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Inorganic Chemistry

CSIR NET Chemical Science — Organometallic Compounds previous year questions

112 questions · 2011–2021 · all with verified answer · last checked 2026-11-06

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Q1 · June 2021 · 2 marks

Consider following statement(s) in the context of NO and CO ligands
  • (a) In the bent mode, NO donates three electrons to the metal center. A only
  • (b) In IR spectrum, the v_{\mathrm{NO}} for the bent nitrosyl ligand typically lies between 1525 and 1690 \mathrm{~cm}^{-1} B and C
  • (c) The HOMO of NO and CO are \pi^{*} and \sigma orbitals, respectively A and C
  • (d) A and B
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Answer: (b)

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Q2 · June 2021 · 2 marks

The correct geometries for the metal carbonyl clusters, A-C
  • (a) \left[\mathrm{Ru}_{6}(\mathrm{CO})_{17} \mathrm{~B}\right]^{-} A: pentagonal bipyramidal, B: trigonal prismatic, and C:tetrahedral
  • (b) \left[\mathrm{Os}_{6}(\mathrm{CO})_{18} \mathrm{P}\right]^{-} A: pentagonal bipyramidal, B: octahedral, and C: square
  • (c) \left[\mathrm{Os}_{4}(\mathrm{CO})_{16}\right] are A: octahedral, B: trigonal prismatic, and C: tetrahedral
  • (d) A: octahedral, B: trigonal prismatic, and C: square
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Answer: (d)

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Q3 · 2020 · 2 marks

Among the following complexes, the one showing the highest rate of substitution of a CO ligand on heating with one equivalent of \mathrm{PPh_3} in decalin, is
  • (a) (\eta^5\text{-}\mathrm{C_5H_5})\mathrm{Mn(CO)_3}
  • (b) (\eta^5\text{-}\mathrm{C_5Ph_5})\mathrm{Mn(CO)_3}
  • (c) (\eta^5\text{-}\mathrm{C_5Me_5})\mathrm{Mn(CO)_3}
  • (d) (\eta^5\text{-indenyl})\mathrm{Mn(CO)_3}
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Answer: (d)

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Q4 · 2020 · 2 marks

The geometry/shape of the Fe4 core of the cluster \left[\mathrm{Fe}{ }_{4} \mathrm{C}(\mathrm{CO})_{12}\right]^{-2} is
  • (a) tetrahedron
  • (b) square pyramid
  • (c) butterfly
  • (d) trigonal bipyramid
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Answer: (c)

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Q5 · 2020 · 2 marks

The number of peaks with relative intensities observed in the { }^{1} \mathrm{H} \mathrm{NMR} spectra of [ \left(\mathbf{C p})_{2} \mathbf{F e}(\mathbf{C O})_{2}\right] at +30^{\circ} \mathrm{C} and -80^{\circ} \mathrm{C} in diethyl ether are, respectively
  • (a) Two peaks (1:1) and four peaks (5:2:2:1)
  • (b) One peak and two peaks (1:1)
  • (c) Two peaks (1:1) at both the temperatures
  • (d) One peak and four peaks (5: 2: 2: 1)
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Answer: (a)

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Q6 · 2019 · 2 marks

The rate-determining step in the catalytic synthesis of acetic acid by Monsanto process is
  • (a) oxidative addition of \mathrm{CH_3I} to \mathrm{[RhI_2(CO)_2]^-}
  • (b) migration of \mathrm{CH_3} group to CO of \mathrm{[RhI_3(CO)_2(CH_3)]^-}
  • (c) loss of \mathrm{CH_3COI} from \mathrm{[RhI_3(CO)_2(COCH_3)]^-}
  • (d) coordination of CO to \mathrm{[RhI_3CO(COCH_3)]^-}
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Answer: (a)

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Q7 · June 2019 · 2 marks

The number of \mathrm{Ni}-\mathrm{Ni} bonds in \left[\mathrm{CpNi}\left(\mu-\mathrm{PPh}_{2}\right)\right]_{2} complex obeying the 18 electron rule is
  • (a) 0
  • (b) 1
  • (c) 2
  • (d) 3
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Answer: (a)

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Q8 · 2018 · 2 marks

For the reaction of trans- [\operatorname{Ir} \mathrm{X}(\mathrm{CO})(\mathrm{PPh} 3) 2](\mathrm{X}=\mathrm{F}, \mathrm{Cl}, \mathrm{Br}, \mathrm{I}) with O 2 , correct order of variation of rate with X is
  • (a) \mathrm{Br}>\mathrm{I}>\mathrm{F}>\mathrm{Cl}
  • (b) \mathrm{F}>\mathrm{Cl}>\mathrm{Br}>\mathrm{I}
  • (c) \mathrm{F} \approx \mathrm{Cl} \approx \mathrm{Br} \approx 1
  • (d) I > Br > Cl > F
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Answer: (d)

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Q9 · June 2019 · 2 marks

The organic species isolobal to \left[\mathrm{Fe}(\mathrm{CO})_{2}\left(\mathrm{PPh}_{3}\right)\right]^{-}is
  • (a) \mathrm{CH}_{2}{ }^{+}
  • (b) \mathrm{CH}^{-}
  • (c) \mathrm{CH}_{3}
  • (d) CH
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Answer: (d)

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Q10 · 2018 · 2 marks

The correct statements about \left[\mathrm{Ru}_{6} \mathrm{C}(\mathrm{CO})_{17}\right] cluster from the following (1) it is an 86 electron cluster (2) it is a closo structure type (3) its shape is capped square pyramid (4) carbon interacts with all the Ru centres in the cluster are
  • (a) 1, 2, 3 and 4
  • (b) 1 and 2 only
  • (c) 1, 2 and 3
  • (d) 1, 2 and 4
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Answer: (d)

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Q11 · 2018 · 2 marks

Considering \sigma-bonding only, in the MO diagram of a metal complex with trigonal bipyramidal (TBP) geometry, the d-orbitals which remain non-bonding are
  • (a) \mathrm{dz}^{2} and \mathrm{d}_{\mathrm{xz}}
  • (b) \mathrm{d}_{\mathrm{xz}} and \mathrm{d}_{\mathrm{yz}}
  • (c) \mathrm{d}_{\mathrm{x}^{2}-\mathrm{v}^{2}} and \mathrm{d}_{\mathrm{xy}}
  • (d) \mathrm{dz}^{2} and \mathrm{d}_{\mathrm{yz}}
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Answer: (b)

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Q12 · Dec 2019 · 2 marks

The most stable vanadium species in aqueous medium is
  • (a) \left[\mathrm{V}\left(\mathrm{H}_{2} \mathrm{O}\right)_{5}(\mathrm{OH})\right]^{+2}
  • (b) \left[\mathrm{VO}\left(\mathrm{H}_{2} \mathrm{O}\right)_{5}\right]^{+2}
  • (c) \left[\mathrm{VO}\left(\mathrm{H}_{2} \mathrm{O}\right)_{5}\right]^{+}
  • (d) \left[\mathrm{V}\left(\mathrm{H}_{2} \mathrm{O}\right)_{4}(\mathrm{OH})_{2}\right]^{+2}
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Answer: (b)

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Q13 · Dec 2019 · 2 marks

The correct order of metal-carbon distance is
  • (a) \mathrm{Fe}\left(\eta^{5}-\mathrm{Cp}\right)_{2}>\mathrm{Co}\left(\eta^{5}-\mathrm{Cp}\right)_{2}>\mathrm{Ni}\left(\eta^{5}-\mathrm{Cp}\right)_{2}
  • (b) \mathrm{Fe}\left(\eta^{5}-\mathrm{Cp}\right)_{2}>\mathrm{Ni}\left(\eta^{5}-\mathrm{Cp}\right)_{2}>\mathrm{Co}\left(\eta^{5}-\mathrm{Cp}\right)_{2}
  • (c) \mathrm{Ni}\left(\eta^{5}-\mathrm{Cp}\right)_{2}>\mathrm{Fe}\left(\eta^{5}-\mathrm{Cp}\right)_{2}>\mathrm{Co}\left(\eta^{5}-\mathrm{Cp}\right)_{2}
  • (d) \mathrm{Ni}\left(\eta^{5}-\mathrm{Cp}\right)_{2}>\mathrm{Co}\left(\eta^{5}-\mathrm{Cp}\right)_{2}>\mathrm{Fe}\left(\eta^{5}-\mathrm{Cp}\right)_{2}
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Answer: (d)

