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Inorganic Chemistry

GATE Chemistry (CY) — Coordination Chemistry previous year questions

36 questions · 2005 · all with verified answer · last checked 2026-11-06

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Q1 · 2005-2021 · 2 marks

In the trigonal bipyramidal crystal field, the d orbital with the highest energy is
  • (a) d_{xy}
  • (b) d_{x^2-y^2}
  • (c) d_{yz}
  • (d) d_{z^2}
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Answer: (d)

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Q2 · 2005-2021 · 2 marks

The pair of ions that most commonly forms complexes with coordination number 2 is
  • (a) Cd (II) and Hg (II)
  • (b) Cu (II) and Hg (I)
  • (c) Cd (II) and Hg (I)
  • (d) Cu (I) and Hg (II)
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Answer: (d)

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Q3 · 2005-2021 · 2 marks

The set of ions expected to show Jahn-Teller distortion in their complexes is
  • (a) Ti(III), Cu(II), High-spin Fe(III)
  • (b) Cu(I), Ni(II), High-spin Fe(III)
  • (c) Cu(II), Low-spin Fe(III), Ti(III)
  • (d) Low-spin-Fe(III), Mn(II), Cu(I)
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Answer: (c)

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Q4 · 2005-2021 · 2 marks

The CORRECT order of the rate of exchange of water molecules between the coordination sphere and the bulk is:
  • (a) \mathrm{Cr^{3+} < Al^{3+} < Ni^{2+}}
  • (b) \mathrm{Cr^{3+} < Al^{3+} < Ni^{2+} < Cr^{2+}}
  • (c) \mathrm{Cr^{3+} < Ni^{2+} < Cr^{2+} < Al^{3+}}
  • (d) \mathrm{Cr^{3+} < Cr^{2+} < Al^{3+} < Ni^{2+}}
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Answer: (b)

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Q5 · 2005-2021 · 2 marks

The crystal structure of \mathrm{Pb}_{3}\mathrm{O}_{4} contains
  • (a) octahedral and tetrahedra units
  • (b) only octahedral units
  • (c) octahedral and pyramidal units
  • (d) octahedral and square-planar units
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Answer: (c)

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Q6 · 2005-2021 · 2 marks

The compound which shows L \leftarrow M charge transfer is
  • (a) \mathrm{Ni(CO)_4}
  • (b) \mathrm{K_2Cr_2O_7}
  • (c) HgO
  • (d) [\mathrm{Ni(H_2O)_6}]^{2+}
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Answer: (a)

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Q7 · 2005-2021 · 2 marks

The expected magnetic moments of the first – row transition metal complexes and those of the lanthanide metal complexes are usually calculated using
  • (a) \mu_{\mathrm{s.o}} equation (s.o. = spin only) for both lanthanide and transition metal complexes
  • (b) \mu_{\mathrm{s.o}} equation for lanthanide metal complexes and \mu_{J} equation for transition metal complexes
  • (c) \mu_{\mathrm{s.o}} equation for transition metal complexes and \mu_{J} equation for lanthanide metal complexes
  • (d) \mu_{L+S} equation for transition metal complexes and \mu_{\mathrm{s.o}} equation for lanthanide metal complexes
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Answer: (c)

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Q8 · 2005-2021 · 2 marks

Designate the following complexes X, Y and Z as inert or labile:
\mathrm{X = [Al(C_2O_4)_3]^{3-}},\ \mathrm{Y = [V(H_2O)_6]^{2+}},\ \mathrm{Z = [Cr(C_2O_4)_3]^{3-}}
  • (a) X and Y are inert; Z is labile
  • (b) X and Z are labile; Y is inert.
  • (c) X is inert; Y and Z are labile
  • (d) X is labile; Y and Z are inert.
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Answer: (d)

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Q9 · 2005-2021 · 2 marks

The number of unpaired electron(s) present in the species [\mathrm{Fe(H_2O)_5(NO)}]^{2+} which is formed during 'brown ring test' is:
  • (a) 2
  • (b) 3
  • (c) 4
  • (d) 5
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Answer: (b)

