Q1 · June 2021 · 2 marks
Which of the following statements regarding dissociative substitution in an octahedral transition metal complex, (1) High steric hindrance between ligands in the metal complex favours fast dissociation of ligand. (2) Increased charge on the metal atom/ion of the complex favours the acceptance of electron pair of the entering ligands. (3) A penta-coordinated intermediate is observed. (4) Nature of the entering ligand significantly influences the reaction. Which are correct?
- (a) 1 and 4
- (b) 1 and 3
- (c) 1, 3 and 4
- (d) 1, 2, 3 and 4 22
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Answer: (b)
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Q2 · June 2021 · 2 marks
Consider an octahedral complex Ma2b2cd, where \mathrm{a}, \mathrm{b}, \mathrm{c}, and d are monodentate ligands. The number of enantiomeric pairs for the complex is
- (a) one
- (b) two
- (c) three
- (d) four
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Answer: (b)
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Q3 · June 2021 · 2 marks
For the ligand-to-metal charge-transfer (LMCT) transitions in the oxo-anions given below, the wavelength of the transitions are in the order
- (a) \mathrm{VO}_{4}^{3-}<\mathrm{CrO}_{4}^{2-}<\mathrm{MnO}_{4}^{-}and \mathrm{WO}_{4}^{2-}<\mathrm{MoO}_{4}^{2-}<\mathrm{CrO}_{4}^{2-}
- (b) \mathrm{VO}_{4}^{3-}<\mathrm{CrO}_{4}^{2-}<\mathrm{MnO}_{4}^{-}and \mathrm{WO}_{4}^{2-}>\mathrm{MoO}_{4}^{2-}>\mathrm{CrO}_{4}^{2-}
- (c) \mathrm{VO}_{4}^{3-}>\mathrm{CrO}_{4}^{2-}>\mathrm{MnO}_{4}^{-}and \mathrm{WO}_{4}^{2-}<\mathrm{MoO}_{4}^{2-}<\mathrm{CrO}_{4}^{2-}
- (d) \mathrm{VO}_{4}^{3-}>\mathrm{CrO}_{4}^{2-}>\mathrm{MnO}_{4}^{-}and \mathrm{WO}_{4}^{2-}>\mathrm{MoO}_{4}^{2-}>\mathrm{CrO}_{4}^{2-}
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Answer: (a)
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Q4 · June 2021 · 2 marks
Consider the following statements for the self-exchange electron transfer reaction in \left[\mathrm{Cr}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{2+/ 3+}
- (a) \sigma^{*} orbitals are only involved in electron transfer
- (b) It involves large inner-sphere reorganization energy
- (c) It involves no change in M-L bond lengths
- (d) Rate of self-exchange electron transfer is fast
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Answer: (b)
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Q5 · June 2021 · 2 marks
The number of CO bands for isomers from sets (i) and (ii) in their IR spectra Set (i): Trigonal bipyramidal isomers, axial- \mathrm{Fe}(\mathrm{CO})_{4} \mathrm{~L}(\mathrm{~A}) and equatorial- \mathrm{Fe}(\mathrm{CO})_{4} \mathrm{~L}(\mathrm{~B}) Set (ii): Octahedral isomers, fac- \mathrm{Mo}(\mathrm{CO})_{3} \mathrm{~L}_{3}(\mathrm{C}) and mer- \mathrm{Mo}(\mathrm{CO})_{3} \mathrm{~L}_{3}(\mathrm{D}) are
- (a) A, 4 and B, 3; C, 3 and D, 2
- (b) A, 4 and B, 3; C, 2 and D, 3
- (c) A, 3 and B, 4; C, 3 and D, 2
- (d) A, 3 and B, 4; C, 2 and D, 3
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Answer: (d)
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Q6 · June 2021 · 2 marks
The absorption spectrum of \left[\mathrm{Cr}\left(\mathrm{NH}_{3}\right)_{6}\right]^{3+} in water shows two bands around 475 and 365 nm . The ground term and the spin-allowed transitions, respectively, are
- (a) { }^{4} \mathrm{~F} ;{ }^{4} \mathrm{~T}_{1 \mathrm{~g}}(\mathrm{~F}) \rightarrow{ }^{4} \mathrm{~T}_{2 \mathrm{~g}} and { }^{4} \mathrm{~T}_{1 \mathrm{~g}} \rightarrow{ }^{4} \mathrm{~A}_{2 \mathrm{~g}}
- (b) { }^{4} \mathrm{~F} ;{ }^{4} \mathrm{~A}_{2 \mathrm{~g}} \rightarrow{ }^{4} \mathrm{~T}_{2 \mathrm{~g}} and { }^{4} \mathrm{~A}_{2 \mathrm{~g}} \rightarrow{ }^{4} \mathrm{~T}_{1 \mathrm{~g}}(\mathrm{~F})
- (c) { }^{2} \mathrm{G} ;{ }^{2} \mathrm{Eg} \rightarrow{ }^{2} \mathrm{~T}_{1 \mathrm{~g}} and { }^{2} \mathrm{Eg}_{\mathrm{g}} \rightarrow{ }^{2} \mathrm{~T}_{1 \mathrm{~g}}
- (d) { }^{2} \mathrm{~F} ;{ }^{4} \mathrm{~A}_{2 \mathrm{~g}} \rightarrow{ }^{2} \mathrm{~T}_{2 \mathrm{~g}} and { }^{2} \mathrm{~A}_{2 \mathrm{~g}} \rightarrow{ }^{2} \mathrm{~T}_{1 \mathrm{~g}}(\mathrm{~F})
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Answer: (b)
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Q7 · June 2021 · 2 marks
For trigonal bipyramidal coordination complex (ML5) the correct point group symmetry and the relative order of the energies of the 3d orbitals in that crystal field, respectively are
- (a) \mathrm{D}_{3 \mathrm{~h}} ; \mathrm{d}_{\mathrm{x} 2-\mathrm{y} 2}>\mathrm{d}_{\mathrm{z} 2},>\mathrm{d}_{\mathrm{xy}}>\mathrm{d}_{\mathrm{xz}}, \mathrm{d}_{\mathrm{yz}}
- (b) \mathrm{D}_{3 \mathrm{~d}} ; \mathrm{d}_{\mathrm{z}} 2,>\mathrm{d}_{\mathrm{xy}}, \mathrm{d}_{\mathrm{x} 2-\mathrm{y} 2}>\mathrm{d}_{\mathrm{xz}}, \mathrm{d}_{\mathrm{yz}}
- (c) \mathrm{D}_{3 \mathrm{~d}} ; \mathrm{d}_{\mathrm{x} 2-\mathrm{yz}}>\mathrm{d}_{\mathrm{zz}}, \mathrm{d}_{\mathrm{xy}}>\mathrm{d}_{\mathrm{xz}}, \mathrm{d}_{\mathrm{yz}}
- (d) \mathrm{D}_{3 \mathrm{~h}} ; \mathrm{d}_{\mathrm{z} 2},>\mathrm{d}_{\mathrm{x} 2-\mathrm{y} 2}, \mathrm{dxy}>\mathrm{d}_{\mathrm{xz}}, \mathrm{d}_{\mathrm{yz}} COORDINATION CHEMISTRY
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Answer: (d)
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Q8 · 2020 · 2 marks
Consider the following statements:
- (a) \mathbf{C r}^{+2} is easier to oxidize than \mathbf{V}^{+2} in the gas phase
- (b) \mathbf{C r}^{+2} (aq) is a more powerful reducing agent than \mathbf{V}^{+2} (aq).
- (c) The rate of water exchange for \mathbf{C r}^{+2}(\mathbf{a q}) is much faster than for \mathbf{V}^{+2}(\mathbf{a q})
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Answer: (c)
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Q9 · 2020 · 2 marks
\mathrm{I}_{2} is violet in the solid as well as in gas phase. However in acetone or ethanol, it turns brown. Choose the correct statement(s) for this colour change:
- (a) Dissociation of \mathbf{I}_{\mathbf{2}} in atomic state
- (b) Interaction of low-lying \sigma^{*}-orbital of iodine with lone pair of O (solvent)
- (c) Formation of a charge-transfer complex [CSIR-2020] 1(a) only 2(b) only 3(a) and (b) only 4(b) and (c) only
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Answer: (d)
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Q10 · 2020 · 2 marks
The pair of compounds in which both members show LMCT band in their electronic spectra is [CSIR-2020]
- (a) \left[\mathrm{FeCl}_{4}\right]^{-2} and \left[\mathrm{Fe}(\mathrm{bpy})_{3}\right]^{+2}
- (b) \left[\mathrm{FeBr}_{4}\right]^{-2} and \left[\mathrm{TcO}_{4}\right]^{-}
- (c) \left[\mathrm{ReO}_{4}\right]^{-}and [\mathrm{Ru}(\mathrm{bpy})]^{+2}
- (d) \left[\mathrm{Fe}(\mathrm{phen})_{3}\right]^{+2} and \left[\mathrm{FeCl}_{4}\right]^{-2}
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Answer: (b)
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Q11 · 2020 · 2 marks
For the \mathrm{d}^{3} electron configuration, the ground state term symbol is
- (a) { }^{4} \mathrm{~F}_{1 / 2}
- (b) { }^{4} \mathrm{~F}_{3 / 2}
- (c) { }^{4} \mathrm{~F}_{7 / 2}
- (d) { }^{4} \mathrm{~F}_{9 / 2}
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Answer: (b)
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Q12 · 2020 · 2 marks
The value of magnetic moment will be independent of temperature for(acac = acetylacetonato; OAc = acetate; o-phen = o-phenathroline; Pz = pyrazolyl)
- (a) \left[\mathrm{Fe}(\mathrm{acac})_{3}\right]
- (b) \left[\mathrm{Cu}(\mathrm{OAc})_{4}\left(\mathrm{H}_{2} \mathrm{O}\right)_{2}\right]
- (c) \left[\mathrm{Fe}(\text { o-phen })_{2}(\mathrm{NCS})_{2}\right]
- (d) \left[\mathrm{Fe}\left\{\left(\mathrm{HC}\left(3,5-\mathrm{Me}_{2} \mathrm{Pz}\right)_{3}\right\}_{2}\right]_{+2}\right.