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Q14 · Dec 2019 · 2 marks

The rate-determining step in the catalytic synthesis of acetic acid by Monsanto process is
  • (a) oxidative addition of \mathrm{CH}_{3} \mathrm{I} to \left[\mathrm{RhI}_{2}(\mathrm{CO})_{2}\right]^{-}
  • (b) migration of \mathrm{CH}_{3} group to CO of \left[\mathrm{RhI}_{3}(\mathrm{CO})_{2}\left(\mathrm{CH}_{3}\right)\right]^{-}
  • (c) loss of \mathrm{CH}_{3} \mathrm{COI} from \left[\mathrm{RhI}_{3}(\mathrm{CO})_{2}\left(\mathrm{COCH}_{3}\right)\right]^{-}
  • (d) coordination of CO to \left[\mathrm{RhI}_{3} \mathrm{CO}\left(\mathrm{COCH}_{3}\right)\right]^{-}
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Answer: (a)

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Q15 · Dec 2019 · 2 marks

The cluster types of \left[\mathrm{Fe}_{5}(\mathrm{CO})_{14} \mathrm{~N}\right]^{-}and \left[\mathrm{Co}_{6}(\mathrm{CO})_{13} \mathrm{~N}\right]^{-}are, respectively,
  • (a) nido-, nido
  • (b) nido-, closo
  • (c) closo-, nido
  • (d) closo-, closo
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Answer: (b)

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Q16 · Dec 2019 · 2 marks

Among the following complexes, the one showing the highest rate of substitution of a CO ligand on heating with one equivalent of PPh3 in decalin, is
  • (a) \left(\eta^{5}-\mathrm{C}_{5} \mathrm{H}_{5}\right) \mathrm{Mn}(\mathrm{CO})_{3}
  • (b) \left(\eta^{5}-\mathrm{C}_{5} \mathrm{Ph}_{5}\right) \mathrm{Mn}(\mathrm{CO})_{3}
  • (c) \left(\eta^{5}-\mathrm{C}_{5} \mathrm{Me}_{5}\right) \mathrm{Mn}(\mathrm{CO})_{3}
  • (d) ( \eta^{5}-indenyl) \mathrm{Mn}(\mathrm{CO})_{3}
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Answer: (d)

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Q17 · 2018 · 2 marks

The correct order of acceptor ability of the phosphorus ligands is
  • (a) \mathrm{PMe_3 > PPh_3 > P(OPh)_3 > PF_3}
  • (b) \mathrm{PF_3 > P(OPh)_3 > PPh_3 > PMe_3}
  • (c) \mathrm{PF_3 > PMe_3 > PPh_3 > P(OPh)_3}
  • (d) \mathrm{P(OPh)_3 > PF_3 > PMe_3 > PPh_3}
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Answer: (b)

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Q18 · 2018 · 2 marks

The number of Ni-Ni bonds in [\mathrm{CpNi}(\mu\text{-}\mathrm{PPh_2})]_2 complex obeying the 18 electron rule is
  • (a) 0
  • (b) 1
  • (c) 2
  • (d) 3
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Answer: (a)

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Q19 · 2018 · 2 marks

The organic species isolobal to \mathrm{[Fe(CO)_2(PPh_3)]^-} is
  • (a) \mathrm{CH_2^+}
  • (b) \mathrm{CH^-}
  • (c) \mathrm{CH_3}
  • (d) CH
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Answer: (d)

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Q20 · June 2018 · 2 marks

The correct of \mathrm{C}-\mathrm{O} bond length is
  • (a) \mathrm{H}_{3} \mathrm{~B} . \mathrm{CO}>\left[\mathrm{Mn}(\mathrm{CO})_{6}\right]^{+}>\left[\mathrm{Cr}(\mathrm{CO})_{6}\right]>\left[\mathrm{V}(\mathrm{CO})_{6}\right]^{-}
  • (b) \left[\mathrm{V}(\mathrm{CO})_{6}\right]^{-}>\left[\mathrm{Cr}(\mathrm{CO})_{6}\right]>\left[\mathrm{Mn}(\mathrm{CO})_{6}\right]^{+}>\mathrm{H}_{3} \mathrm{~B} . \mathrm{CO}
  • (c) \left[\mathrm{Mn}(\mathrm{CO})_{6}\right]^{+}>\mathrm{H}_{3} \mathrm{~B} . \mathrm{CO}>\left[\mathrm{V}(\mathrm{CO})_{6}\right]^{-}<\left[\mathrm{Cr}(\mathrm{CO})_{6}\right]
  • (d) \left[\mathrm{Cr}(\mathrm{CO})_{6}\right]>\left[\mathrm{V}(\mathrm{CO})_{6}\right]^{-}>\mathrm{H}_{3} \mathrm{~B} . \mathrm{CO}>\left[\mathrm{Mn}(\mathrm{CO})_{6}\right]^{+}
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Answer: (b)

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Q21 · 2018 · 2 marks

Which of the following are NOT closo clusters?
\left[\left\{\mathrm{Co}\left(\eta^{5}-\mathrm{C}_{5} \mathrm{H}_{5}\right)\right\} 2\left(\mathrm{C}_{2} \mathrm{~B}_{6} \mathrm{H}_{8}\right)\right](\mathrm{A})\left[\mathrm{B}_{4} \mathrm{C}_{2} \mathrm{H}_{8}\right](\mathrm{B})\left[\mathrm{B}_{10} \mathrm{H}_{13}\left\{\left(\mathrm{Au}\left(\mathrm{PPh}_{3}\right)\right\}\right](\mathrm{C})\left[\mathrm{C}_{2} \mathrm{~B}_{8} \mathrm{H}_{10}\right](\mathrm{D})\right.
  • (a) (C) and (D)
  • (b) (A) and (B)
  • (c) (A) and (C)
  • (d) (B) and (C)
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Answer: (d)

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Q22 · 2018 · 2 marks

The structures of \left[\mathrm{Re}_{2} \mathrm{C}_{18}\right]^{-2}(\mathrm{~A}) and \left[\mathrm{Os}_{2} \mathrm{Cl}_{8}\right]^{-2}(\mathrm{~B}) are made up of two \mathrm{MCl}_{4} units. For these structure which statement is correct?
  • (a) (A) and (B) both have \mathrm{MCl}_{4} units eclipsed.
  • (b) (A) and (B) both have \mathrm{MCl}_{4} units staggered.
  • (c) (A) has both \mathrm{MCl}_{4} units staggered and (B) has both \mathrm{MCl}_{4} units eclipsed.
  • (d) (A) has both \mathrm{MCl}_{4} units eclipsed and (B) has both \mathrm{MCl}_{4} units staggered.
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Answer: (d)

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Q23 · Dec 2018 · 2 marks

The correct order of acceptor ability of the phosphorus ligands is
  • (a) \mathrm{PMe}_{3}>\mathrm{PPh}_{3}>\mathrm{P}(\mathrm{OPh})_{3}>\mathrm{PF}_{3}
  • (b) \mathrm{PF}_{3}>\mathrm{P}(\mathrm{OPh})_{3}>\mathrm{PPh}_{3}>\mathrm{PMe}_{3}
  • (c) \mathrm{PF}_{3}>\mathrm{PMe}_{3}>\mathrm{PPh}_{3}>\mathrm{P}(\mathrm{OPh})_{3}
  • (d) \mathrm{P}(\mathrm{OPh})_{3}>\mathrm{PF}_{3}>\mathrm{PMe}_{3}>\mathrm{PPh}_{3}
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Answer: (b)

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Q24 · 2018 · 2 marks

Identify the correct statement(s) for \mathrm{H}_{3} \mathrm{~B} . \mathrm{CO}
  • (a) \mathbf{s p}^{\mathbf{2}} hybridized orbital of \mathbf{B} accepts the lone pair of \mathbf{C O}.
  • (b) Its \overline{\mathbf{v}}_{\mathrm{CO}} value is more than that for free CO
  • (c) Formal oxidation state of C is +4 in the compound
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Answer: (b)

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Q25 · 2018 · 2 marks

The VCN in \left[\mathrm{Fe}(\mathrm{CN})_{6}\right]^{-3}(\mathrm{~A}) and \left[\mathrm{Fe}(\mathrm{CN})_{6}\right]^{-4}(\mathrm{~B}) and \mathrm{V}_{\mathrm{co}} in \left[\mathrm{Cr}(\mathrm{CO})_{3}\left(\mathrm{NH}_{3}\right)_{3}\right](\mathrm{C}) and \left[\mathrm{Cr}(\mathrm{CO})_{6}\right](\mathrm{D}) are compared below. The pair with correct order is
  • (a) A > B ; C > D
  • (b) A > B ; C < D
  • (c) A < B ; C > D
  • (d) A < B ; C < D
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Answer: (b)