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Q10 · 2005-2021 · 2 marks

\mathrm{Fe}_{3}\mathrm{O}_{4} and \mathrm{Co}_{3}\mathrm{O}_{4} are metal oxides having spinel structure. Considering their CFSEs, the correct statement regarding their structure is
  • (a) both have normal spinel structure
  • (b) both have inverse spinel structure
  • (c) \mathrm{Fe}_{3}\mathrm{O}_{4} has normal and \mathrm{Co}_{3}\mathrm{O}_{4} has inverse spinel structure
  • (d) \mathrm{Fe}_{3}\mathrm{O}_{4} has inverse and \mathrm{Co}_{3}\mathrm{O}_{4} has normal spinel structure
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Answer: (d)

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Q11 · 2005-2021 · 2 marks

The d–d absorption band of \mathrm{[Fe(H_2O)_6]^{2+}} is split due to
  • (a) presence of octahedral geometry
  • (b) static Jahn–Teller distortion
  • (c) dynamic Jahn–Teller distortion
  • (d) presence of trigonal bipyramidal geometry
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Answer: (c)

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Q12 · 2005-2021 · 2 marks

The crystal-field symbol for the ground-state of \left[\mathrm{Mn}(\mathrm{CN})_{6}\right]^{4-} is
  • (a) {}^{2}\mathrm{T}_{2\mathrm{g}}
  • (b) {}^{1}\mathrm{A}_{1\mathrm{g}}
  • (c) {}^{5}\mathrm{E}_{\mathrm{g}}
  • (d) {}^{6}\mathrm{A}_{1\mathrm{g}}
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Answer: (a)

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Q13 · 2005-2021 · 2 marks

The complex that exists as a pair of enantiomers is
  • (a) trans-[\mathrm{Co(H_2NCH_2CH_2NH_2)_2Cl_2}]^+
  • (b) cis-[\mathrm{Co(NH_3)_4Cl_2}]^+
  • (c) [\mathrm{Pt(PPh_3)(Cl)(Br)(CH_3)}]^-
  • (d) [\mathrm{Co(H_2NCH_2CH_2NH_2)_3}]^{3+}
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Answer: (d)

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Q14 · 2005-2021 · 2 marks

The increasing order of wavelength of absorption for the complex ions (i) [\mathrm{Cr(NH_3)_6}]^{3+} (ii) [\mathrm{CrCl_6}]^{3-} (iii) [\mathrm{Cr(OH_2)_6}]^{3+} (iv) [\mathrm{Cr(CN)_6}]^{3-}, is
  • (a) iv < ii < i < iii
  • (b) iv < iii < ii < i
  • (c) iv < i < iii < ii
  • (d) ii < iii < i < iv
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Answer: (c)

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Q15 · 2005-2021 · 2 marks

The complex with inverse-spinel structure is
  • (a) \mathrm{Co}_{3} \mathrm{O}_{4}
  • (b) \mathrm{Fe}_{3} \mathrm{O}_{4}
  • (c) \mathrm{MgAlO}_{4}
  • (d) \mathrm{Mn}_{3} \mathrm{O}_{4}
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Answer: (b)

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Q16 · 2005-2021 · 2 marks

The geometries of \mathrm{Ni(CO)_4} and \mathrm{[NiCl_4]^{2-}}, respectively, are
  • (a) tetrahedral and square planar
  • (b) square planar and tetrahedral
  • (c) tetrahedral and tetrahedral
  • (d) square planar and square planar
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Answer: (c)

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Q17 · 2005-2021 · 2 marks

The complexes \mathrm{[Co(H_2O)_4Cl_2]NO_2} and \mathrm{[Co(H_2O)_4Cl(NO_2)]Cl} are
  • (a) linkage isomers
  • (b) positional isomers
  • (c) ionization isomers
  • (d) optical isomers
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Answer: (c)