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Answer: (a)
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Q13 · 2020 · 2 marks
In the following sequence of reactions the correct P, Q and R are respectively 

- (a) \mathrm{KNO}_{2}, \mathrm{CO}_{2},\left[\mathrm{Fe}\left(\mathrm{H}_{2} \mathrm{O}\right)_{5} \mathrm{~S}\right]^{+}, \mathrm{HgS}
- (b) \mathrm{KNO}_{2}, \mathrm{~N}_{2},\left[\mathrm{Fe}\left(\mathrm{H}_{2} \mathrm{O}\right)_{5}(\mathrm{SCN})\right]^{2+},\left[\mathrm{Hg}(\mathrm{SCN})_{4}\right]^{2-}
- (c) \mathrm{KNO}_{3}, \mathrm{~N}_{2},\left[\mathrm{Fe}\left(\mathrm{H}_{2} \mathrm{O}\right)_{5}(\mathrm{CN})\right]^{+2},\left[\mathrm{Hg}(\mathrm{OCN})_{4}\right]^{2-}
- (d) \mathrm{NaN}_{3}, \mathrm{~N}_{2},\left[\mathrm{Fe}\left(\mathrm{H}_{2} \mathrm{O}\right)_{5}(\mathrm{~N} 3)\right]^{+2},\left[\mathrm{Hg}\left(\mathrm{N}_{3}\right) 4\right]^{2-}
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Answer: (b)
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Q14 · 2019 · 2 marks
Hydrolysis of trans-\mathrm{[CoLCl(en)_2]^+} (\mathrm{L = NO_2^-, NCS^-, OH^-, Cl^-}) results in a product (A). The tendency to form cis-isomer of the product (A) follows the order [CSIR-JUNE 2019]
- (a) \mathrm{L = NO_2^- < NCS^- < OH^- < Cl^-}
- (b) \mathrm{L = NO_2^- < Cl^- < NCS^- < OH^-}
- (d) \mathrm{L = OH^- < NCS^- < Cl^- < NO_2^-}
- (c) \mathrm{L = OH^- < Cl^- < NO_2^- < NCS^-}
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Answer: (b)
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Q15 · 2019 · 2 marks
Donor mode of NO ligand depends on the metal. Now, consider the following complexes (in gaseous state). (A) \mathrm{[IrCl(CO)(PPh_3)_2(NO)]^+} (B) \mathrm{[RuCl(PPh_3)_2(NO)_2]^+} (C) \mathrm{[Co(NCS)(diars)_2(NO)]^+}, where diars \rightarrow o-\mathrm{(Me_2As)_2C_6H_4}. (D) \mathrm{[Cr(CN)_5(NO)]^{3-}} The complex(es) that do NOT exhibit bent NO coordination mode is/are [CSIR-JUNE 2019]
- (a) A and B
- (b) C and D
- (c) D only
- (d) B only
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Answer: (c)
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Q16 · 2019 · 2 marks
\mathrm{FeCr_2O_4} and \mathrm{NiGa_2O_4} have normal and inverse spinel structures, respectively. The correct statement is [CSIR-DEC 2019]
- (a) Fe(II) and Ni(II) occupy octahedral sites
- (b) Fe(II) and Ni(II) occupy tetrahedral and octahedral sites, respectively
- (c) Cr(III) and Ga(III) occupy only octahedral sites
- (d) Cr(III) and Ga(III) occupy tetrahedral and octahedral sites, respectively
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Answer: (b)
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Q17 · June 2019 · 2 marks
Self-exchange electron transfer is fastest in
- (a) \left[\mathrm{Ru}\left(\mathrm{NH}_{3}\right)_{6}\right]^{+2 /+3}
- (b) \left[\mathrm{Co}\left(\mathrm{NH}_{3}\right)_{6}\right]^{+2 /+3}
- (c) \left[\mathrm{Cr}(\mathrm{OH})_{6}\right]^{+2 /+3}
- (d) \left[\mathrm{Fe}\left(\mathrm{OH}_{2}\right)_{6}\right]^{+2 /+3}
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Answer: (a)
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Q18 · June 2019 · 2 marks
Consider the following reaction: \mathrm{Hg}^{+2}(\mathrm{aq})+\mathrm{X}^{-}(\mathrm{aq})=[\mathrm{HgX}]^{+}(\mathrm{aq})
The stability constants for [\mathrm{HgX}]^{+}(\mathrm{aq}) for \mathrm{X}=\mathrm{F}, \mathrm{Cl} and Br follow the order - (a) \mathrm{F}<\mathrm{Cl}<\mathrm{Br}
- (b) \mathrm{Br}<\mathrm{Cl}<\mathrm{F}
- (c) \mathrm{Cl}<\mathrm{Br}<\mathrm{F}
- (d) \mathrm{Br}<\mathrm{F}<\mathrm{Cl}
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Answer: (a)
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Q19 · June 2019 · 2 marks
Consider the following statements regarding electronic spectra of high spin complexes
- (a) \mathrm{Ti}^{+3} complexes exhibit one sharp band.
- (b) \mathrm{Co}^{+2} and \mathrm{Cr}+3 complexes exhibit two broad bands.
- (c) \mathrm{Mn}^{+2} complexes exhibit a series of very weak and sharp bands.
- (d) \mathrm{Ni}^{+2} complexes exhibit three broad bands .
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Answer: (c)
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Q20 · June 2019 · 2 marks
Donor mode of NO ligand depends on the metal. Now, consider the following complexes (in gaseous state).
- (a) \left[\mathrm{IrCl}(\mathrm{CO})\left(\mathrm{PPh}_{3}\right)_{2}(\mathrm{NO})\right]^{+} A and B
- (b) \left[\mathrm{RuCl}\left(\mathrm{PPh}_{3}\right)_{2}(\mathrm{NO})_{2}\right]+ C and D
- (c) \left[\mathrm{Co}(\mathrm{NCS})(\text { diars })_{2}(\mathrm{NO})\right]^{+}, where diars \rightarrow \mathrm{o}-\left(\mathrm{Me}_{2} \mathrm{As}\right)_{2} \mathrm{C}_{6} \mathrm{H}_{4}. D only
- (d) \left[\mathrm{Cr}(\mathrm{CN})_{5}(\mathrm{NO})\right]^{3-} The complex (es) that do NOT exhibit bent NO coordination mode is/are B only
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Answer: (c)
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Q21 · 2019 · 2 marks
An aqueous solution of metal ion (A) gives a blood-red colored product (B) upon reaction with KSCN. Upon dropwise addition of NaF, the complex turns to a colorless compound (C). Identify A,B and C [CSIR-JUNE 2019]
- (a) aq. \mathrm{Fe}(\mathrm{II}),\left[\mathrm{Fe}(\mathrm{SCN})\left(\mathrm{H}_{2} \mathrm{O}\right)_{5}\right]^{+}and \left[\mathrm{Fe}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{+2}
- (b) aq. \mathrm{Fe}(\mathrm{III}),\left[\mathrm{Fe}(\mathrm{SCN})\left(\mathrm{H}_{2} \mathrm{O}\right)_{5}\right]^{+2} and \left[\mathrm{FeF}_{6}\right]^{+3}
- (c) aq. \mathrm{Fe}(\mathrm{II}),\left[\mathrm{Fe}(\mathrm{SCN})\left(\mathrm{H}_{2} \mathrm{O}\right)_{5}\right]^{+}and \mathrm{FeF}_{3}
- (d) aq. \mathrm{Fe}(\mathrm{III}),\left[\mathrm{Fe}(\mathrm{SCN})_{3}\left(\mathrm{H}_{2} \mathrm{O}\right)_{3}\right]^{+}and \mathrm{FeF}_{3}
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Answer: (b)
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Q22 · June 2019 · 2 marks
Correct order of molar extinction coefficient values of the visible absorption bands for the following species is
- (a) \left[\mathrm{Cr}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{+2}>\left[\mathrm{Mn}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{+2}> Chlorophyll >\left[\mathrm{NiCl}_{4}\right]^{-2}
- (b) Chlorophyll >\left[\mathrm{NiCl}_{4}\right]^{-2}>\left[\mathrm{Cr}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{+2}>\left[\mathrm{Mn}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{+2}
- (c) \left[\mathrm{NiCl}_{4}\right]^{-2}> Chlorophyll >\left[\mathrm{Cr}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{+2}>\left[\mathrm{Mn}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{+2}
- (d) \mathrm{Chlorophyll}>\left[\mathrm{Cr}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{+2}>[\mathrm{NiCl}]^{-2}>\left[\mathrm{Mn}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{+2}
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Answer: (b)
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Q23 · June 2019 · 2 marks
The correct statement about base hydrolysis of \left[\mathrm{Co}(\mathrm{py})_{4} \mathrm{Cl}_{2}\right]^{+}(py-pyridine) is
- (a) rate expression is, Rate- \mathrm{k}\left[\mathrm{Co}(\mathrm{py})_{4} \mathrm{Cl}_{2}\right]^{+}\left[\mathrm{OH}^{-}\right]
- (b) reaction does not depend on hydroxide ion concentration
- (c) reaction proceeds through \mathrm{S}_{\mathrm{N} 1} \mathrm{CB} mechanism
- (d) intermediate involved in this reaction is \left[\mathrm{Co}(\mathrm{py})_{4} \mathrm{Cl}_{2}(\mathrm{OH})\right]
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Answer: (b)
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Q24 · June 2019 · 2 marks
\mathrm{FeCr}_{2} \mathrm{O}_{4} and \mathrm{NiGa}_{2} \mathrm{O}_{4} have normal and inverse spinel structures, respectively. The correct statement is
- (a) Fe(II) and Ni(II) occupy octahedral sites
- (b) Fe (II) and Ni(II) occupy tetrahedral and octahedral sites, respectively
- (c) Cr(III) and Ga(III) occupy only octahedral sites
- (d) Cr(III) and Ga(III) occupy tetrahedral and octahedral sites, respectively
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Answer: (b)
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Q25 · June 2019 · 2 marks
The correct match of spin-only magnetic moment for the complexes cis- \left[\mathrm{Fe}(\mathrm{phen})_{2}(\mathrm{NCS}-\mathrm{N})_{2}\right]
- (a) and \left[\mathrm{Fe}(\text { phen })_{3}\right] \mathrm{Cl}_{2}(\mathrm{~B}) at 300 K is (phen =1,10-phenantholine) 4.89 BM for both A and B
- (b) 0 BM for both A and B
- (c) 4.89 BM for A and 0 BM for B
- (d) 0 BM for A and 4:59 BM for B 20
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Answer: (c)
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Q26 · June 2019 · 2 marks
In the electronic spectrum of \left[\mathrm{IrBr}_{6}\right]^{2-}, the number of charge transfer band(s) and their origin are respectively
- (a) Two ligand \rightarrow metal \left(\sigma \rightarrow \mathrm{t}_{2 \mathrm{~g}}\right. and \left.\sigma \rightarrow \mathrm{a}_{1 \mathrm{~g}}{ }^{*}\right)
- (b) One ligand → metal \left(\sigma \rightarrow \mathrm{e}_{\mathrm{g}}\right)
- (c) Two ligand → metal \left(\sigma \rightarrow \mathrm{t}_{2 \mathrm{~g}}\right. and \left.\sigma \rightarrow \mathrm{e}_{\mathrm{g}}\right)