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Q26 · 2018 · 2 marks

The cluster type and geometry of the species \left[\mathrm{R} \mathrm{h}_{9} \mathrm{P}(\mathrm{CO})_{21}\right]^{-2} are
  • (a) closo, tricapped trigonal prism
  • (b) arachno, trigonal prism
  • (c) nido, capped square antiprism
  • (d) nido, bicapped trigonal prism
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Answer: (c)

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Q27 · 2017 · 2 marks

Choose the isoelectronic pair among the following: A. \mathrm{[V(CO)_6]} B. [\mathrm{Cu}(\eta^5\text{-}\mathrm{C_5H_5})(\mathrm{CO})] C. \mathrm{[Co(CO)_4]^-} D. \mathrm{[IrCl(CO)(PPh_3)]}
  • (a) A and B
  • (b) B and C
  • (c) C and D
  • (d) A and D
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Answer: (b)

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Q28 · June 2017 · 2 marks

Choose the isoelectronic pair among the following:
  • (a) \left[\mathrm{V}(\mathrm{CO})_{6}\right] A and B
  • (b) \left[\mathrm{Cu}\left(\eta^{5}-\mathrm{C}_{5} \mathrm{H}_{5}\right)(\mathrm{CO})\right] B and C
  • (c) \left[\mathrm{Co}(\mathrm{CO})_{4}\right]^{-} C and D
  • (d) \left[\operatorname{IrCl}(\mathrm{CO})\left(\mathrm{PPh}_{3}\right)\right] A and D
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Answer: (b)

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Q29 · 2017 · 2 marks

An organometallic fragment that is isolobal to \mathrm{CH}_{3}{ }^{+}is
  • (a) \left[\mathrm{Fe}(\mathrm{CO})_{5}\right]
  • (b) \left[\mathrm{Mn}(\mathrm{CO})_{5}\right]
  • (c) \left[\mathrm{Cr}(\mathrm{CO})_{5}\right]
  • (d) \left[\mathrm{Ni}(\mathrm{CO})_{3}\right]^{+}
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Answer: (c)

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Q30 · 2017 · 2 marks

The number of bonding molecular orbitals and the number of available skeletal electrons in \left[\mathrm{B}_{6} \mathrm{H}_{6}\right]^{-2}, respectively, are:
  • (a) 7 and 14
  • (b) 6 and 12
  • (c) 18 and 12
  • (d) 11 and 14
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Answer: (a)

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Q31 · June 2017 · 2 marks

Addition of \mathrm{NaBH}_{4} to \left[\left(\eta^{5}-\mathrm{C}_{\mathrm{p}}\right) \mathrm{Fe}\left(\eta^{6}-\mathrm{C}_{6} \mathrm{H}_{6}\right)\right]^{+}will give
  • (a) \left[\left(\eta^{5}-\mathrm{Cp}\right) \mathrm{Fe}(\mathrm{H})_{2}\right]
  • (b) \left[\left(\eta^{5}-\mathrm{Cp}\right) \mathrm{Fe}(\mathrm{H})\left(\eta^{6}-\mathrm{C}_{6} \mathrm{H}_{6}\right)\right]
  • (c) \left[\left(\eta^{5}-\mathrm{Cp}\right) \mathrm{Fe}\left(\eta^{6}-\mathrm{C}_{6} \mathrm{H}_{6}\right)\right]
  • (d) \left[\left(\eta^{5}-\mathrm{Cp}\right) \mathrm{Fe}\left(\eta^{6}-\mathrm{C}_{6} \mathrm{H}_{7}\right)\right]
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Answer: (d)

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Q32 · 2017 · 2 marks

Among the following species isolobal to \mathbf{C H}_{\mathbf{2}} are
  • (a) \mathrm{CpCr}(\mathrm{CO})_{2} A, C and E
  • (b) CpCu B, C and D
  • (c) \mathrm{Ni}(\mathrm{CO})_{2} B, C and E
  • (d) \mathrm{Cr}(\mathrm{CO})_{4} E. \mathrm{Fe}(\mathrm{CO})_{4} A, B and D
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Answer: (c)

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Q33 · 2017 · 2 marks

According to Wade's rules, the cluster type and geometry of \left[\mathrm{Sn}_{9}\right]^{-4}, respectively, are
  • (a) closo and tricapped trigonal prismatic
  • (b) nido and monocapped square-antiprismatic
  • (c) arachno and heptagonal bipyramidal
  • (d) closo and monocapped square antiprismatic
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Answer: (b)

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Q34 · 2016 · 2 marks

\mathrm{CpM}\left[\mathrm{Cp}\right. is \left.\left(\eta^{5}-\mathrm{C}_{5} \mathrm{H}_{5}\right)\right] fragment isolobal with a BH fragment is
  • (a) CpGe
  • (b) CpMn
  • (c) CpRu
  • (d) CpCo
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Answer: (d)

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Q35 · 2016 · 2 marks

The number of metal-metal bonds in \left[\mathrm{Co}_{2} \mathrm{Fe}_{2}(\mathrm{CO})_{11}\left(\eta_{4}-\mathrm{PPh}\right)_{2}\right] is
  • (a) 3
  • (b) 4
  • (c) 5
  • (d) 6
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Answer: (b)

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Q36 · 2016 · 2 marks

Choose the correct option for carbonyl fluoride with respect to bond angle and bond length
  • (a) \angle \mathrm{F}-\mathrm{C}-\mathrm{F}>\angle \mathrm{F}-\mathrm{C}-\mathrm{O} and \mathrm{C}-\mathrm{F}>\mathrm{C}-\mathrm{O}
  • (b) \angle \mathrm{F}-\mathrm{C}-\mathrm{F}>\angle \mathrm{F}-\mathrm{C}-\mathrm{O} and \mathrm{C}-\mathrm{F}<\mathrm{C}-\mathrm{O}
  • (c) \angle \mathrm{F}-\mathrm{C}-\mathrm{F}<\angle \mathrm{F}-\mathrm{C}-\mathrm{O} and \mathrm{C}-\mathrm{F}>\mathrm{C}-\mathrm{O}
  • (d) \angle \mathrm{F}-\mathrm{C}-\mathrm{F}<\angle \mathrm{F}-\mathrm{C}-\mathrm{O} and \mathrm{C}-\mathrm{F}<\mathrm{C}-\mathrm{O}
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Answer: (c)

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Q37 · 2016 · 2 marks

The { }^{1} \mathrm{H} NMR spectrum of \left[\mathrm{Ru}\left(\eta^{4}-\mathrm{C}_{8} \mathrm{H}_{8}\right)(\mathrm{CO})_{3}\right] at 23^{\circ} \mathrm{C} consists of a sharp single line. The number of signals observed at low temperature (-140 °C) in its spectrum is
  • (a) 8
  • (b) 6
  • (c) 4
  • (d) 2
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Answer: (c)

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Q38 · 2016 · 2 marks

The numbers of skeletal electrons present in the compounds \mathrm{C}_{2} \mathrm{~B}_{3} \mathrm{H}_{5}, \mathrm{C}_{2} \mathrm{~B}_{4} \mathrm{H}_{6}, and \mathrm{B}_{5} \mathrm{H}_{9} are, respectively
  • (a) 10, 12 and 12
  • (b) 12, 14 and 14
  • (c) 10, 12 and 14
  • (d) 12, 14 and 12
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Answer: (b)

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Q39 · 2016 · 2 marks

The rate of alkene coordination to \left[\mathrm{PtCl}_{4}\right]^{-2} is highest for
  • (a) norbornene
  • (b) ethylene
  • (c) cyclohexene
  • (d) 1-butene
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Answer: (a)

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Q40 · 2016 · 2 marks

Consider the following statements, I and II: \mathrm{I}:\left[\mathrm{Rh}(\mathrm{CO})_{2} \mathrm{I}_{2}\right]^{-}catalytically converts \mathrm{CH}_{3} \mathrm{I} and CO to \mathrm{CH}_{3} \mathrm{COI} II : \left[\mathrm{Rh}(\mathrm{CO})_{2} \mathrm{I}_{2}\right]^{-}is diamagnetic in nature The correct from the following is
  • (a) I and II are correct and II is an explanation of I
  • (b) I and II are correct and II is not an explanation of I
  • (c) I is correct and II is incorrect
  • (d) I and II are incorrect
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Answer: (b)

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Q41 · 2016 · 2 marks

According to Wade's rules, the correct structural types of \left[\mathrm{Co}\left(\eta^{5}-\mathrm{C}_{5} \mathrm{H}_{5}\right) \mathrm{B}_{4} \mathrm{H}_{8}\right] and \left[\mathrm{Mn}\left(\eta^{2}-\mathrm{B}_{3} \mathrm{H}_{8}\right)(\mathrm{CO})_{4}\right] are
  • (a) closo and nido
  • (b) nido and arachno
  • (c) closo and arachno
  • (d) nido and nido
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Answer: (b)