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Q19 · 2005-2021 · 2 marks

Amongst the following, the complex ion that is expected to the highest magnetic moment at room temperature is
  • (a) \left[\mathrm{Ni}(\mathrm{CN})_{4}\right]^{2-}
  • (b) \left[\mathrm{Fe}(\mathrm{CN})_{6}\right]^{3-}
  • (c) \left[\mathrm{Cu}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{2+}
  • (d) \left[\mathrm{Co}(\mathrm{CN})_{6}\right]^{3-}
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Answer: (b)

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Q20 · 2005-2021 · 2 marks

\mathrm{MnCr}_{2}\mathrm{O}_{4} is
  • (a) normal spinel with total CFSE of -15.5\,\mathrm{Dq}
  • (b) inverse spinel with total CFSE of -15.5\,\mathrm{Dq}
  • (c) normal spinel with total CFSE of -24\,\mathrm{Dq}
  • (d) inverse spinel with total CFSE of -24\,\mathrm{Dq}
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Answer: (c)

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Q21 · 2005-2021 · 2 marks

The absorption spectrum of [\mathrm{Ti(H_2O)_6}]^{3+} in solution comprises of a maximum with a shoulder. The reason for the shoulder is
  • (a) ligand-to-metal charge transfer (LMCT)
  • (b) metal-to-ligand charge transfer (MLCT)
  • (c) Jahn-Teller distortion
  • (d) nephelauxetic effect.
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Answer: (c)

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Q22 · 2005-2021 · 2 marks

The intense red color of \left[\mathrm{Fe}(\mathrm{bpy})_{3}\right]^{2+} (bpy =2,2' -bipyridine) is due to)
  • (a) metal-to-ligand charge transfer (MLCT)
  • (b) ligand-to-metal charge transfer (LMCT)
  • (c) d-d transition
  • (d) inter-valence charge transfer (IVCT)
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Answer: (a)

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Q23 · 2005-2021 · 2 marks

The complexes \mathrm{K_2[NiF_6]} and \mathrm{K_3[CoF_6]} are
  • (a) both paramagnetic
  • (b) both diamagnetic
  • (c) paramagnetic and diamagnetic, respectively
  • (d) diamagnetic and paramagnetic, respectively
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Answer: (d)

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Q24 · 2005-2021 · 2 marks

In the first row high-spin transition metal complexes \mathrm{[M(H_2O)_6]Cl_2} with \mathrm{d^5} and \mathrm{d^7} metal ions, the d-d transitions are
  • (a) spin-forbidden for both
  • (b) spin-allowed for both
  • (c) spin-forbidden for \mathrm{d^5} and spin-allowed for \mathrm{d^7}
  • (d) spin-allowed for \mathrm{d^5} and spin-forbidden for \mathrm{d^7}
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Answer: (c)

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Q25 · 2005-2021 · 2 marks

According to Irving-Williams series, the number of d electrons for the first row transition metal (M) ion having the highest overall stability constant (\log \beta) for \mathrm{[M(EDTA)]^{2-}} is ____
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Answer: 9

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Q26 · 2005-2021 · 2 marks

The spinel structure of \mathrm{MgAl_2O_4} has cubic close packed arrangement of oxide ions. The fractions of the octahedral and tetrahedral sites occupied by cations, respectively, are
  • (a) 1/8 and 1/2
  • (b) 1/4 and 1/2
  • (c) 1/2 and 1/4
  • (d) 1/2 and 1/8
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Answer: (d)

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Q27 · 2005-2021 · 2 marks

The water exchange rates for the complex ions follow the order
  • (a) \mathrm{[V(H_2O)_6]^{2+} > [Co(H_2O)_6]^{2+} > [Cr(H_2O)_6]^{3+}}
  • (b) \mathrm{[Cr(H_2O)_6]^{3+} > [Co(H_2O)_6]^{2+} > [V(H_2O)_6]^{2+}}
  • (c) \mathrm{[Co(H_2O)_6]^{2+} > [Cr(H_2O)_6]^{3+} > [V(H_2O)_6]^{2+}}
  • (d) \mathrm{[Co(H_2O)_6]^{2+} > [V(H_2O)_6]^{2+} > [Cr(H_2O)_6]^{3+}}
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Answer: (d)