- (d) One ligand → metal \left(\sigma \rightarrow \mathrm{t}_{2 \mathrm{~g}}\right)
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Answer: (c)
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Q27 · June 2019 · 2 marks
The number of geometrical isomers of the complex \left[\mathrm{RhH}(\mathrm{C} \equiv \mathrm{CR})_{2}\left(\mathrm{PMe}_{3}\right)_{3}\right] is
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Answer: (b)
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Q28 · June 2019 · 2 marks
The calculated heat of formation \left(\Delta \mathrm{H}_{\mathrm{f}}\right) for \mathrm{NaCl}_{2} and CaF is
- (a) negative for both \mathrm{NaCl}_{2} and CaF
- (b) negative for \mathrm{NaCl}_{2} but positive for CaF
- (c) positive for \mathrm{NaCl}_{2} but negative for CaF
- (d) positive for both \mathrm{NaCl}_{2} and CaF
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Answer: (c)
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Q29 · 2018 · 2 marks
Consider the following reaction: \mathrm{Hg^{+2}(aq) + X^{-}(aq) = [HgX]^{+}(aq)}
The stability constants for [\mathrm{HgX}]^{+}(\mathrm{aq}) for X = F, Cl and Br follow the order [CSIR-JUNE 2019] - (a) F < Cl < Br
- (b) Br < Cl < F
- (c) Cl < Br < F
- (d) Br < F < Cl
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Answer: (a)
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Q30 · June 2018 · 2 marks
The total degeneracy of the ground term of \mathrm{Co^{II}} (high spin) in octahedral geometry is
- (a) 18
- (b) 12
- (c) 28
- (d) 9
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Answer: (c)
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Q31 · June 2018 · 2 marks
The lowest energy state of a 1 \mathrm{~s}^{1} 2 \mathrm{~s}^{1} electronic configuration, according to hund's rule, is
- (a) { }^{3} \mathrm{~S}_{0}
- (b) { }^{1} \mathrm{~S}_{0}
- (c) { }^{3} \mathrm{~S}_{1}
- (d) { }^{1} \mathrm{~S}_{1}
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Answer: (c)
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Q32 · June 2018 · 2 marks
Consider the following statements:
- (a) \mathrm{Cr}^{+2} is easier to oxidize than \mathrm{V}^{+2} in the gas phase
- (b) \mathrm{Cr}^{+2}(\mathrm{aq}) is a more powerful reducing agent than \mathrm{V}^{+2}(\mathrm{aq}).
- (c) The rate of water exchange for \mathrm{Cr}^{+2}(\mathrm{aq}) is much faster than for \mathrm{V}^{+2}(\mathrm{aq})
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Answer: (c)
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Q33 · June 2018 · 2 marks
The allowed electronic transition in fluorine molecule is
- (a) \sum_{\mathrm{g}}^{+} \rightarrow \sum_{\mathrm{g}}^{+}
- (b) \sum_{\mathrm{g}}^{+} \rightarrow \sum_{\mathrm{g}}^{+}
- (c) \sum_{\mathrm{g}}^{+} \rightarrow \pi_{\mathrm{u}}
- (d) \sum_{\mathrm{g}}^{+} \rightarrow \Delta_{\mathrm{u}}
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Answer: (c)
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Q34 · 2018 · 2 marks
Consider the species \mathrm{NO}, \mathrm{I}_{2}, \mathrm{I}_{2}^{-}, \mathrm{Cu}^{+2} and \mathrm{VO}^{+2}. The number of paramagnetic species among them and the EPR inactive species, respectively, are
- (a) 4 and \mathrm{I}_{2}{ }^{-}
- (b) 4 and \mathrm{I}_{2}
- (c) 3 and \mathrm{VO}^{+2}, \mathrm{Cu}^{+2}
- (d) 3 and \mathrm{NO}, \mathrm{Cu}^{+2}
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Answer: (b)
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Q35 · 2018 · 2 marks
The correct set of electronic configurations for metal ions in octahedral coordination geometry for strong Jahn-Teller distortion is
- (a) \mathrm{t}^{6}{ }_{2 \mathrm{~g}} \mathrm{e}^{1}{ }_{\mathrm{g}}, \mathrm{t}^{3}{ }_{2 \mathrm{~g}} \mathrm{e}^{1}{ }_{\mathrm{g}}, \mathrm{t}^{6}{ }_{2 \mathrm{~g}} \mathrm{e}^{3}{ }_{\mathrm{g}}
- (b) \mathrm{t}^{1}{ }_{2 \mathrm{~g}}, \mathrm{t}^{3}{ }_{2 \mathrm{~g}} \mathrm{e}^{2}{ }_{\mathrm{g}}, \mathrm{t}^{6}{ }_{2 \mathrm{~g}} \mathrm{e}^{1}{ }_{\mathrm{g}}
- (c) \mathrm{t}^{3}{ }_{2 \mathrm{~g}}, \mathrm{t}^{3}{ }_{2 \mathrm{~g}} \mathrm{e}^{1}{ }_{\mathrm{g}}, \mathrm{t}^{3}{ }_{2 \mathrm{~g}} \mathrm{e}^{2}{ }_{\mathrm{g}}
- (d) \mathrm{t}^{3}{ }_{2 \mathrm{~g}} \mathrm{e}^{2}{ }_{\mathrm{g}}, \mathrm{t}^{6}{ }_{2 \mathrm{~g}} \mathrm{e}^{2}{ }_{\mathrm{g}}, \mathrm{t}^{6}{ }_{2 \mathrm{~g}} \mathrm{e}^{3}{ }_{\mathrm{g}}
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Answer: (a)
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Q36 · 2018 · 2 marks
Consider the two sets of molecules. Set A: \left[\mathrm{AIF}_{6}\right]^{-3},\left[\mathrm{PF}_{6}\right]^{-},\left[\mathrm{SF}_{6}\right] and \left[\mathrm{SiF}_{6}\right]^{-2} Set \mathrm{B}:\left[\mathrm{Ba}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{+2},\left[\mathrm{Ca}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{+2},\left[\mathrm{Mg}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{+2},\left[\mathrm{Sr}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{+2} The slowest ligand exchange rate in Set A and Set B are, respectively [CSIR-DEC 2018]
- (a) \left[\mathrm{AIF}_{6}\right]^{-3} and \left[\mathrm{Sr}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{+2}
- (c) \left[\mathrm{SiF}_{6}\right]^{-2} and \left[\mathrm{Ca}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{+2}
- (b) \left[\mathrm{SF}_{6}\right] and \left[\mathrm{Mg}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{+2}
- (d) \left[\mathrm{PF}_{6}\right]^{-}and \left[\mathrm{Ca}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{+2}
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Answer: (b)
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Q37 · 2017 · 2 marks
The geometry around Cu and its spin state for \mathrm{K_3CuF_6} and \mathrm{KCuL_2}, [\mathrm{H_2L = H_2NCONHCONH_2}], respectively are: [CSIR-DEC 2017]
- (a) (octahedral, high-spin) and (square planar, low-spin)
- (b) (octahedral, low-spin) and (square planar, low-spin)
- (c) (trigonal prismatic, high-spin) and (tetrahedral, high-spin)
- (d) (trigonal prismatic, low-spin) and (tetrahedral, high-spin)
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Answer: (a)
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Q38 · 2017 · 2 marks
For high spin and low spin d^{6} octahedral complexes (\mathrm{ML_6}), the generally observed spin allowed transitions respectively, are [CSIR-DEC 2017]
- (a) two and one
- (b) one and two
- (c) zero and one
- (d) two and two
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Answer: (b)
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Q39 · 2017 · 2 marks
\mathrm{Br_2} with propanone forms a charge transfer complex and \mathrm{I_2} forms triiodide anion with \mathrm{I^-}. This implies that [CSIR-DEC 2017]
- (a) both \mathrm{Br_2} and \mathrm{I_2} act as bases
- (b) both \mathrm{Br_2} and \mathrm{I_2} act as acids
- (c) \mathrm{Br_2} acts as an acid and \mathrm{I_2} acts as a base
- (d) \mathrm{Br_2} acts as a base and \mathrm{I_2} acts an an acid
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Answer: (b)
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Q40 · 2016 · 2 marks
\mathrm{CdS}, \mathrm{HgS} and BiI 3 are coloured due to
- (a) L→M charge transfer transitions
- (b) d → d electronic transitions
- (c) M→L charge transfer transitions
- (d) combination of \mathrm{L} \rightarrow \mathrm{M} charge transfer and \mathrm{d} \rightarrow \mathrm{d} electronic transitions
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Answer: (a)
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Q41 · June 2017 · 2 marks
The relative rates of water exchange for the hydrated complexes of (1) \mathrm{Ni}^{+2} (2) \mathrm{V}^{+2} and (3) \mathrm{Cr}^{3}+ ions follows the trend:
- (a) (1)>(2)>(3)
- (b) (1)<(2)<(3)
- (c) (1)>(2)<(3)
- (d) (1)<(2)>(3)
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Answer: (a)
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Q42 · 2017 · 2 marks
For the following complexes, the increasing order of magnetic moment (spin only value) is
A. [\mathrm{TiF}_6]^{-3}
B. [\mathrm{CrF}_6]^{-3}
C. [\mathrm{MnF}_6]^{-3}
D. [\mathrm{CoF}_6]^{-3}
- (a) D < A < B < C
- (b) C < A < D < B
- (c) B \approx A < D < C
- (d) A < B < C \approx D
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Answer: (d)
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Q43 · Dec 2017 · 2 marks
The geometry around Cu and its spin state for \mathrm{K}_{3} \mathrm{CuF}_{6} and \mathrm{KCuL}_{2}, \left[\mathrm{H}_{2} \mathrm{~L}=\mathrm{H}_{2} \mathrm{NCONHCONH}_{2}\right], respectively are:
- (a) (octahedral, high-spin) and (square planar, low-spin)
- (b) (octahedral, low-spin) and (square planar, low-spin)
- (c) (trigonal prismatic, high-spin) and (tetrahedral, high-spin)
- (d) (trigonal prismatic, low-spin) and (tetrahedral, high-spin)
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Answer: (a)
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Q44 · 2017 · 2 marks
Consider the following statements with respect to the base hydrolysis of \left[\mathrm{CoCl}\left(\mathrm{NH}_{3}\right)_{5}\right] to \left[\mathrm{Co}\left(\mathrm{NH}_{3}\right)_{5}(\mathrm{OH})\right]^{+2}
- (a) One of the ammonia ligands acts as a Bronsted acid.