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Q42 · 2016 · 2 marks

The correct geometry of \left[\mathrm{Rh}_{6} \mathrm{C}(\mathrm{CO})_{15}\right]^{-2} is
  • (a) octahedron
  • (b) pentagonal pyramid
  • (c) trigonal prism
  • (d) monocapped square pyramid
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Answer: (c)

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Q43 · 2015 · 2 marks

According to Wade's theory the anion \mathrm{[B_{12}H_{12}]^{2-}} adopts
  • (a) closo-structure
  • (b) arachno-structure
  • (c) hypo-structure
  • (d) nido-structure
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Answer: (a)

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Q44 · 2015 · 2 marks

The reaction of \mathrm{SbCl_3}, with 3 equivalents of EtMgBr yields compound X. Two equivalents of \mathrm{SbI_3} react with one equivalent of X to give Y. In the solid state, Y has a 1D-polymeric structure in which each Sb is in a square pyramidal environment. Compounds X and Y respectively, are
  • (a) \mathrm{SbEt_3}, and [\mathrm{Sb(Et)I_2}]_n
  • (c) \mathrm{SbEt_3}, and [\mathrm{SbEt_2Br_2}]_n
  • (b) \mathrm{Sb(Et_2)Cl} and [\mathrm{Sb(Et)Cl}]_n
  • (d) \mathrm{Sb(Et)Br_2} and [\mathrm{SbEt(I)(Br)}]_n
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Answer: (a)

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Q45 · 2015 · 2 marks

Amongst the following (A) [\mathrm{Mn}(\eta^5\text{-Cp})(\mathrm{CO})_3] (B) [\mathrm{Os}(\eta^5\text{-Cp})_2] (C) [\mathrm{Ru}(\eta^5\text{-Cp})_2] and (D) [\mathrm{Fe}(\eta^5\text{-Cp})_2] the compounds with most shielded and deshielded Cp protons respectively, are
  • (a) D and A
  • (b) D and B
  • (c) C and A
  • (d) C and B
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Answer: (a)

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Q46 · 2015 · 2 marks

The approximate positions of \nu_{\mathrm{co}} bands (\mathrm{cm^{-1}}) in the solid-state infrared spectrum and the Fe-Fe bond order in \mathrm{[Fe(\eta^5\text{-}C_5H_5)(\mu\text{-}CO)(CO)]_2} (non-centrosymmetric) respectively, are
  • (a) (2020, 1980, 1800) and one
  • (b) (2020, 1980, 1800) and two
  • (c) (2020, 1980) and one
  • (d) (2143) and one
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Answer: (a)

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Q47 · 2015 · 2 marks

The binding modes of NO in 18 electron compounds [\mathrm{Co}(\mathrm{CO}) 3(\mathrm{NO})] and [\mathrm{Ni}(\eta 5-\mathrm{Cp})(\mathrm{NO})], respectively, are
  • (a) linear and bent
  • (b) bent and linear
  • (c) linear and linear
  • (d) bent and bent
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Answer: (c)

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Q48 · 2015 · 2 marks

The role of copper salt as co-catalyst in Wacker process is
  • (a) oxidation of \operatorname{Pd}(0) by Cu (II)
  • (b) oxidation of \operatorname{Pd}(\mathbf{0}) by \mathbf{C u}(\mathbf{I})
  • (c) oxidation of Pd(II) by Cu(I)
  • (d) oxidation of Pd(II) by Cu(II)
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Answer: (a)

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Q49 · June 2015 · 2 marks

According to Wade's theory the anion \left[\mathrm{B}_{12} \mathrm{H}_{12}\right]^{2-} adopts
  • (a) closo-structure
  • (b) arachno-structure
  • (c) hypo-structure
  • (d) nido-structure
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Answer: (a)

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Q50 · June 2015 · 2 marks

The reaction of \mathrm{SbCl}_{3}, with 3 equivalents of EtMgBr yields compound X . Two equivalents of \mathrm{SbI}_{3} react with one equivalent of X to give Y . In the solid state, Y has a 1 D -polymeric structure in which each Sb is in a square pyramidal environment. Compounds X and Y respectively, are
  • (a) \mathrm{SbEt}_{3}, and \left[\mathrm{Sb}(\mathrm{Et}) \mathrm{I}_{2}\right]_{\mathrm{n}}
  • (c) \mathrm{SbEt}_{3}, and \left[\mathrm{SbEt}_{2} \mathrm{Br}_{2}\right]_{\mathrm{n}}
  • (b) \mathrm{Sb}\left(\mathrm{Et}_{2}\right) \mathrm{Cl} and [\mathrm{Sb}(\mathrm{Et}) \mathrm{Cl}]_{\mathrm{n}}
  • (d) \mathrm{Sb}(\mathrm{Et}) \mathrm{Br}_{2} and [\mathrm{SbEt}(\mathrm{I})(\mathrm{Br})]_{\mathrm{n}}
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Answer: (a)

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Q51 · 2015 · 2 marks

The following statements are given regarding the agostic interaction C-H----Ir observed in \left[\operatorname{Ir}\left(\mathrm{Ph}_{3} \mathrm{P}\right)_{3} \mathrm{Cl}\right].
  • (a) Upfield shift of C-H proton in 1H NMR spectrum
  • (b) Increased acid character of C-H
  • (c) \bar{v} co- in IR spectrum shifts to higher wavenumber
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Answer: (c)

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Q52 · June 2015 · 2 marks

Amongst the following
  • (a) \left[\mathrm{Mn}\left(\eta^{5}-\mathrm{Cp}\right)(\mathrm{CO})_{3}\right] D and A
  • (b) \left[\mathrm{Os}\left(\eta^{5}-\mathrm{Cp}\right)_{2}\right] D and B
  • (c) \left[\mathrm{Ru}\left(\eta^{5}-\mathrm{Cp}\right)_{2}\right] and C and A
  • (d) \left[\mathrm{Fe}\left(\eta^{5}-\mathrm{Cp}\right)_{2}\right] the compounds with most shielded and deshielded \mathrm{C}_{\mathrm{p}} protons respectively, are C and B
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Answer: (a)

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Q53 · 2015 · 2 marks

Total number of vertices in metal clusters \left[\mathrm{Ru}_{6}(\mathrm{C})(\mathrm{CO})_{17}\right]\left[\mathrm{Os}_{5}(\mathrm{C})(\mathrm{CO})_{15}\right] and \left[\mathbf{R u}_{\mathbf{5}}(\mathbf{C})(\mathbf{C O})_{\mathbf{1 6}}\right] are 6, 5 and 5, respectively. The predicted structures of these complexes, respectively are
  • (a) closo, nido and nido
  • (b) closo, nido and arachno
  • (c) arachno, closo and nido
  • (d) arachno, nido and closo
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Answer: (b)

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Q54 · 2015 · 2 marks

The W-W bond order in \left[\mathrm{W}\left(\eta^{5}-\mathrm{C}_{5} \mathrm{H}_{5}\right)(\mu-\mathrm{Cl})(\mathrm{CO})_{2}\right]_{2} is
  • (a) three
  • (b) two
  • (c) one
  • (d) zero
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Answer: (d)

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Q55 · 2015 · 2 marks

For the reaction of \left[\mathrm{Fe}\left(\eta^{5}-\mathrm{C}_{5} \mathrm{H}_{5}\right)\left(\mathrm{CH}_{3}\right)(\mathrm{CO})_{2}\right] with \mathrm{PMe}_{3}, the main intermediate is
  • (a) \left[\mathrm{Fe}\left(\eta^{5}-\mathrm{C}_{5} \mathrm{H}_{5}\right)\left(\mathrm{CH}_{3}\right)(\mathrm{CO})_{2}\left(\mathrm{PMe}_{3}\right)\right]
  • (b) \left[\mathrm{Fe}\left(\eta^{5}-\mathrm{C}_{5} \mathrm{H}_{5}\right)\left(\mathrm{COCH}_{3}\right)(\mathrm{CO})\right]
  • (c) \left[\mathrm{Fe}\left(\eta^{3}-\mathrm{C}_{5} \mathrm{H}_{5}\right)(\mathrm{CH} 3)(\mathrm{CO})_{2}\right]
  • (d) ) \left[\mathrm{Fe}\left(\eta^{3}-\mathrm{C}_{5} \mathrm{H}_{5}\right)\left(\mathrm{COCH}_{3}\right)(\mathrm{CO})\left(\mathrm{PMe}_{3}\right)\right]
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Answer: (b)