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Q28 · 2005-2021 · 2 marks

The lowest energy \mathrm{d} \rightarrow \mathrm{d} transition of the complexes follow the order
  • (a) [\mathrm{Cr(H_2O)_6}]^{3+} < [\mathrm{Cr(NH_3)_6}]^{3+} < [\mathrm{Cr(CN)_6}]^{3-}
  • (b) [\mathrm{Cr(CN)_6}]^{3-} < [\mathrm{Cr(NH_3)_6}]^{3+} < [\mathrm{Cr(H_2O)_6}]^{3+}
  • (c) [\mathrm{Cr(CN)_6}]^{3-} < [\mathrm{Cr(H_2O)_6}]^{3+} < [\mathrm{Cr(NH_3)_6}]^{3+}
  • (d) [\mathrm{Cr(NH_3)_6}]^{3+} < [\mathrm{Cr(CN)_6}]^{3-} < [\mathrm{Cr(H_2O)_6}]^{3+}
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Answer: (a)

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Q29 · 2005-2021 · 2 marks

The symmetry label of valence p orbitals of a metal ion in an octahedral ligand field is
  • (a) t_{1g}
  • (b) t_{1u}
  • (c) e_g + a_{1g}
  • (d) t_{2g}
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Answer: (b)

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Q30 · 2005-2021 · 2 marks

Spectroscopic ground state term symbols of cobalt ions in \mathrm{[Co(H_2O)_6]^{2+}} and \mathrm{[CoCl_4]^{2-}} respectively are
  • (a) {}^{2}T_{1g} and {}^{4}A_{2}
  • (b) {}^{4}T_{1g} and {}^{4}A_{2}
  • (c) {}^{4}T_{2g} and {}^{4}T_{1}
  • (d) {}^{2}T_{1} and {}^{4}A_{1}
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Answer: (b)

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Q31 · 2005-2021 · 2 marks

For an inverse spinel, \mathrm{AB_2O_4}, the A and B, respectively, can be
  • (a) Ni(II) and Ga(III)
  • (b) Zn(II) and Fe(III)
  • (c) Fe(II) and Cr(III)
  • (d) Mn(II) and Mn(III)
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Answer: (a)

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Q32 · 2005-2021 · 2 marks

The reaction of \mathrm{NiBr}_{2} with two equivalents of \mathrm{PPh}_{3} in \mathrm{CS}_{2} at -78^{\circ} \mathrm{C} gives a red-colored diamagnetic complex. \left[\mathrm{NiBr}_{2}\left(\mathrm{PPh}_{3}\right)_{2}\right]. This transforms to a green-colored paramagnetic complex with the same molecular formula at 25^{\circ} \mathrm{C}. The geometry and the number of unpaired electrons in the green-colored complex, respectively, are:
  • (a) square planar and 2
  • (b) tetrahedral and 2
  • (c) square planar and 4
  • (d) tetrahedral and 1
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Answer: (b)

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Q33 · 2005-2021 · 2 marks

The rate of the substitution reaction of \left[\mathrm{Co}(\mathrm{CN})_{5} \mathrm{Cl}\right]^{3-} with \mathrm{OH}^{-}to give \left[\mathrm{Co}(\mathrm{CN})_{5}(\mathrm{OH})\right]^{3-}
  • (a) is inversely proportional to the concentration of \mathrm{OH}^{-} perchlorate ion, +7 , charge transfer
  • (b) depends on the concentrations of both \left[\mathrm{Co}(\mathrm{CN})_{5} \mathrm{Cl}\right]^{3-} and \mathrm{OH}^{-} chromium chloride, +3 , d-d transition
  • (c) depends on the concentration of \left[\mathrm{Co}(\mathrm{CN})_{5} \mathrm{Cl}\right]^{3-} only dichromate ion, +6 and +6 , charge transfer
  • (d) is directly proportional to the concentration of \mathrm{OH}^{-}only HCl . The red-orange complex, the oxidation state of its central element(s), and the origin of its color, respec tively, are: chromic acid, +6 , charge transfer
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Answer: (c)