- (b) The entering group is water.
- (c) A heptacoordinated \mathrm{Co}^{+3} species is an intermediate.
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Answer: (a)
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Q45 · 2016 · 2 marks
The number of microstates present in ^{3}\mathrm{F}-term is [CSIR-JUNE 2016]
- (a) 3
- (b) 21
- (c) 9
- (d) 28
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Answer: (b)
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Q46 · 2016 · 2 marks
The lowest energy term for the d^{6} configuration is [CSIR-JUNE 2016]
- (a) {}^{2}\mathrm{D}
- (b) {}^{5}\mathrm{D}
- (c) {}^{1}\mathrm{P}
- (d) {}^{1}\mathrm{D}
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Answer: (b)
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Q47 · 2016 · 2 marks
The first excited state of hydrogen molecule is [CSIR-JUNE 2016]
- (a) {}^1\Sigma_g^+
- (b) {}^1\Sigma_u^+
- (c) {}^3\Sigma_g^-
- (d) {}^3\Sigma_u^+
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Answer: (d)
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Q48 · 2016 · 2 marks
Complex [\mathrm{Cr}(\mathrm{bipyridyl})_3]^{+3}, shows red phosphorescence due to transition [CSIR-JUNE 2016]
- (a) ^{4}\mathrm{T}_{2\mathrm{g}} \leftarrow {}^{4}\mathrm{A}_{2\mathrm{g}}
- (b) ^{4}\mathrm{T}_{1\mathrm{g}} \leftarrow {}^{4}\mathrm{A}_{2\mathrm{g}}
- (c) ^{4}\mathrm{A}_{2\mathrm{g}} \leftarrow {}^{2}\mathrm{E}_{\mathrm{g}}
- (d) ^{2}\mathrm{E}_{\mathrm{g}} \leftarrow {}^{4}\mathrm{A}_{2\mathrm{g}}
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Answer: (c)
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Q49 · 2016 · 2 marks
Paramagnetic susceptibility of the order of 10^{-6}\ \mathrm{cm^3\,mol^{-1}} observed for \mathrm{KMnO_4} is due to- [CSIR-JUNE 2016]
- (a) random spin alignment
- (c) paramagnetic impurity
- (b) antiferromagnetic exchange interaction
- (d) temperature independent paramagnetism
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Answer: (d)
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Q50 · 2016 · 2 marks
The nephelauxetic parameter \beta is highest for [CSIR-DEC 2016]
- (a) \mathrm{Br}^{-}
- (b) \mathrm{Cl}^{-}
- (c) \mathrm{CN}^{-}
- (d) \mathrm{F}^{-}
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Answer: (d)
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Q51 · 2016 · 2 marks
The {}^{2}\mathrm{E}_{g} \leftarrow {}^{4}\mathrm{A}_{2g} transition in the electronic spectrum of \mathrm{[Cr(NH_3)_6]^{+3}} occurs nearly at [CSIR-DEC 2016]
- (a) 650 nm
- (b) 450 nm
- (c) 350 nm
- (d) 200 nm
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Answer: (a)
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Q52 · 2016 · 2 marks
The correct statement for a Fischer carbene complex is [CSIR-DEC 2016]
- (a) the carbene carbon is electrophilic in nature
- (b) metal exists in high oxidation state
- (c) metal fragment and carbene are in the triplet states
- (d) CO ligands destabilize the complex
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Answer: (a)
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Q53 · 2016 · 2 marks
The highest molecular orbitals for an excited electronic configuration of the oxygen molecule are [1\pi_g]^1\,[3\sigma_u]^1. A possible molecular term symbol for oxygen with this electronic configuration is [CSIR-DEC 2016]
- (a) {}^{1}\pi
- (b) {}^{3}\Sigma
- (c) {}^{1}\Delta
- (d) {}^{1}\Sigma
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Answer: (a)
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Q54 · 2016 · 2 marks
The relative rates of water exchange for the hydrated complexes of (1) \mathrm{Ni}^{+2} (2) \mathrm{V}^{+2} and (3) \mathrm{Cr}^{3+} ions follows the trend: [CSIR-JUNE 2017]
- (a) (1) > (2) > (3)
- (b) (1) < (2) < (3)
- (c) (1) > (2) < (3)
- (d) (1) < (2) > (3)
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Answer: (a)
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Q55 · June 2016 · 2 marks
The number of microstates present in { }^{3} \mathrm{~F}-term is
- (a) 3
- (b) 21
- (c) 9
- (d) 28
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Answer: (b)
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Q56 · 2016 · 2 marks
Chelate effect is [CSIR-JUNE 2016]
- (a) predominantly due to enthalpy change
- (b) predominantly due to entropy change
- (c) independent of ring size
- (d) due to equal contribution of entropy and enthalpy change
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Answer: (b)
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Q57 · June 2016 · 2 marks
The lowest energy term for the \mathrm{d}^{6} configuration is
- (a) { }^{2} \mathrm{D}
- (b) { }^{5} \mathrm{D}
- (c) { }^{1} \mathrm{P}
- (d) { }^{1} \mathrm{D}
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Answer: (b)
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Q58 · June 2016 · 2 marks
The first excited state of hydrogen molecule is
- (a) { }^{1} \sum_{\mathrm{g}}^{+}
- (b) { }^{1} \sum_{u}^{+}
- (c) { }^{3} \sum_{\mathrm{g}}^{-}
- (d) { }^{3} \sum_{u}^{+}
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Answer: (d)
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Q59 · June 2016 · 2 marks
Complex \left[\mathrm{Cr}(\text { bipyridyl })_{3}\right]^{+3}, shows red phosphorescence due to transition
- (a) { }^{4} \mathrm{~T}_{2 \mathrm{~g}} \leftarrow{ }^{4} \mathrm{~A}_{2 \mathrm{~g}}
- (b) { }^{4} \mathrm{~T}_{1 \mathrm{~g}} \leftarrow{ }^{4} \mathrm{~A}_{2 \mathrm{~g}}
- (c) { }^{4} \mathrm{~A}_{2 \mathrm{~g}} \leftarrow{ }^{2} \mathrm{Eg}
- (d) { }^{2} \mathrm{Eg} \leftarrow{ }^{4} \mathrm{~A} 2 \mathrm{~g}
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Answer: (c)
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Q60 · 2016 · 2 marks
The complex that shows orbital contribution to the magnetic moment, is
- (a) \left[\mathrm{Cu}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{+2}
- (b) \left[\mathrm{Ni}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{+2}
- (c) \left[\mathrm{Co}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{+2}
- (d) \left[\mathrm{Cr}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{+2}
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Answer: (c)
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Q61 · 2016 · 2 marks
The room temperature magnetic moment ( in BM) for a monomeric Cu(II) complex is greater than 1.73 . This may be explained using the expression: [CSIR-JUNE 2016]
- (a) \boldsymbol{\mu}_{\text {eff }}=\boldsymbol{\mu}_{\mathrm{s}}\left(\mathbf{1}-\frac{\lambda \alpha}{\Delta}\right)
- (b) \mu_{\text {eff }}=\sqrt{n(n+2)}
- (c) \mu_{\text {eff }}=\sqrt{4 s(s+1)+L(L+1)}
- (d) \mu_{\mathrm{eff}}=\mathrm{g} \sqrt{J(J+1)}
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Answer: (a)
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Q62 · 2016 · 2 marks
The HOMO (highest occupied molecular orbital) to LUMO (lowest unoccupied molecular orbital) electronic transition responsible for the observed colours of halogen molecules (gas) is
- (a) \pi^{*} \rightarrow \sigma^{*} \mathrm{NO}_{2}^{-}
- (b) \pi^{*} \rightarrow \pi^{*} \mathrm{NCS}^{-}
- (c) \sigma \rightarrow \sigma^{*} \mathrm{Cl}^{-}
- (d) \pi \rightarrow \sigma^{*} 13 product is the least, when A is \mathrm{OH}^{-}
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Answer: (a)
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Q63 · 2016 · 2 marks
In the hydrolysis of trans-[\mathrm{Co}(\mathrm{en})_{2}\mathrm{Cl}(\mathrm{A})]^{+} if the leaving group is chloride, the formation of cis product is the least, when A is
- (a) \mathrm{NO}_{2}^{-}
- (b) \mathrm{NCS}^{-}
- (c) \mathrm{Cl}^{-}
- (d) \mathrm{OH}^{-}
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Answer: (a)
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Q64 · Dec 2016 · 2 marks
The nephelauxetic parameter \beta is highest for
- (a) \mathrm{Br}^{-}
- (b) \mathrm{Cl}^{-}
- (c) \mathrm{CN}^{-}
- (d) \mathrm{F}^{-}
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Answer: (d)
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Q65 · Dec 2016 · 2 marks
The { }^{2} \mathrm{Eg}_{\mathrm{g}} \leftarrow^{4} \mathrm{~A}_{2 \mathrm{~g}} transition in the electronic spectrum of \left[\mathrm{Cr}\left(\mathrm{NH}_{3}\right)_{6}\right]^{+3} occurs nearly at
- (a) 650 nm
- (b) 450 nm
- (c) 350 nm
- (d) 200 nm
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Answer: (a)
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Q66 · 2016 · 2 marks