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Q56 · 2015 · 2 marks

For uranocene, the correct statement(s) is/are
  • (a) oxidation state of uranium is '+4'
  • (b) it has cyclooctatetraenide ligands
  • (c) it is bent sandwich compound
  • (d) it has '-2' charge.
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Answer: (a)

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Q57 · Dec 2015 · 2 marks

The final products of the reaction of carbonyl metalates \left[\mathrm{V}(\mathrm{CO})_{6}\right]^{-}and \left[\mathrm{Co}(\mathrm{CO})_{4}\right]- with \mathrm{H}_{3} \mathrm{PO}_{4} respectively, are
  • (a) \mathrm{V}(\mathrm{CO})_{6} and \mathrm{HCo}(\mathrm{CO})_{4}
  • (b) \mathrm{HV}(\mathrm{CO})_{6} and \mathrm{Co}_{2}(\mathrm{CO})_{8}
  • (c) \left[\mathrm{H}_{2} \mathrm{~V}(\mathrm{CO})_{6}\right]^{+}and \mathrm{HCo}(\mathrm{CO})_{4}
  • (d) \mathrm{V}(\mathrm{CO})_{6} and \mathrm{Co}_{2}(\mathrm{CO})_{8}
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Answer: (a)

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Q58 · 2015 · 2 marks

The number of valence electrons provided by \left[\mathrm{Ru}(\mathrm{CO})_{3}\right] fragment towards cluster bonding is
  • (a) 1
  • (b) 14
  • (c) 6
  • (d) 2
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Answer: (d)

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Q59 · Dec 2015 · 2 marks

Heating a sample of \left[\left(\eta^{5}-\mathrm{C}_{5} \mathrm{H}_{5}\right) \mathrm{Mo}(\mathrm{CO})_{3}\right]_{2} results in the formation of \left[\left(\eta^{5}-\mathrm{C}_{5} \mathrm{H}_{5}\right) \mathrm{Mo}(\mathrm{CO})_{2}\right] with elimination of 2 equivalents of CO. The Mo-Mo bond order in this reaction changes from
  • (a) 2 to 3
  • (b) 1 to 2
  • (c) 1 to 3
  • (d) 2 to 4
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Answer: (c)

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Q60 · 2014 · 2 marks

Amongst the following which is not isolobal pairs
  • (a) \mathrm{Mn(CO)_5}, \mathrm{CH_3}
  • (b) \mathrm{Fe(CO)_4}, O
  • (c) \mathrm{Co(CO)_3}, \mathrm{R_2Si}
  • (d) \mathrm{Mn(CO)_5}, RS
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Answer: (c)

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Q61 · 2014 · 2 marks

Complexes \mathrm{HM(CO)_5} and \mathrm{[((\eta^5\text{-}C_5H_5)M'(CO)_3]_2} obey the 18-electron rule. Identify M and M' and their {}^{1}\mathrm{H} NMR chemical shifts relative to TMS.
  • (a) M = Mn, -7.5; M' = Cr, 4.10
  • (b) M = Cr, -4.10; M' = Mn, -7.5
  • (c) M = V, -7.5; M' = Cr, 4.10
  • (d) M = Mn, -10.22; M' = Fe, 2.80
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Answer: (a)

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Q62 · 2014 · 2 marks

The ligand(s) that is (are) fluxional in [(\eta^{5}-\mathrm{C}_{5}\mathrm{H}_{5})(\eta-\mathrm{C}_{5}\mathrm{H}_{5})\mathrm{Fe}(\mathrm{CO})_{2}] in the temperature range 221-298\mathrm{K}, is (are)
  • (a) \eta^{5}-\mathrm{C}_{5}\mathrm{H}_{5}
  • (b) \eta^{1}-\mathrm{C}_{5}\mathrm{H}_{5}
  • (c) \eta^{5}-\mathrm{C}_{5}\mathrm{H}_{5} and \mathrm{CO}
  • (d) \eta^{1}-\mathrm{C}_{5}\mathrm{H}_{5} and \mathrm{CO}
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Answer: (b)

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Q63 · 2014 · 2 marks

The typical electronic configurations of the transition metal centre for oxidative addition
  • (a) \mathrm{d}^{0} and \mathrm{d}^{8}
  • (b) \mathrm{d}^{6} and \mathrm{d}^{8}
  • (c) \mathrm{d}^{8} and \mathrm{d}^{10}
  • (d) \mathrm{d}^{5} and \mathrm{d}^{10}
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Answer: (c)

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Q64 · 2014 · 2 marks

The oxidation state of Ni and the number of metal-metal bonds in \left[\mathrm{Ni}_{2}(\mathrm{CO})_{6}\right]^{2-} that are consistent with the 18 electron rule are Ni (-II), I bond (b) Ni(IV), 2 bonds (c) Ni(-I), 1 bond (d) Ni(IV), 3 bonds
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Answer: (c)

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Q65 · 2014 · 2 marks

{ }^{1} \mathrm{H} NMR spectrum of \left.\left[\eta^{5}-\mathrm{C}_{5} \mathrm{H}_{5} \mathrm{Rh}\right)\left(\mathrm{C}_{2} \mathrm{H}_{4}\right)_{2}\right] at -20^{\circ} \mathrm{C} shows a typical \mathrm{AA}^{\prime} \mathrm{XX}^{\prime} pattern in the olefinic region. On increasing the temperature to -70^{\circ} \mathrm{C}, the separate lines collapse into a single line which is due to
  • (a) free rotation of the ethylene ligand about the metal-olefin bond
  • (b) interamolecular exchange between the ethylene ligands
  • (c) intermolecular exchange between the ethylene ligands
  • (d) change in hapticity of the cyclopentadienyl ligand
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Answer: (a)

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Q66 · June 2014 · 2 marks

Amongst the following which is not isolobal pairs
  • (a) \mathrm{Mn}(\mathrm{CO})_{5}, \mathrm{CH}_{3}
  • (b) \mathrm{Fe}(\mathrm{CO})_{4}, O
  • (c) \mathrm{Co}(\mathrm{CO})_{3}, \mathrm{R}_{2} \mathrm{Si}
  • (d) \mathrm{Mn}(\mathrm{CO})_{5}, RS
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Answer: (c)

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Q67 · 2014 · 2 marks

The hepticities 'x' and 'y' of the arene moieties in the diamagnetic complex \left[\left(\eta^{\mathrm{x}}-\mathrm{C}_{6} \mathrm{H}_{6}\right) \mathrm{Ru}\left(\eta^{\mathrm{y}}-\mathrm{C}_{6} \mathrm{H}_{6}\right)\right] respectively are
  • (a) 6 and 6
  • (b) 4 and 4
  • (c) 4 and 6
  • (d) 6 and 2
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Answer: (c)

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Q68 · 2014 · 2 marks

The rate of the reaction \mathrm{Ni}(\mathrm{CO})_{4}+\mathrm{PPh}_{3} \xrightarrow{\Delta}\left[\mathrm{Ni}(\mathrm{CO})_{3}\left(\mathrm{PPh}_{3}\right)\right]+\mathrm{CO} depends on
  • (a) Concentration of both the reactants Butanoic acid
  • (b) Concentration of \mathrm{Ni}(\mathrm{CO})_{4} only Butanal
  • (c) Concentration of \mathrm{PPh}_{3} only 2-butanone
  • (d) The steric bulk of \mathrm{PPh}_{3} 8 Methylpropanoate
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Answer: (b)

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Q69 · Dec 2014 · 2 marks

The product of the reaction of propene, \mathrm{CO} and \mathrm{H}_{2} in the presence of \mathrm{Co}_{2}(\mathrm{CO})_{8} as a catalyst is
  • (a) Butanoic acid
  • (b) Butanal
  • (c) 2-butanone
  • (d) Methylpropanoate
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Answer: (b)

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Q70 · 2014 · 2 marks

Reductive elimination step in hydrogenation of alkenes by Wilkinson catalyst results in (neglecting solvent in coordination sphere of Rh)
  • (a) T-shaped \left[\mathrm{Rh}\left(\mathrm{PPh}_{3}\right)_{2} \mathrm{Cl}\right]
  • (b) Trigonal-planar \left[\mathrm{Rh}\left(\mathrm{PPh}_{3}\right)_{2} \mathrm{Cl}\right]^{2+}
  • (c) T-shaped \left[\mathrm{Rh}(\mathrm{H})\left(\mathrm{PPh}_{3}\right) \mathrm{Cl}\right]^{+}
  • (d) Trigonal-planar \left[\mathrm{Rh}(\mathrm{H})\left(\mathrm{PPh}_{3}\right)_{2}\right]
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Answer: (a)