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Q34 · 2005-2021 · 2 marks

The \Delta_{0} of \left[\mathrm{Cr}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{3+},\left[\mathrm{CrF}_{6}\right]^{3-} and \left[\mathrm{Cr}(\mathrm{CN})_{6}{ }^{3-}\right. follows the order:
  • (a) \left[\mathrm{CrF}_{6}\right]^{3-}>\left[\mathrm{Cr}(\mathrm{CN})_{6}\right]^{3-}>\left[\mathrm{Cr}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{3+}
  • (b) \left[\mathrm{Cr}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{3+}>\left[\mathrm{CrF}_{6}\right]^{3-}>\left[\mathrm{Cr}(\mathrm{CN})_{6}\right]^{3-}
  • (c) \left[\mathrm{CrF}_{6}\right]^{3-}>\left[\mathrm{Cr}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{3+}>\left[\mathrm{Cr}(\mathrm{CN})_{6}\right]^{3-}
  • (d) \left[\mathrm{Cr}(\mathrm{CN})_{6}\right]^{3-}>\left[\mathrm{Cr}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{3+}>\left[\mathrm{CrF}_{6}\right]^{3-}
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Answer: (d)

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Q35 · 2005-2021 · 2 marks

The spin-only magnetic moment of \left[\mathrm{Co}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{2+} (rounded off to one decimal place) is ____ BM.
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Answer: 3.9

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Q36 · 2005-2021 · 2 marks

The correct order of increasing intensity (molar absorptivity) of the UV-visible absorption bands for the ions \left[\mathrm{Ti}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{3+},\left[\mathrm{Mn}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{2+},\left[\mathrm{CrO}_{4}\right]^{2-}, and \left[\mathrm{NiCl}_{4}\right]^{2-} is
  • (a) \left[\mathrm{Ti}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{3+}<\left[\mathrm{NiCl}_{4}\right]^{2-}<\left[\mathrm{CrO}_{4}\right]^{2-}<\left[\mathrm{Mn}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{2+}
  • (b) \left[\mathrm{Ti}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{3+}<\left[\mathrm{Mn}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{2+}<\left[\mathrm{CrO}_{4}\right]^{2-}<\left[\mathrm{NiCl}_{4}\right]^{2-}
  • (c) \left[\mathrm{Mn}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{2+}<\left[\mathrm{Ti}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{3+}<\left[\mathrm{NiCl}_{4}\right]^{2-}<\left[\mathrm{CrO}_{4}\right]^{2-}
  • (d) \left[\mathrm{NiCl}_{4}\right]^{2-}<\left[\mathrm{Ti}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{3+}<\left[\mathrm{Mn}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{2+}<\left[\mathrm{CrO}_{4}\right]^{2-} COORDINATION ANSWERS KEY
    1.(a)2.(d)3.(a)4.(d)5.(b)6.(b)7.(d)
    8.(c)9.(c)10.(a)11.(b)12.(c)13.(b)14.(a)
    15.(c)16.(d)17.(d)18.(a)19.(d)20(b)21.(d)
    22.(c)23.(b)24.(c)25.(?)26.(b)27.(?)28.(d)
    29.(b)30.(d)31.(a)32.(c)33.(a)34.(?)35.(?)
    36.(d)37.(d)38.(b)39.(c)40.(c)41.(b)42.(b)
    43.(d)44.(c)45.(c)46.(c)47.(c)48.(9)49.(a)
    50.(b)51.(c)52.(c)53.(a)54.(d)55.(d)56.(c)
    57.(c)58.(9)59.(2.0)60.(d)61.(b)62.(c)63.(c)
    64.(d)65.(d)66.(a)67.(b)68.(b)69.(a)70.(?)
    71.(?)72.(?)73.(?)74.(?)75.(2)76.(a)77.(b)
    78.(c)79.(?)80.(d)81.(3.9)82.(c)
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Answer: (c)

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