For \left[\mathrm{Ce}\left(\mathrm{NO}_{3}\right)_{4}\left(\mathrm{OPPh}_{3}\right)_{2}\right] from the following
- (a) Its aqueous solution yellow-orange in
- (b) Coordination number of Ce is ten
- (c) It shows metal to ligand charge transfer
- (d) It is diamagnetic in nature
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Answer: (c)
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Q67 · 2016 · 2 marks
Consider the following statements for \left[\mathrm{FeO}_{4}\right]^{-4}
- (a) It is paramagnetic
- (b) It has \mathrm{T}_{\mathrm{d}} symmetry
- (c) Adopts distorted square planar geometry
- (d) Shows approximately \mathrm{D}_{2 \mathrm{~d}} symmetry
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Answer: (c)
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Q68 · 2016 · 2 marks
The spectroscopic ground state term symbols for the octahedral aqua complexes of \mathrm{Mn}(\mathrm{II}), Cr(III) and Cu(II), respectively, are
- (a) { }^{2} \mathrm{H},{ }^{4} \mathrm{~F} and { }^{2} \mathrm{D}
- (b) { }^{6} \mathrm{~S},{ }^{4} \mathrm{~F} and { }^{2} \mathrm{D}
- (c) { }^{2} \mathrm{H},{ }^{2} \mathrm{H} and { }^{2} \mathrm{D}
- (d) { }^{6} \mathrm{~S},{ }^{4} \mathrm{~F} and { }^{2} \mathrm{P}
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Answer: (b)
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Q69 · 2016 · 2 marks
In the following redox reaction with an equilibrium constant \mathrm{K}=2.0 \times 10^{8} \left[\mathrm{Ru}\left(\mathrm{NH}_{3}\right)_{6}\right]^{+2}+\left[\mathrm{Fe}\left(\mathrm{H}_{2} \mathrm{O}_{6}\right)\right]^{+3} \rightarrow\left[\mathrm{Ru}\left(\mathrm{NH}_{3}\right)_{6}\right]^{+3}+\left[\mathrm{Fe}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{+2} the self exchange rates for oxidant and reductant are 5.0 \mathrm{M}^{-1} \mathrm{~s}^{-1} and 4.0 \times 10^{3} \mathrm{M}^{-1} \mathrm{~s}^{-1} respectively. The approximate rate constant \left(\mathrm{M}^{-1} \mathrm{~s}^{-1}\right) for the reaction is
- (a) 3.16 \times 10^{6}
- (b) 2.0 \times 10^{6}
- (c) 6.32 \times 10^{6}
- (d) 3.16 \times 10^{6}
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Answer: (b)
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Q70 · Dec 2016 · 2 marks
The correct statement for a Fischer carbene complex is
- (a) the carbene carbon is electrophilic in nature
- (b) metal exists in high oxidation state
- (c) metal fragment and carbene are in the triplet states
- (d) CO ligands destabilize the complex 14
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Answer: (a)
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Q71 · Dec 2016 · 2 marks
The highest molecular orbitals for an excited electronic configuration of the oxygen molecule are [1 \pi \mathrm{~g}]^{1}[3 \sigma \mathrm{u}]^{1}. A possible molecular term symbol for oxygen with this electronic configuration is
- (a) { }^{1} \pi
- (b) { }^{3} \Sigma
- (c) { }^{1} \Delta
- (d) { }^{1} \Sigma
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Answer: (a)
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Q72 · 2015 · 2 marks
The formation constant for the complexation of \mathrm{M}^{+} (M = Li, Na, K and Cs) with cryptand, C222 follows the order [CSIR-DEC 2015]
- (a) \mathrm{Li^+ < Cs^+ < Na^+ < K^+}
- (b) \mathrm{Li^+ < Na^+ < K^+ < Cs^+}
- (c) \mathrm{K^+ < Cs^+ < Li^+ < Na^+}
- (d) \mathrm{Cs^+ < K^+ < Li^+ < Na^+}
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Answer: (a)
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Q73 · June 2015 · 2 marks
In transition metal phosphine \left(\mathrm{M}-\mathrm{PR}_{3}\right) complexes, the back-bonding involves donation of electrons from
- (a) \mathrm{M}\left(\mathrm{t}_{2 \mathrm{~g}}\right) \rightarrow \mathrm{PR}_{3}\left(\sigma^{*}\right)
- (b) \mathrm{M}\left(\mathrm{t}_{2 \mathrm{~g}}\right) \rightarrow \mathrm{PR}_{3}\left(\pi^{*}\right)
- (c) \mathrm{M}\left(\mathrm{e}_{\mathrm{g}}\right) \rightarrow \mathrm{P}(\mathrm{d})
- (d) \mathrm{PR}_{3}(\pi) \rightarrow \mathrm{M}\left(\mathrm{t}_{2 \mathrm{~g}}\right)
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Answer: (a)
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Q74 · 2015 · 2 marks
Among the complexes, (\mathrm{A}) \mathrm{K}_{4}\left[\mathrm{Cr}(\mathrm{CN})_{6}\right], \mathrm{K}_{4}\left[\mathrm{Fe}(\mathrm{CN})_{6}\right], (\mathrm{C}) \mathrm{K}_{3}\left[\mathrm{Co}(\mathrm{CN})_{6}\right], (\mathrm{D}) \mathrm{K}_{4}\left[\mathrm{Mn}(\mathrm{CN})_{6}\right], and \mathrm{Jahn}- Teller distortion is expected in
- (a) A, B and C
- (b) B, C and D
- (c) A and D
- (d) B and C
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Answer: (c)
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Q75 · June 2015 · 2 marks
The complex \left[\mathrm{Fe}(\text { phen })_{2}(\mathrm{NCS})_{2}\right] (phen 1,10-phenanthroline) shows spin cross-over behaviour CFSE and at \mu_{\text {eff }} 250 and 150 K , respectively are
- (a) 0.4 \Delta_{0}, 4.90 \mathrm{BM} and 2.4 \Delta, 0.00 \mathrm{BM}
- (b) 2.4 \Delta_{0}, 2.90 \mathrm{BM} and 0.4 \Delta, 1.77 \mathrm{BM}
- (c) 2.4 \Delta_{0}, 0.00 \mathrm{BM} and 0.4 \Delta, 4.90 \mathrm{BM}
- (d) 1.2 \Delta_{0}, 4.90 \mathrm{BM} and 2.4 \Delta .0 .00 \mathrm{BM}
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Answer: (a)
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Q76 · 2015 · 2 marks
The oxidizing power of \left[\mathrm{CrO}_{4}\right]^{2-},\left[\mathrm{MnO}_{4}\right]^{2-} and \left[\mathrm{FeO}_{4}\right]^{2-} follows the order
- (a) \left[\mathrm{CrO}_{4}\right]^{2-}<\left[\mathrm{MnO}_{4}\right]^{2-}<\left[\mathrm{FeO}_{4}\right]^{2-}
- (b) \left[\mathrm{FeO}_{4}\right]^{2-}<\left[\mathrm{MnO}_{4}\right]^{2-}<\left[\mathrm{CrO}_{4}\right]^{2-}
- (c) \left[\mathrm{MnO}_{4}\right]^{2-}<\left[\mathrm{FeO}_{4}\right]^{2-}<\left[\mathrm{CrO}_{4}\right]^{2-}
- (d) \left[\mathrm{CrO}_{4}\right]^{2-}<\left[\mathrm{FeO}_{4}\right]^{2-}<\left[\mathrm{MnO}_{4}\right]^{2-}
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Answer: (a)
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Q77 · 2015 · 2 marks
Using crystal field theory, identify from the following complex ions that shows same \mu_{\text {eff }} (spin only) values
- (a) \left[\mathrm{CoF}_{6}\right]^{3-} A and B
- (b) \left[\mathrm{IrCl}_{6}\right]^{3-} B and C
- (c) \left[\mathrm{Fe}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{2+} [CSIR-DEC 2015] A and C
- (d) A, B and C
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Answer: (c)
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Q78 · 2015 · 2 marks
The correct statement for \mathrm{Mn}-\mathrm{O} bond lengths in \left[\mathrm{Mn}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{2+}, is [CSIR-DEC 2015]
- (a) all bonds are equal
- (b) four bonds are longer than two others
- (c) two bonds are longer than four others
- (d) they are shorter than the \mathrm{Mn}-\mathrm{O} bond in \left[\mathrm{MnO}_{4}\right]^{-}
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Answer: (a)
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Q79 · 2015 · 2 marks
Identify the complex ions in sequential order when ferroin is used as an indicator in the titration of iron(II) with potassium dichromate, (phen = 1, 10-phenathroline)
- (a) \left[\mathrm{Fe}(\text { phen })_{3}\right]^{2+} and \left[\mathrm{Fe}(\text { phen })_{3}\right]^{3+}
- (b) \left[\mathrm{Fe}(\mathrm{phen})_{3}\right]^{3+} and \left[\mathrm{Fe}(\mathrm{phen})_{3}\right]^{2+}
- (c) \left[\mathrm{Fe}(\mathrm{CN})_{6}\right]^{4-} and \left[\mathrm{Fe}(\mathrm{CN})_{6}\right]^{3-}
- (d) \left[\mathrm{Fe}(\mathrm{CN})_{6}\right]^{3-} and \left[\mathrm{Fe}(\mathrm{CN})_{6}\right]^{4-}
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Answer: (a)
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Q80 · 2015 · 2 marks
The correct statement about the substitution reaction of \left[\mathrm{Co}(\mathrm{CN}){ }_{5} \mathrm{Cl}\right]^{3-} with OH - to give \left[\mathrm{Co}(\mathrm{CN})_{5}(\mathrm{OH})\right]^{3-} is,
- (a) it obeys first order kinetics
- (b) its rate is proportional to the concentration of both the reactants
- (c) it follows the \mathrm{SN}^{1}{ }_{\mathrm{CB}} mechanism
- (d) its rate is dependent only on the concentration of [\mathrm{OH}]^{-}
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Answer: (a)
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Q81 · 2015 · 2 marks