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Q71 · 2014 · 2 marks

\mathrm{NaI}\left(\eta^{5}-\mathrm{C}_{5} \mathrm{H}_{5}\right) \mathrm{Fe}(\mathrm{CO})_{2} ] reacts with \mathrm{Br}_{2} to give A. Reaction of A with \mathrm{LiAlH}_{4} results in B. The proton NMR spectrum of B consists of two singlets of relative intensity 5: 1. Compounds A and B respectively, are
  • (a) \left(\eta^{5}-\mathrm{C}_{5} \mathrm{H}_{5}\right) \mathrm{Fe}(\mathrm{CO})_{2} \mathrm{Br}, and \left(\eta^{5}-\mathrm{C}_{5} \mathrm{H}_{5}\right) \mathrm{Fe}(\mathrm{CO})_{2} \mathrm{H}
  • (b) \left(\eta^{4}-\mathrm{C}_{5} \mathrm{H}_{5}\right) \mathrm{Fe}(\mathrm{CO}){ }_{2} \mathrm{Br}_{2} and \left(\eta^{4}-\mathrm{C}_{5} \mathrm{H}_{5}\right) \mathrm{Fe}(\mathrm{CO})_{2} \mathrm{HBr}
  • (c) \left(\eta^{5}-\mathrm{C}_{5} \mathrm{H}_{5}\right) \mathrm{Fe}(\mathrm{CO})_{2} \mathrm{Br} and \left(\eta^{4}-\mathrm{C}_{5} \mathrm{H}_{5}\right) \mathrm{Fe}(\mathrm{CO})_{2}(\mathrm{H})_{2}
  • (d) \left(\eta^{5}-\mathrm{C}_{5} \mathrm{H}_{5}\right) \mathrm{Fe}(\mathrm{CO})_{2} \mathrm{Br} and \left(\eta^{5}-\mathrm{C}_{5} \mathrm{H}_{5}\right) \mathrm{Fe}(\mathrm{CO})_{2} \mathrm{HBr}
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Answer: (a)

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Q72 · 2014 · 2 marks

The compound that undergoes oxidative addition reaction in presence of \mathrm{H}_{2}, is
  • (a) \left[\mathrm{Mn}(\mathrm{CO})_{5}\right]^{-1}
  • (b) \left[\left(\eta^{5}-\mathrm{C}_{5} \mathrm{H}_{5}\right) \mathrm{MCO}_{3}\right]^{-1}
  • (c) \left[\operatorname{IrCl}(\mathrm{CO})\left(\mathrm{PPh}_{3}\right)_{2}\right]
  • (d) \left[\left(\eta^{5}-\mathrm{C}_{5} \mathrm{H}_{5}\right)_{2} \mathrm{ReH}\right]
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Answer: (c)

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Q73 · 2014 · 2 marks

{ }^{1} \mathrm{H} NMR spectrum of free benzene shows a peak at -7.2 ppm . The expected chemical shift (in ppm) of
  • (c) _{6} \mathrm{H}_{6} ligand in { }^{1} \mathrm{H} \mathrm{NMR} spectrum of \left[\left(\eta^{6}-\mathrm{C}_{6} \mathrm{H}_{6}\right) \mathrm{Cr}(\mathrm{CO})_{3}\right] and the reason for it, if an, is/are 7.2
  • (a) 4.5; disruption of ring current
  • (b) 9.0 ; inductive effect
  • (d) 2.5 combination of inductive effect and disruption of ring current.
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Answer: (a)

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Q74 · Dec 2014 · 2 marks

Complexes \mathrm{HM}(\mathrm{CO})_{5} and \left[\left(\left(\eta^{5}-\mathrm{C}_{5} \mathrm{H}_{5}\right) \mathrm{M}^{\prime}(\mathrm{CO})_{3}\right]_{2}\right. obey the 18 -electron rule. Identify M and \mathrm{M}^{\prime} and their { }^{1} H NMR chemical shifts relative to TMS.
  • (a) \mathrm{M}=\mathrm{Mn},-7.5 ; \mathrm{M}^{\prime}=\mathrm{Cr}, 4.10
  • (b) \mathrm{M}=\mathrm{Cr},-4.10 ; \mathrm{M}^{\prime}=\mathrm{Mn},-7.5
  • (c) \mathrm{M}=\mathrm{V},-7.5 ; \mathrm{M}^{\prime}=\mathrm{Cr}, 4.10
  • (d) \mathrm{M}=\mathrm{Mn},-10.22 \mathrm{M}^{\prime}=\mathrm{Fe}, 2.80
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Answer: (a)

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Q75 · 2013 · 2 marks

The ligand in uranocene is:
  • (a) \mathrm{C_8H_8^{2-}}
  • (b) \mathrm{C_5H_5^{2-}}
  • (c) \mathrm{C_6H_6}
  • (d) \mathrm{C_4H_4^{2-}}
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Answer: (a)

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Q76 · 2013 · 2 marks

The number of metal-metal bonds in \mathrm{Ir_4(CO)_{12}} is
  • (a) 4
  • (b) 6
  • (c) 10
  • (d) 12
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Answer: (b)

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Q77 · 2013 · 2 marks

In a cluster, \mathrm{H_3CoRu_3(CO)_{12}} total number of electrons considered to be involved in its formation is
  • (a) 57
  • (b) 60
  • (c) 63
  • (d) 72
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Answer: (b)

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Q78 · 2013 · 2 marks

The correct statement regarding terminal/bridging CO groups in solid \mathrm{Co_4(CO)_{12}} and \mathrm{Ir_4(CO)_{12}} is
  • (a) both have equal number of bridging CO groups
  • (b) number of bridging CO groups in \mathrm{Co_4(CO)_{12}} is 4
  • (c) the number of terminal CO groups in \mathrm{Co_4(CO)_{12}} is 8
  • (d) the number of bridging CO groups in \mathrm{Ir_4(CO)_{12}} is zero.
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Answer: (d)

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Q79 · 2013 · 2 marks

The oxidation state of molybdenum in \left[\left(\eta^{7} \text {-tropylium }\right) \mathrm{Mo}(\mathrm{CO})_{3}\right]^{+}is:
  • (a) +2
  • (b) +1
  • (c) 0
  • (d) -1
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Answer: (c)

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Q80 · 2013 · 2 marks

The reaction, \left[(\mathrm{CO})_{5} \mathrm{Mn}(\mathrm{Me})\right]+\mathrm{CO} \rightarrow\left[(\mathrm{CO})_{5} \mathrm{Mn}\{\mathrm{C}(\mathrm{O}) \mathrm{Me}\}\right] is an example for
  • (a) oxidative addition
  • (b) electrophilic substitution
  • (c) nucleophilic substitution
  • (d) migratory insertion
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Answer: (d)

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Q81 · June 2013 · 2 marks

The orders of reactivity of ligands, NMe3 PMe3, and CO with complexes MeTiCl, and (\mathrm{CO})_{5} \mathrm{Mo} (thf) are
  • (a) \mathrm{CO}>\mathrm{PMe}_{3}>\mathrm{NMe}_{3} and \mathrm{CO}>\mathrm{NMe}_{3}>\mathrm{PMe}_{3}
  • (b) \mathrm{PMe}_{3}>\mathrm{CO}>\mathrm{NMe}_{3} and \mathrm{NMe}_{3}>\mathrm{CO}>\mathrm{PMe}_{3}
  • (c) \mathrm{NMe}_{3}>\mathrm{PMe}_{3}>\mathrm{CO} and \mathrm{CO}>\mathrm{PMe}_{3}>\mathrm{NMe}_{3}
  • (d) \mathrm{NMe}_{3}>\mathrm{CO}>\mathrm{PMe}_{3} and \mathrm{PMe}_{3}>\mathrm{NMe}_{3}>\mathrm{CO}
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Answer: (c)

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Q82 · 2013 · 2 marks

The number of metal-metal bonds in \left[\mathrm{W} 2(\mathrm{OPh})_{6}\right] is:
  • (a) 1
  • (b) 2
  • (c) 3
  • (d) 4
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Answer: (c)

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Q83 · June 2013 · 2 marks

The number of metal-metal bonds in \operatorname{Ir}_{4}(\mathrm{CO})_{12} is
  • (a) 4
  • (b) 6
  • (c) 10
  • (d) 12
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Answer: (b)

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Q84 · 2013 · 2 marks

The bond order of the metal-metal bond in the dimeric complex \left[\mathrm{Re}_{2} \mathrm{Cl}_{4}\left(\mathrm{PMe}_{2} \mathrm{Ph}\right)_{4}\right] is
  • (a) 4.0
  • (b) 3.5
  • (c) 3.0
  • (d) 2.5
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Answer: (b)

