_2) or oxygen (-ONO\text{-ONO}). First, we find the number of linkage isomers due to the ambidentate ligands: NCS\text{NCS}^- has 2 linkage modes (N or S). NO2\text{NO}_2^- has 2 linkage modes (N or O). Number of linkage combinations = 2×2=42 \times 2 = 4. For each linkage combination, the complex is of the type [M(a)(b)(AB)][\text{M}(a)(b)(AB)], where aa and bb are monodentate ligands and ABAB is an unsymmetrical bidentate ligand. In a square planar geometry, the bidentate ligand (AB)(AB) must occupy adjacent (cis) positions. The monodentate ligands aa and bb will occupy the remaining two positions. This gives rise to 2 geometrical isomers for each linkage combination: 1. Ligand aa is trans to A (and bb is trans to B). 2. Ligand aa is trans to B (and bb is trans to A). Since square planar complexes of this type possess a molecular plane of symmetry, they do not exhibit optical isomerism. Total number of isomers = (Number of linkage combinations) ×\times (Number of geometrical isomers per combination) Total isomers = 4×2=84 \times 2 = 8. Answer: 88
  3. Q3JEE Advanced Adv 2026 (Paper 1)
    Reaction of PtF6\text{PtF}_6 with oxygen (O2\text{O}_2) gas results in the formation of an ionic compound, X+Y\textbf{X}^+\textbf{Y}^-. Correct statement(s) is(are)
    1. A.The bond order of X+\textbf{X}^+ is 1.51.5.
    2. B.Valence dd-orbitals of the metal ion in X+Y\textbf{X}^+\textbf{Y}^- has 55 electrons.
    3. C.PtF6\text{PtF}_6 acts as an oxidant in this reaction.
    4. D.PtF6\text{PtF}_6 acts as a fluorinating agent in this reaction.
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    Answer: B,C

    The reaction between O2\text{O}_2 and PtF6\text{PtF}_6 is: O2+PtF6O2+[PtF6]\text{O}_2 + \text{PtF}_6 \rightarrow \text{O}_2^+[\text{PtF}_6]^- Here, X+X^+ is O2+\text{O}_2^+ and YY^- is [PtF6][\text{PtF}_6]^-. For O2+\text{O}_2^+, the total number of electrons is 1515. The molecular orbital configuration is σ1s2σ1s2σ2s2σ2s2σ2pz2π2px2π2py2π2px1\sigma_{1s}^2 \sigma_{1s}^{*2} \sigma_{2s}^2 \sigma_{2s}^{*2} \sigma_{2p_z}^2 \pi_{2p_x}^2 \pi_{2p_y}^2 \pi_{2p_x}^{*1}. The bond order is 1052=2.5\dfrac{10 - 5}{2} = 2.5. Thus, the bond order is not 1.51.5. In the complex ion [PtF6][\text{PtF}_6]^-, the oxidation state of Pt\text{Pt} is +5+5. The ground state electronic configuration of Pt\text{Pt} is [Xe]4f145d96s1[\text{Xe}] 4f^{14} 5d^9 6s^1. The configuration of Pt5+\text{Pt}^{5+} is [Xe]4f145d5[\text{Xe}] 4f^{14} 5d^5. Therefore, the valence dd-orbitals of the metal ion contain 55 electrons. During the reaction, O2\text{O}_2 loses an electron to form O2+\text{O}_2^+ and PtF6\text{PtF}_6 gains an electron to form [PtF6][\text{PtF}_6]^-. Since PtF6\text{PtF}_6 accepts an electron, it undergoes reduction and acts as an oxidant. Since no fluorine atoms are transferred to O2\text{O}_2, PtF6\text{PtF}_6 does not act as a fluorinating agent. Answer: Valence dd-orbitals of the metal ion in X+Y\textbf{X}^+\textbf{Y}^- has 55 electrons.; PtF6\text{PtF}_6 acts as an oxidant in this reaction.
  4. Q4JEE Advanced Adv 2025 (Paper 1)
    The correct order of the wavelength maxima of the absorption band in the ultraviolet-visible region for the given complexes is
    1. A.[Co(CN)6]3<[Co(NH3)6]3+<[Co(NH3)5(H2O)]3+<[Co(NH3)5(Cl)]2+\left[\mathrm{Co}(\mathrm{CN})_6\right]^{3-} \lt \left[\mathrm{Co}\left(\mathrm{NH}_3\right)_6\right]^{3+} \lt \left[\mathrm{Co}\left(\mathrm{NH}_3\right)_5\left(\mathrm{H}_2 \mathrm{O}\right)\right]^{3+} \lt \left[\mathrm{Co}\left(\mathrm{NH}_3\right)_5(\mathrm{Cl})\right]^{2+}
    2. B.[Co(NH3)5(Cl)]2+<[Co(NH3)5(H2O)]3+<[Co(NH3)6]3+<[Co(CN)6]3\left[\mathrm{Co}\left(\mathrm{NH}_3\right)_5(\mathrm{Cl})\right]^{2+} \lt \left[\mathrm{Co}\left(\mathrm{NH}_3\right)_5\left(\mathrm{H}_2 \mathrm{O}\right)\right]^{3+} \lt \left[\mathrm{Co}\left(\mathrm{NH}_3\right)_6\right]^{3+} \lt \left[\mathrm{Co}(\mathrm{CN})_6\right]^{3-}
    3. C.[Co(CN)6]3<[Co(NH3)5(Cl)]2+<[Co(NH3)5(H2O)]3+<[Co(NH3)6]3+\left[\mathrm{Co}(\mathrm{CN})_6\right]^{3-} \lt \left[\mathrm{Co}\left(\mathrm{NH}_3\right)_5(\mathrm{Cl})\right]^{2+} \lt \left[\mathrm{Co}\left(\mathrm{NH}_3\right)_5\left(\mathrm{H}_2 \mathrm{O}\right)\right]^{3+} \lt \left[\mathrm{Co}\left(\mathrm{NH}_3\right)_6\right]^{3+}
    4. D.[Co(NH3)6]3+<[Co(CN)6]3<[Co(NH3)5(Cl)]2+<[Co(NH3)5(H2O)]3+\left[\mathrm{Co}\left(\mathrm{NH}_3\right)_6\right]^{3+} \lt \left[\mathrm{Co}(\mathrm{CN})_6\right]^{3-} \lt \left[\mathrm{Co}\left(\mathrm{NH}_3\right)_5(\mathrm{Cl})\right]^{2+} \lt \left[\mathrm{Co}\left(\mathrm{NH}_3\right)_5\left(\mathrm{H}_2 \mathrm{O}\right)\right]^{3+}
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    Answer: (A)