Aqueous \mathrm{Cr}^{+2} effects one electron reduction of \left[\mathrm{Co}\left(\mathrm{NH}_{3}\right)_{5} \mathrm{Cl}\right]^{+2} giving compound Y . Compound Y undergoes rapid hydrolysis. Y is,
- (a) \left[\mathrm{Co}\left(\mathrm{NH}_{3}\right)_{5}\right]^{+2}
- (b) \left[\mathrm{Co}\left(\mathrm{NH}_{3}\right)_{5}(\mathrm{OH})\right]^{+}
- (c) \left[\mathrm{Co}\left(\mathrm{NH}_{3}\right)_{4}(\mathrm{OH})_{2}\right]
- (d) \left[\mathrm{Cr}\left(\mathrm{H}_{2} \mathrm{O}\right)_{5} \mathrm{Cl}\right]^{+2}
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Answer: (a)
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Q82 · 2015 · 2 marks
Three electronic transitions at 14900,22700 and 34400 \mathrm{~cm}^{-1} are observed in the absorption spectrum of \left[\mathrm{CrF}_{6}\right]^{-3}, The \Delta 0 value (in \mathrm{cm}^{-1} ) and the corresponding transition are
- (a) 7800 and { }^{4} \mathrm{~A}_{2 \mathrm{~g}} \rightarrow{ }^{4} \mathrm{~T}_{2} \mathrm{~g}
- (b) 14900 and { }^{4} \mathrm{~A}_{2 \mathrm{~g}} \rightarrow{ }^{4} \mathrm{~T}_{2} \mathrm{~g}
- (c) 14900 and { }^{4} \mathrm{~T}_{1} \mathrm{~g} \rightarrow{ }^{4} \mathrm{~T}_{1} \mathrm{~g}(\mathrm{~F})
- (d) 7800 and { }^{4} \mathrm{~T}_{2 \mathrm{~g}} \rightarrow{ }^{3} \mathrm{~T}_{1 \mathrm{~g}}(\mathrm{~F})
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Answer: (b)
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Q83 · 2014 · 2 marks
Reaction of nitrosyl tetrafluoroborate to Vaska's complex gives complex A with angle \mathrm{M-N-O}=124^{\circ}. The complex A and its \mathrm{N-O} stretching frequency are, respectively [CSIR-JUNE 2014]
- (a) [\mathrm{IrCl(CO)(NO)(PPh_3)_2}]\mathrm{BF_4},\ 1620\ \mathrm{cm}^{-1}
- (b) [\mathrm{IrCl(CO)(NO)_2(PPh_3)}](\mathrm{BF_4})_2,\ 1730\ \mathrm{cm}^{-1}
- (c) [\mathrm{IrCl(CO)(NO)_2(PPh_3)}](\mathrm{BF_4})_2\ 1520\ \mathrm{cm}^{-1}
- (d) [\mathrm{IrCl(CO)(NO)(PPh_3)_2}],\ 1820\ \mathrm{cm}^{-1}
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Answer: (a)
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Q84 · 2014 · 2 marks
An aqueous solution of \mathrm{[Mn(H_2O)_6]^{+2}} complex is pale pink in colour. The probable reasons for it are [CSIR-DEC 2014] (A) Presence of {}^{6}\mathrm{A_{1}g} ground state (B) Disallowed transition by spin selection rule (C) Presence of {}^{2}\mathrm{T_{2}g} ground state (D) Charge transfer transition. The correct answer is
- (a) A and B
- (b) A and C
- (c) B and C
- (d) C and D
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Answer: (a)
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Q85 · 2014 · 2 marks
In transition metal phosphine (\mathrm{M{-}PR_3}) complexes, the back-bonding involves donation of electrons from [CSIR-JUNE 2015]
- (a) \mathrm{M}(t_{2g}) \rightarrow \mathrm{PR_3}(\sigma^*)
- (b) \mathrm{M}(t_{2g}) \rightarrow \mathrm{PR_3}(\pi^*)
- (c) \mathrm{M}(e_g) \rightarrow \mathrm{P}(d)
- (d) \mathrm{PR_3}(\pi) \rightarrow \mathrm{M}(t_{2g})
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Answer: (a)
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Q86 · 2013 · 2 marks
In bis(dimethylglyoximato)nickel(II), the number of Ni-N, Ni-O and intramolecular hydrogen bond(s)respectively are [CSIR-JUNE 2014]
- (a) 4,0 and 2
- (b) 2, 2 and 2
- (c) 2, 2 and 0
- (d) 4, 0 and 1
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Answer: (a)
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Q87 · 2014 · 2 marks
\mathrm{NiBr}_{2} reacts with (\mathrm{Et})\left(\mathrm{Ph}_{2}\right) \mathrm{P} at -78^{\circ} \mathrm{C} in \mathrm{CS}_{2} to give red compound ' A ', which upon standing at room temperature turns green to give compound, 'B' of the same formula. The measured magnetic moments of ' A ' and ' B ' are 0.0 and 3.2 BM, respectively. The geometries of ' A ' and ' B ' are
- (a) square planar and tetrahedral
- (b) tetrahedral and square planar
- (c) square planar and octahedral
- (d) tetrahedral and octahedral
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Answer: (a)
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Q88 · 2014 · 2 marks
If L is a neutral mono-dentate ligand, the species, \left[\mathrm{AgL}_{4}\right]^{2+},\left[\mathrm{AgL}_{6}\right]^{2+} and \left[\mathrm{AgL}_{4}\right]^{3+} respectively are
- (a) Paramagnetic, paramagnetic and diamagnetic
- (b) Paramagnetic, diamagnetic and paramagnetic
- (c) Diamagnetic, paramagnetic and diamagnetic
- (d) Paramagnetic, diamagnetic and diamagnetic
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Answer: (a)
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Q89 · 2014 · 2 marks
\left[\mathrm{CoL}_{6}\right]^{3+} is red in colour whereas \left[\mathrm{CoL}_{6}^{\prime}\right]^{3+} is green. L. and \mathrm{L}^{\prime} respectively corresponds to,
- (a) \mathrm{NH}_{3} and \mathrm{H}_{2} \mathrm{O}
- (b) \mathrm{NH}_{3} and 1, 10-phenanthroline
- (c) \mathrm{H}_{2} \mathrm{O} and 1, 10-phenanthroline
- (d) \mathrm{H}_{2} \mathrm{O} and \mathrm{NH}_{3}
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Answer: (a)
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Q90 · 2014 · 2 marks
The term symbol that is NOT allowed for the n p^{2} configuration is
- (a) { }^{1} \mathrm{D}
- (b) { }^{3} \mathrm{P}
- (c) { }^{1} \mathrm{~S}
- (d) { }^{3} \mathrm{D}
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Answer: (d)
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Q91 · 2014 · 2 marks
Identify the correct statement about \left[\mathrm{Ni}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{+2} and \left[\mathrm{Cu}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{+2} [CSIR-JUNE 2014]
- (a) All Ni-O and Cu-O bond lengths of individual species are equal
- (b) Ni-O(equatorial) and Cu-O(equatorial)
- (c) All Ni-O bond lengths are equal whereas Cu-O (equatorial) bonds are shorter than Cu O(axial) bonds
- (d) All Cu-O bond lengths are equal whereas Ni-O(equatorial) bonds are shorter than Ni O(axial)bonds
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Answer: (c)
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Q92 · June 2014 · 2 marks
Reaction of nitrosyltetrafluoroborate to Vaska's complex gives complex A with angle \mathrm{M}-\mathrm{NO}=124^{\circ}. The complex A and its N-O stretching frequency are, respectively
- (a) \left[\mathrm{IrCl}(\mathrm{CO})(\mathrm{NO})\left(\mathrm{PPh}_{3}\right)_{2}\right] \mathrm{BF}_{4}, 1620 \mathrm{~cm}^{-1}
- (b) \left[\operatorname{IrCl}(\mathrm{CO})(\mathrm{NO})_{2}\left(\mathrm{PPh}_{3}\right)\right]\left(\mathrm{BF}_{4}\right)_{2}, 1730 \mathrm{~cm}^{-1}
- (c) \left[\mathrm{IrCl}(\mathrm{CO})(\mathrm{NO})_{2}\left(\mathrm{PPh}_{3}\right)\right]\left(\mathrm{BF}_{4}\right)_{2} 1520 \mathrm{~cm}^{-1}
- (d) \left[\operatorname{IrCl}(\mathrm{CO})(\mathrm{NO})\left(\mathrm{PPh}_{3}\right)_{2}\right], 1820 \mathrm{~cm}^{-1}
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Answer: (a)
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Q93 · 2014 · 2 marks
The S and L values for { }^{15} \mathrm{~N} atom respectively, are
- (a) 1/2 and 1
- (b) 1/2 and 0
- (c) 1 and 0
- (d) 3 / 2 and 0
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Answer: (d)
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Q94 · 2014 · 2 marks
In the following reaction \left[\mathrm{PtCl}_{4}\right]^{-2}+\mathrm{NO}_{2}^{-}, is \rightarrow \mathrm{A}+\mathrm{NH}_{3} \rightarrow \mathrm{~B}, compound B is [CSIR-DEC 2014]
- (a) trans- \left[\mathrm{PtCl}_{2}\left(\mathrm{NO}_{2}\right)\left(\mathrm{NH}_{3}\right)\right]^{-}
- (b) cis- \left[\mathrm{PtCl}\left(\mathrm{NO}_{2}\right)\left(\mathrm{NH}_{3}\right)\right]^{-}
- (c) trans- \left[\mathrm{PtCl}_{2}\left(\mathrm{NH}_{3}\right)_{2}\right]
- (d) cis- \left[\mathrm{PtCl}_{3}\left(\mathrm{NO}_{2}\right)_{2}\right]^{-2}
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Answer: (a)
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Q95 · Dec 2014 · 2 marks
An aqueous solution of \left[\mathrm{Mn}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{+2} complex is pale pink in colour. The probable reasons for it are
- (a) Presence of { }^{6} \mathrm{~A}_{1 \mathrm{~g}} ground state
- (b) Disallowed transition by spin selection rule
- (c) Presence of { }^{2} \mathrm{~T}_{2 \mathrm{~g}} ground state
- (d) Charge transfer transition
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Answer: (a)
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Q96 · Dec 2014 · 2 marks