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Q85 · 2013 · 2 marks

Which of the following in NOT suitable as catalyst for hydroformylation?
  • (a) \mathrm{HCo}(\mathrm{CO})_{4}
  • (b) \mathrm{HCo}(\mathrm{CO})_{3} \mathrm{PBu}_{3}
  • (c) \mathrm{HRh}(\mathrm{CO})\left(\mathrm{PPh}_{3}\right)_{3}
  • (d) \mathrm{H}_{2} \mathrm{Rh}\left(\mathrm{PPh}_{3}\right)_{2} \mathrm{Cl}
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Answer: (d)

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Q86 · Dec 2013 · 2 marks

In a cluster, \mathrm{H}_{3} \mathrm{CoRu}_{3}(\mathrm{CO}) 12 total number of electrons considered to be involved in its formation is
  • (a) 57
  • (b) 60
  • (c) 63
  • (d) 72
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Answer: (b)

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Q87 · 2013 · 2 marks

Among the following clusters,
\mathrm{A}=\left[(\mathrm{H}) \mathrm{Co}_{6}(\mathrm{CO})_{15}\right] \mathrm{B}=\left[(\mathrm{H})_{2} \mathrm{Os}_{6}(\mathrm{CO})_{18}\right] \mathrm{C}=\left[(\mathrm{H})_{2} \mathrm{Os}_{5}(\mathrm{CO})_{16}\right]
H is encapsulated in
  • (a) A only
  • (b) B only
  • (c) B and C only
  • (d) A and B only
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Answer: (a)

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Q88 · Dec 2013 · 2 marks

The electrophile \mathrm{Ph}_{3} \mathrm{C} reacts with \left[\left(\eta^{5}-\mathrm{C}_{5} \mathrm{H}_{5}\right) \mathrm{Fe}(\mathrm{CO})_{2}\left(\mathrm{CDMe}_{2}\right)\right]^{+}to give a product A . The product A is formed because
  • (a) Fe is oxidized
  • (b) alkyl is substituted with \mathrm{Ph}_{3} \mathrm{C}
  • (c) Fe-Ph bond is formed
  • (d) Alkyl is converted to alkene
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Answer: (d)

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Q89 · 2013 · 2 marks

On reducing \mathbf{F e}_{3}(\mathbf{C O})_{12} with an excess of sodium, a carbonylate ion is formed. The iron is isoelectronic with
  • (a) \left[\mathrm{Mn}(\mathrm{CO})_{5}\right]^{-}
  • (b) \left[\mathrm{Ni}(\mathrm{CO})_{4}\right]
  • (c) \left[\mathrm{Mn}(\mathrm{CO})_{5}\right]^{+}
  • (d) \left[\mathrm{V}(\mathrm{CO})_{6}\right]^{-}
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Answer: (b)

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Q90 · 2012 · 2 marks

The complex that DOES NOT obey 18- electron rule is:
  • (a) [(\eta^5\text{-}\mathrm{C_5H_5})\mathrm{RuCl(CO)(PPh_3)}]
  • (b) [\mathrm{W(CO)_3(SiMe_3)(Cl)(NCMe)_2}]
  • (c) [\mathrm{IrCl_3(PPh_3)_2(AsPh)_2}]^{-}
  • (d) [\mathrm{Os(N)Br_2(PMe_3)(NMe_2)}]^{-}
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Answer: (d)

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Q91 · Dec 2012 · 2 marks

In hydrofomylation reaction using \mathrm{[Rh(PPh_3)_2(CO)(H)]} as the catalyst, addition of excess \mathrm{PPh_3}, would
  • (a) increase the rate of reaction
  • (b) decrease the rate of reaction.
  • (c) not influence of the rate of reaction
  • (d) stop the reaction.
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Answer: (b)

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Q92 · 2012 · 2 marks

The reactions of \mathrm{Ni}(\mathrm{CO})_{4} with the ligand \left(\mathrm{L}=\mathrm{PMe}_{3}\right. or \left.\mathrm{P}(\mathrm{OMe})_{3}\right) \mathrm{L} yields \mathrm{Ni}(\mathrm{CO})_{3} \mathrm{~L}. The reaction is
  • (a) Associative
  • (b) Dissociative
  • (c) Interchange \left(\mathrm{I}_{\mathrm{a}}\right)
  • (d) Interchange \left(\mathrm{I}_{\mathrm{d}}\right)
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Answer: (b)

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Q93 · 2012 · 2 marks

Among the following the strongest oxidizing agent is:
  • (a) \left[\mathrm{WO}_{4}\right]^{-2}
  • (b) \left[\mathrm{CrO}_{4}\right]^{-2}
  • (c) \left[\mathrm{MoO}_{4}\right]^{-2}
  • (d) \left[\mathrm{ReO}_{4}\right]^{-2}
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Answer: (b)

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Q94 · 2012 · 2 marks

For the reaction, trans- \left[\mathrm{IrCl}(\mathrm{CO})\left(\mathrm{PPh}_{3}\right)_{2}\right]+\mathrm{Cl}_{2} \rightarrow trans -\left[\mathrm{IrCl}_{3}(\mathrm{CO})\left(\mathrm{PPh}_{3}\right)_{2}\right] the correct observation
  • (a) \bar{v} \operatorname{co} (product) >\bar{v} \operatorname{co} (reactant)
  • (b) \bar{v} \operatorname{co} (product) <\bar{v} \operatorname{co} (reactant)
  • (c) \bar{v} \operatorname{co} (product) =\bar{v} \operatorname{co} (reactant)
  • (d) \bar{v} \operatorname{co}( product )=\bar{v} \operatorname{co}( free CO)
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Answer: (a)

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Q95 · June 2012 · 2 marks

The cluster having arachno type structure is:
  • (a) \left[\mathrm{Os}_{5}(\mathrm{CO})_{16}\right]
  • (b) \left[\mathrm{Os}_{3}(\mathrm{CO})_{12}\right]
  • (c) \left[\operatorname{Ir}_{4}(\mathrm{CO})_{12}\right]
  • (d) \left[\mathrm{Rh}_{6}(\mathrm{CO})_{16}\right]
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Answer: (b)

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Q96 · 2012 · 2 marks

The final product of the reaction \left[\mathrm{Mn}(\mathrm{CO})_{6}\right]^{+}+\mathrm{MeLi} \rightarrow is:
  • (a) \left[\mathrm{Mn}(\mathrm{CO})_{6}\right]^{+} \mathrm{Me}^{-}
  • (b) \left[\mathrm{Mn}(\mathrm{CO})_{5} \mathrm{Me}\right]
  • (c) \left[\mathrm{Mn}(\mathrm{CO})_{6}\right]
  • (d) \left[(\mathrm{MeCO}) \mathrm{Mn}(\mathrm{CO})_{5}\right]
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Answer: (d)

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Q97 · Dec 2012 · 2 marks

The substitution of \eta^{5}-\mathrm{Cp} group with nitric oxide is the easiest for
  • (a) \left(\eta^{5}-\mathrm{Cp}_{2}\right) \mathrm{Fe}
  • (b) \left(\eta^{5}-\mathrm{Cp}_{2}\right) \mathrm{CoCl}
  • (c) \left(\eta^{5}-\mathrm{Cp}_{2}\right) \mathrm{Ni}
  • (d) \left(\eta^{5}-\mathrm{Cp}_{2}\right) \mathrm{Co}
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Answer: (c)

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Q98 · Dec 2012 · 2 marks

In the cluster \left[\mathrm{Co}_{3}(\mathrm{CH})(\mathrm{CO})_{9}\right] obeying 18e rule, the number of metal-metal bonds and the bridging ligands respectively, are
  • (a) 3 and 1 CH
  • (b) 0 and 3 CO
  • (c) 3 and 1 CO
  • (d) 6 and 1 CH
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Answer: (a)

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Q99 · Dec 2012 · 2 marks

Which one of the following will NOT undergo oxidative addition by methyl iodide?
  • (a) \left[\mathrm{Rh}(\mathrm{CO})_{2} \mathrm{I}_{2}\right]^{-}
  • (b) \left[\operatorname{Ir}\left(\mathrm{PPh}_{3}\right)_{2}(\mathrm{CO}) \mathrm{Cl}\right]
  • (c) \left[\left(\eta^{2}-\mathrm{CpRu}(\mathrm{CO})_{2}\right]\right.
  • (d) \left[\left(\eta^{5}-\mathrm{C} \mathrm{p}_{2} \mathrm{Ti}(\mathrm{Me}) \mathrm{Cl}\right]\right.
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Answer: (d)