    ΔO1λ\Delta_{\mathrm{O}} \propto \frac{1}{\lambda}  The absorb wave length order is [Co(CN)6]3<[Co(NH3)6]3+<[Co(NH3)5H2O]3+<[Co(NH3)5Cl]2+\begin{aligned} &\therefore \text { The absorb wave length order is }\\ &\left[\mathrm{Co}(\mathrm{CN})_6\right]^{3-} \lt \left[\mathrm{Co}\left(\mathrm{NH}_3\right)_6\right]^{3+} \lt \left[\mathrm{Co}\left(\mathrm{NH}_3\right)_5 \mathrm{H}_2 \mathrm{O}\right]^{3+} \lt \left[\mathrm{Co}\left(\mathrm{NH}_3\right)_5 \mathrm{Cl}\right]^{2+} \end{aligned}
  5. Q5JEE Advanced Adv 2024 (Paper 2)
    Among [Co(CN)4]4,[Co(CO)3(NO)],XeF4,[PCl4]+,[PdCl4]2,[ICl4],[Cu(CN)4]3\left[\mathrm{Co}(\mathrm{CN})_4\right]^{4-},\left[\mathrm{Co}(\mathrm{CO})_3(\mathrm{NO})\right], \mathrm{XeF}_4,\left[\mathrm{PCl}_4\right]^{+},\left[\mathrm{PdCl}_4\right]^{2-},\left[\mathrm{ICl}_4\right]^{-},\left[\mathrm{Cu}(\mathrm{CN})_4\right]^{3-} and P4\mathrm{P}_4 the total number of species with tetrahedral geometry is _______
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    Answer: 5

    [Co(CN)4]4,[Co(CO)3NO],[PCl4]+,[Cu(CN)4]3 & P4\left[\mathrm{Co}(\mathrm{CN})_4\right]^{4-},\left[\mathrm{Co}(\mathrm{CO})_3 \mathrm{NO}\right],\left[\mathrm{PCl}_4\right]^{+},\left[\mathrm{Cu}(\mathrm{CN})_4\right]^{3-} ~\&~ \mathrm{P}_4 are with tetrahedral geometry.

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Coordination Compounds in JEE Advanced: previous year question analysis

Coordination Compounds has appeared 53 times in JEE Advanced between 2006 and 2026, making it the 7th most-asked of 93 chapters and about 2.2% of the bank. Over the last 5 years it has averaged 2.4 questions per year.

Total PYQs
53
Years covered
2006–2026
Weightage rank
#7 of 93
Share of bank
2.2%

How many Coordination Compounds questions appeared each year

Coordination Compounds JEE Advanced question count by year
YearQuestionsRelative volume
20153
20163
20171
20183
20191
20201
20213
20221
20232
20244
20252
20263

Question formats used in Coordination Compounds

  • Single-correct MCQ28
  • Numerical / integer answer16
  • Multiple-correct MCQ9

How Coordination Compounds compares with nearby chapters

Counts are computed from AcadXL’s own JEE Advanced question bank, tagged chapter- and sub-topic-wise and checked against official answer keys. Sign in to attempt the 53 Coordination Compounds questions with solutions.