Base hydrolysis of \left[\mathrm{CoCl}\left(\mathrm{NH}_{3}\right)_{5}\right]^{+2} is an overall second order reaction, whereas that of [\mathrm{Co}(\mathrm{CN})]^{-3} is of first order. The rates depend in both cases solely on the concentrations of the cobalt complex. This may be due to
- (a) Presence of ionizable proton in \left[\mathrm{CoCl}\left(\mathrm{NH}_{3}\right)_{5}\right]^{+2} but not in \left[\mathrm{Co}(\mathrm{CN})_{6}\right]^{-3}, A and B
- (b) \mathrm{SN}^{1}{ }_{\mathrm{CB}} mechanism in the case of \left[\mathrm{CoCl}\left(\mathrm{NH}_{3}\right)_{5}\right]^{+2} only A and C
- (c) \mathrm{SN}^{1}{ }_{\mathrm{CB}} mechanism in the case of \left[\mathrm{Co}(\mathrm{CN})_{6}\right]^{-3}, only B only
- (d) \mathrm{SN}^{1}{ }_{\mathrm{CB}} mechanism in both the complexes Correct explanation(s) is/are A and D
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Answer: (a)
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Q97 · 2014 · 2 marks
The configuration [\mathrm{Ne}] 2 p^{1} 3 p^{1} has a { }^{3} \mathrm{D} term. Its levels are
- (a) { }^{3} \mathrm{D}_{3 / 2},{ }^{3} \mathrm{D}_{1 / 2}
- (b) { }^{3} \mathrm{D}_{5 / 2},{ }^{3} \mathrm{D}_{3 / 2},{ }^{3} \mathrm{D}_{1 / 2}
- (c) { }^{3} \mathrm{D}_{3},{ }^{3} \mathrm{D}_{2},{ }^{3} \mathrm{D}_{1}
- (d) { }^{3} \mathrm{D}_{3},{ }^{3} \mathrm{D}_{2},{ }^{3} \mathrm{D}_{1},{ }^{3} \mathrm{D}_{0}
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Answer: (c)
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Q98 · 2014 · 2 marks
The spin-only magnetic moment and the spectroscopic ground state term symbol of manganese center in \left[\mathrm{MnF}_{6}\right]^{-3} ion respectively, are
- (a) 4.9 BM and { }^{5} \mathrm{D}
- (b) 4.9 BM and { }^{4} \mathrm{~F}
- (c) 3.9 BM and { }^{3} \mathrm{D}
- (d) 4.9 BM and { }^{3} \mathrm{~F}
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Answer: (a)
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Q99 · 2014 · 2 marks
The three dimensional structure of compound \left[\mathrm{Co}\left(\mathrm{Co}\left(\mathrm{NH}_{3}\right)_{4}(\mathrm{OH})_{2}\right)_{3}\right] \mathrm{Br}_{6}, has [CSIR-DEC 2014]
- (a) Twelve \mathrm{Co}-\mathrm{O} and twelve \mathrm{Co}-\mathrm{N} bonds
- (b) Ten Co-O and ten Co-N bonds
- (c) Fourteen Co-O and ten Co-N bonds
- (d) Twelve Co-O and ten Co-N bonds
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Answer: (a)
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Q100 · 2014 · 2 marks
The spin-only and spin plus orbital magnetic moments of \left[\mathrm{CrCl}_{6}\right]^{-3} are [CSIR-DEC 2014]
- (a) 3.87 BM and 5.20 BM
- (b) 2.84 BM and 5.20 BM
- (c) 3.87 BM and 6.34 BM
- (d) 2.84 BM and 6.34 BM
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Answer: (a)
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Q101 · 2013 · 2 marks
The species with highest magnetic moment (spin only value) is [CSIR-JUNE 2013]
- (a) \mathrm{VCl_6^{4-}}
- (b) (\eta^5\text{-}\mathrm{C_5H_5})_2\mathrm{Cr}
- (c) \mathrm{[Co(NO_2)_6]^{3-}}
- (d) \mathrm{[Ni(EDTA)]^{2-}}
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Answer: (a)
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Q102 · 2013 · 2 marks
An octahedral metal ion \mathrm{M^{+2}} has magnetic moment of 4.0 B.M. The correct combination of metal ion and d-electron configuration is given by [CSIR-DEC 2013]
- (a) \mathrm{Co^{2+}},\ t_{2g}^{5}e_{g}^{2}
- (b) \mathrm{Cr^{2+}},\ t_{2g}^{4}e_{g}^{2}
- (c) \mathrm{Mn^{2+}},\ t_{2g}^{3}e_{g}^{1}
- (d) \mathrm{Fe^{2+}},\ t_{2g}^{4}e_{g}^{2}
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Answer: (a)
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Q103 · 2013 · 2 marks
\mathrm{MnCr_2O_4} is likely to have a normal spinel structure because [CSIR-DEC 2013]
- (a) \mathrm{Mn^{2+}} will have a LFSE in the octahedral site whereas the Cr will not
- (b) Mn is +2 oxidation state and both the Cr are in +3 oxidation state.
- (c) Mn is +3 oxidation state and 1 Cr is in +2 and the other is in +3 state.
- (d) \mathrm{Cr^{3+}} will have a LFSE in the octahedral site whereas the \mathrm{Mn^{2+}} ion will not.
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Answer: (d)
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Q104 · 2013 · 2 marks
Compounds \mathrm{K_2Ba[Cu(NO_2)_6]} (A) and \mathrm{Cs_2Ba[Cu(NO_2)_6]} (B) exhibit tetragonal elongation and tetragonal compression, respectively. The unpaired electron in A and B are found respectively, in orbitals [CSIR-DEC 2013]
- (a) d_{z^2} and d_{x^2-y^2},
- (b) d_{x^2-y^2} and d_{z^2}
- (c) d_{z^2} and d_{z^2}
- (d) d_{x^2-y^2} and d_{x^2-y^2}
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Answer: (b)
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Q105 · 2012 · 2 marks
The reaction of \mathrm{Pt}\left(\mathrm{NH}_{3}\right)_{4}{ }^{2-} with two equivalents of \mathrm{NH}_{3} produces
- (a) cis- \left[\mathrm{Pt}\left(\mathrm{NH}_{3}\right)_{2} \mathrm{Cl}_{2}\right]
- (b) trans -\left[\mathrm{Pt}\left(\mathrm{NH}_{3}\right)_{2} \mathrm{Cl}_{2}\right]
- (c) both cis- \left[\mathrm{Pt}\left(\mathrm{NH}_{3}\right)_{2} \mathrm{Cl}_{2}\right] and trans -\left[\mathrm{Pt}\left(\mathrm{NH}_{3}\right)_{2} \mathrm{Cl}_{2}\right]
- (d) cis -\left[\mathrm{Pt}\left(\mathrm{NH}_{3}\right)_{2} \mathrm{Cl}_{4}\right]^{2-}
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Answer: (a)
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Q106 · 2013 · 2 marks
The electronic transition responsible for the colour of the transition metal ions is
- (a) \mathrm{d}_{\pi} \rightarrow \mathrm{d}_{\sigma}
- (b) \mathrm{d}_{\pi} \rightarrow \mathrm{d}_{\sigma} *
- (c) \mathrm{d}_{\pi} \rightarrow \mathrm{d}_{\pi}{ }^{*}
- (d) \mathrm{d}_{\sigma} \rightarrow \mathrm{d}_{\pi}{ }^{*}
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Answer: (b)
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Q107 · 2013 · 2 marks
The Mulliken symbols for the spectroscopic states arising from the free-ion term F are
- (a) \mathrm{T}_{2 \mathrm{~g}}+\mathrm{E}_{\mathrm{g}}
- (b) \mathrm{T}_{1 \mathrm{~g}}+\mathrm{T}_{2 \mathrm{~g}}+\mathrm{T}_{1 \mathrm{u}}
- (c) \mathrm{T}_{1 \mathrm{~g}}+\mathrm{T}_{2 \mathrm{~g}}+\mathrm{A}_{2 \mathrm{~g}}(\mathrm{~d}) \mathrm{A}_{1 \mathrm{~g}}+\mathrm{T}_{2 \mathrm{~g}}+\mathrm{T}_{1 \mathrm{~g}}
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Answer: (c)
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Q108 · 2013 · 2 marks
Intense band at 15000 cm-1 in the UV-visible spectrum of \left[\mathrm{Bu}_{4} \mathrm{~N}\right]_{2} \mathrm{Re}_{2} \mathrm{Cl}_{8} is due to the transition [CSIR-JUNE 2013]
- (a) \pi \rightarrow \pi^{*}
- (b) \boldsymbol{\delta} \rightarrow \boldsymbol{\delta}^{*}
- (c) \boldsymbol{\delta} \rightarrow \boldsymbol{\pi}^{*}
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Answer: (b)
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Q109 · 2013 · 2 marks
Identify the order representing increasing \pi-acidity of the following ligands \mathrm{C}_2\mathrm{F}_4, \mathrm{NEt}_3, \mathrm{CO} and \mathrm{C}_2\mathrm{H}_4
- (a) \mathrm{CO}<\mathrm{C}_2\mathrm{F}_4<\mathrm{C}_2\mathrm{H}_4<\mathrm{NEt}_3
- (b) \mathrm{C}_2\mathrm{F}_4<\mathrm{C}_2\mathrm{H}_4<\mathrm{NEt}_3<\mathrm{CO}
- (c) \mathrm{C}_2\mathrm{H}_4<\mathrm{NEt}_3<\mathrm{CO}<\mathrm{C}_2\mathrm{F}_4
- (d) \mathrm{NEt}_3<\mathrm{C}_2\mathrm{H}_4<\mathrm{C}_2\mathrm{F}_4<\mathrm{CO}
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Answer: (d)
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Q110 · June 2013 · 2 marks
The species with highest magnetic moment (spin only value) is
- (a) \mathrm{VCI}_{6}{ }^{4-}
- (b) \left(\eta^{5} \mathrm{C}_{5} \mathrm{H}_{5}\right)_{2} \mathrm{Cr}
- (c) \left[\mathrm{Co}\left(\mathrm{NO}_{2}\right)_{6}\right]^{3-}
- (d) [Ni(EDTA)] { }^{2-}
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Answer: (a)
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Q111 · Dec 2013 · 2 marks
An octahedral metal ion \mathrm{M}^{+2} has magnetic moment of 4.0 B.M. The correct combination of metal ion and d-electron configuration is given by
- (a) \mathrm{Co}^{2+},\ t_{2g}^{5}\ e_g^{2}
- (b) \mathrm{Cr}^{2+},\ t_{2g}^{4}\ e_g^{2}
- (c) \mathrm{Mn}^{2+},\ t_{2g}^{3}\ e_g^{1}
- (d) \mathrm{Fe}^{2+},\ t_{2g}^{4}\ e_g^{2}
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Answer: (a)
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Q112 · 2013 · 2 marks
For an electronic configuration of two non-equivalent \pi electronics \left[\pi^{1}, \pi^{1}\right] which of the Following terms is not possible?