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Q100 · Dec 2012 · 2 marks

In hydrofomylation reaction using \left[\mathrm{Rh}\left(\mathrm{PPh}_{3}\right)_{2}(\mathrm{CO})(\mathrm{H})\right] as the catalyst, addition of excess \mathrm{PPh}_{3}, would
  • (a) increase the rate of reaction
  • (b) decrease the rate of reaction.
  • (c) not influence of the rate of reaction
  • (d) stop the reaction.
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Answer: (b)

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Q101 · June 2011 · 2 marks

The oxidative addition and reductive elimination steps are favoured by
  • (a) Electron rich metal centres.
  • (b) Electron deficient metal centers
  • (c) Electron deficient and electron rich metal centers respectively.
  • (d) Electron rich and electron deficient metal centers respectively
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Answer: (d)

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Q102 · June 2011 · 2 marks

Oxidation occurs very easily in case of
  • (a) \mathrm{(\eta^5\text{-}C_5H_5)_2Fe}
  • (b) \mathrm{(\eta^5\text{-}C_5H_5)_2Co}
  • (c) \mathrm{(\eta^5\text{-}C_5H_5)_2Ru}
  • (d) \mathrm{(\eta^5\text{-}C_5H_5)_2Co^+}
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Answer: (b)

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Q103 · 2011 · 2 marks

In the trans-\mathrm{PtCl_2L(CO)} complex, the CO stretching frequency for L = \mathrm{NH_3}, pyridine, \mathrm{NMe_3} decreases in the order.
  • (a) pyridine > \mathrm{NH_3} > \mathrm{NMe_3}
  • (b) \mathrm{NH_3} > pyridine > \mathrm{NMe_3}
  • (c) \mathrm{NMe_3} > \mathrm{NH_3} > pyridine
  • (d) pyridine > \mathrm{NMe_3} > \mathrm{NH_3}
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Answer: (a)

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Q104 · June 2011 · 2 marks

Identify the order according to increasing stability of the following organometallic \mathrm{TiMe}_{4}, \mathrm{Ti}\left(\mathrm{CH}_{2} \mathrm{Ph}\right)_{4}, \mathrm{Ti}(\mathrm{i}-\mathrm{Pr})_{4}, and \mathrm{TiEt}_{4}(\mathrm{Me}= methyl, \mathrm{Ph}= phenyl, i-Pr = isopropyl, \mathrm{Et}= ethyl )
  • (a) \mathrm{Ti}\left(\mathrm{CH}_{2} \mathrm{Ph}\right)_{4}<\mathrm{Ti}(\mathrm{i}-\mathrm{pr})_{4}<\mathrm{TiEt}_{4}<\mathrm{TiMe}_{4}
  • (b) \mathrm{TiEt}_{4}<\mathrm{TiMe}_{4}<\mathrm{Ti}(\mathrm{i}-\mathrm{Pr})_{4}<\mathrm{Ti}\left(\mathrm{CH}_{2} \mathrm{Ph}\right)_{4}
  • (c) \mathrm{Ti}(\mathrm{i}-\mathrm{Pr})_{4}<\mathrm{TiEt}_{4}<\mathrm{TiMe}_{4}<\mathrm{Ti}\left(\mathrm{CH}_{2} \mathrm{Ph}\right)_{4}
  • (d) \mathrm{TiMe}_{4}<\mathrm{TiEt}_{4}<\mathrm{Ti}(\mathrm{i}-\mathrm{Pr})_{4}<\mathrm{Ti}\left(\mathrm{CH}_{2} \mathrm{Ph}\right)_{4}
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Answer: (c)

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Q105 · Dec 2011 · 2 marks

Among the metals \mathrm{Mn}, \mathrm{Fe}, \mathrm{Co} and Ni , the ones those would react in its native form directly with CO giving metal carbonyl compounds are:
  • (a) Co and Mn
  • (b) Mn and Fe
  • (c) Fe and Ni
  • (d) Ni and Co
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Answer: (c)

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Q106 · June 2011 · 2 marks

In the \mathrm{H}_{2} \mathrm{Ru}_{6}(\mathrm{CO})_{18} cluster, containing 8-coordinated Ru centers, the hydrogen atoms are
  • (a) Both terminal
  • (b) One terminal and the other bridging
  • (c) Both bridging between two Ru centers
  • (d) Both bridging between three Ru centers.
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Answer: (d)

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Q107 · 2011 · 2 marks

The correct combination of metal, number of carbonyl ligands and the charge for a metal carbonyl complex [\mathrm{M}(\mathrm{CO}) \mathrm{x}] \mathrm{z} - that satisfies the 18 electron rule is
  • (a) M=T i, x=6, z=1
  • (b) M=V, x=6, z=1
  • (c) M=C o, x=4, z=2
  • (d) M=M o, x=5, z=1
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Answer: (b)

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Q108 · 2011 · 2 marks

The stable cyclopentadienyl complex of beryllium is
  • (a) \left[\mathrm{Be}\left(\eta^{2}-\mathrm{C}_{5} \mathrm{H}_{5}\right)_{2}\right]
  • (b) \left[\mathrm{Be}\left(\eta^{2}-\mathrm{C}_{5} \mathrm{H}_{5}\right)\left(\eta^{3}-\mathrm{C}_{5} \mathrm{H}_{5}\right)\right]
  • (c) \left[\mathrm{Be}\left(\eta^{1}-\mathrm{C}_{5} \mathrm{H}_{5}\right)\left(\eta^{3}-\mathrm{C}_{5} \mathrm{H}_{5}\right)\right]
  • (d) \left[\mathrm{Be}\left(\eta^{1}-\mathrm{C}_{5} \mathrm{H}_{5}\right)\left(\eta^{5}-\mathrm{C}_{5} \mathrm{H}_{5}\right)\right]
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Answer: (d)

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Q109 · 2011 · 2 marks

Reaction of \mathrm{Fe}(\mathrm{CO})_{5} with \mathrm{OH} leads to complex A which on oxidation with \mathrm{MnO}_{2} gives B. Compounds A and B respectively are
  • (a) [\mathrm{HFe}(\mathrm{CO})_{4}]^{-} and \mathrm{Fe}_{3}(\mathrm{CO})_{12}
  • (b) [\mathrm{Fe}(\mathrm{CO})_{5}(\mathrm{OH})]^{-} and \mathrm{Fe}_{2}(\mathrm{CO})_{10}
  • (c) [\mathrm{Fe}(\mathrm{CO})_{4}]^{-2} and \mathrm{Mn}_{2}(\mathrm{CO})_{10}
  • (d) [\mathrm{HFe}(\mathrm{CO})_{4}]^{-}, and \mathrm{Fe}_{2}\mathrm{O}_{3}
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Answer: (a)

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Q110 · 2011 · 2 marks

The number of metal-metal bonds in the dimers, [\mathrm{CpFe}(\mathrm{CO})(\mathrm{NO})]_{2} and [\mathrm{CpMo}(\mathrm{CO})_{3}]_{2} respectively, are
  • (a) two and two
  • (b) two and three
  • (c) one and two
  • (d) zero and one
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Answer: (d)

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Q111 · Dec 2011 · 2 marks

In the trans- \mathrm{PtCl}_{2} \mathrm{~L}(\mathrm{CO}) complex, the CO stretching frequency for \mathrm{L}=\mathrm{NH}_{3}, pyridine, \mathrm{NMe}_{3} decreases in the order.
  • (a) pyridine >\mathrm{NH}_{3}>\mathrm{NMe}_{3}
  • (b) \mathrm{NH}_{3}> pyridine >\mathrm{NMe}_{3}
  • (c) \mathrm{NMe}_{3}>\mathrm{NH}_{3}> pyridine
  • (d) pyridine >\mathrm{NMe}_{3}>\mathrm{NH}_{3}
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Answer: (a)

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Q112 · 2011 · 2 marks

The greater stability of \left(\left(\mathrm{CH}_{3}\right)_{3} \mathrm{C}-\mathrm{CH}_{2}{ }^{-}\right)_{4} \mathrm{Ti}(\mathrm{A}) compared to that of \left(\left(\mathrm{CH}_{3}\right)_{2} \mathrm{CH}-\mathrm{CH}_{2}{ }^{-}\right)_{4} \mathrm{Ti}(\mathrm{B}) is due to
  • (a) Hyperconjugation present in complex (A)
  • (b) \beta-hydride elimination is not possible in complex (A)
  • (c) Steric protection of titanium from reactive species in complex (A)
  • (d) The stronger nature of Ti-C bond in complex (A).
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Answer: (b)

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Questions from the ABC Question Bank, typed from the official papers. A question whose answer is still under review is not shown.

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