- (a) { }^{1} \Sigma
- (b) { }^{3} \Sigma
- (c) { }^{3} \Delta
- (d) { }^{3} \phi
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Answer: (d)
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Q113 · 2013 · 2 marks
Among the following, the correct combination of complex and its color is [CSIR-DEC 2013] Show answer
Answer: (c)
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Q114 · Dec 2013 · 2 marks
\mathrm{MnCr}_{2} \mathrm{O}_{4} is likely to have a normal spinel structure because
- (a) \mathrm{Mn}^{2+} will have a LFSE in the octahedral site whereas the Cr will not
- (b) Mn is { }^{+2} oxidation state and both the Cr are in { }^{+3} oxidation state.
- (c) Mn is { }^{+3} oxidation state and I Cr is \mathrm{in}^{+2} and the other is in { }^{+3} state.
- (d) \mathrm{Cr}^{3+} will have a LFSE in the octahedral site whereas the \mathrm{Mn}^{2+} ion will not.
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Answer: (d)
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Q115 · Dec 2013 · 2 marks
Compounds \mathrm{K}_{2} \mathrm{Ba}\left[\mathrm{Cu}\left(\mathrm{NO}_{2}\right)_{6}\right] (A) and \mathrm{Cs}_{2} \mathrm{Ba}\left[\mathrm{Cu}\left(\mathrm{NO}_{2}\right)_{6}\right] (B) exhibit tetragonal elongation and tetragonal compression, respectively. The unpaired electron in A and B are found respectively, in orbitals
- (a) \mathrm{d}_{\mathrm{z}^{2}} and \mathrm{dx}^{2}-\mathrm{y}^{2},
- (b) \mathrm{dx}^{2}-\mathrm{y}_{2} and \mathrm{d}_{\mathrm{z}^{2}}
- (c) \mathrm{d}_{\mathrm{z}^{2}} and \mathrm{d}_{\mathrm{z}^{2}}
- (d) \mathrm{dx}^{2}-\mathrm{y}^{2} and \mathrm{dx}^{2}-\mathrm{y}^{2}
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Answer: (b)
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Q116 · 2012 · 2 marks
The correct spinel structure of \mathrm{Co}_{3}\mathrm{O}_{4} is: [CSIR-DEC 2012]
- (a) \left(\mathrm{Co}^{+2}\right)_{\mathrm{t}}\left(2\mathrm{CO}^{+3}\right)_{\mathrm{o}}\mathrm{O}_{4}
- (b) \left(\mathrm{Co}^{+2}\right)_{\mathrm{t}}\left(2\mathrm{Co}^{+3}\mathrm{Co}^{+3}\right)_{\mathrm{o}}\mathrm{O}_{4}
- (c) \left(\mathrm{Co}^{+2}\mathrm{Co}^{+3}\right)_{\mathrm{t}}\left(\mathrm{Co}^{+3}\right)_{\mathrm{o}}\mathrm{O}_{4}
- (d) \left(2\mathrm{Co}^{+3}\right)_{\mathrm{t}}\left(\mathrm{Co}^{+2}\right)_{\mathrm{o}}\mathrm{O}_{4}
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Answer: (a)
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Q117 · 2011 · 2 marks
As a ligand Cl - is:
- (a) Only a \sigma-donor
- (b) Only \pi donor
- (c) Both a \sigma-donor and \pi-donor
- (d) A \sigma-donor and a \sigma-acceptor
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Answer: (c)
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Q118 · 2012 · 2 marks
The nucleophilic attack on olefins under mild conditions: [CSIR-JUNE 2012]
- (a) Is always facile
- (b) Is more facile than electrophilic attack on olefins
- (c) Is facile for electron-rich olefins
- (d) Requires activation by coordination to metal.
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Answer: (c)
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Q119 · 2012 · 2 marks
The number of spin-allowed ligand field transitions for octahedral Ni(II) complexes with { }^{3} \mathbf{A}_{\mathbf{2 g}}, ground state is: [CSIR-JUNE 2012]
- (a) Two
- (b) Three
- (c) One
- (d) Four
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Answer: (b)
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Q120 · Dec 2012 · 2 marks
The total number of Cu-O bonds present in the crystalline copper(II) acetate monohydrate is:
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Answer: (a)
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Q121 · 2012 · 2 marks
The electric dipole allowed transition in a \mathrm{d}^{2} atomic system is
- (a) { }^{3} \mathrm{~F} \rightarrow{ }^{1} \mathrm{D}
- (b) { }^{3} \mathrm{~F} \rightarrow{ }^{1} \mathrm{P}
- (c) { }^{3} \mathrm{~F} \rightarrow{ }^{3} \mathrm{D}
- (d) { }^{3} \mathrm{~F} \rightarrow{ }^{3} \mathrm{P}
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Answer: (c)
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Q122 · Dec 2012 · 2 marks
The correct spinel structure of \mathrm{Co}_{3} \mathrm{O}_{4} is:
- (a) \left(\mathrm{Co}^{+2}\right) \mathrm{t}\left(2 \mathrm{CO}^{+3}\right) o \mathrm{O}_{4}
- (b) \left(\mathrm{Co}^{+2}\right) \mathrm{t}\left(2 \mathrm{Co}^{+3} \mathrm{Co}^{+3}\right) o \mathrm{O}_{4}
- (c) \left(\mathrm{Co}^{+2} \mathrm{Co}^{+3}\right) \mathrm{t}\left(\mathrm{Co}^{+3}\right) o \mathrm{O}_{4}
- (d) \left(2 \mathrm{Co}^{+3}\right) \mathrm{t}\left(\mathrm{Co}^{+2}\right) o \mathrm{O}_{4}
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Answer: (a)
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Q123 · 2012 · 2 marks
The platinum complex of \mathbf{N H}_{3} and \mathbf{C l}^{-}ligands is an anti-tumour agent. The correct isomeric formula of the complex and its precursor are: [CSIR-DEC 2012]
- (a) cis- \mathbf{P t}\left(\mathbf{N H}_{\mathbf{3}}\right)_{\mathbf{2}} \mathbf{C l}_{\mathbf{2}} and \mathbf{P t C l}_{\mathbf{4}}{ }^{\mathbf{2 -}}
- (b) trans- \mathrm{Pt}\left(\mathrm{NH}_{3}\right)_{2} \mathrm{Cl}_{2} and \mathrm{PtCl}_{4}{ }^{2-}
- (c) cis- \mathrm{Pt}\left(\mathrm{NH}_{3}\right)_{2} \mathrm{Cl}_{2} and \mathrm{Pt}\left(\mathrm{NH}_{3}\right)_{4}{ }^{2-}
- (d) trans- \mathrm{Pt}\left(\mathrm{NH}_{3}\right)_{2} \mathrm{Cl}_{2} and \mathrm{Pt}\left(\mathrm{NH}_{3}\right)_{4}{ }^{2-}
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Answer: (a)
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Q124 · 2012 · 2 marks
One of the excited states of Ti has the electric configuration [\mathrm{Ar}] 4 \mathrm{~s}^{2} 3 \mathrm{~d}^{1} 4 \mathrm{p}^{1}. The number of microstates with zero total spin (S) for this configuration is
- (a) 9
- (b) 15
- (c) 27
- (d) 60
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Answer: (b)
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Q125 · 2011 · 2 marks
According To Crystal Field Theory, \mathrm{Ni^{2+}} can two have unpaired electrons in [CSIR-JUNE 2011]
- (a) Octahedral geometry only
- (b) Square planar geometry only
- (c) Tetrahedral geometry only
- (d) Both octahedral and tetrahedral geometry
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Answer: (c)
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Q126 · 2011 · 2 marks
The term symbol of a molecule with electronic configuration: (1\sigma_g)^2(1\sigma_u)^2(2\sigma_g)^2(2\sigma_u)^2(1\pi_u)^1(1\pi_u)^1 is: [CSIR-JUNE 2011]
- (a) {}^{1}\Sigma_g^{+}
- (b) {}^{3}\Sigma_g^{-}
- (c) {}^{1}\Sigma_g^{-}
- (d) {}^{3}\Sigma_g^{+}
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Answer: (b)
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Q127 · 2011 · 2 marks
The complex \mathrm{[Mn(H_2O)_6]^{+2}} has very light pink colour. The best reason for it is [CSIR-JUNE 2011]
- (a) the complex does not have a charge transfer transition.
- (b) d-d transitions here are orbital forbidden but spin allowed.
- (c) d-d transitions here are orbital allowed but spin forbidden.
- (d) d-d transitions here are both orbital forbidden and spin forbidden.
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Answer: (d)
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Q128 · 2011 · 2 marks
The number of possible isomers for [\mathrm{Ru(bpy)_2Cl_2}] is (bpy = 2,2′- bipyridine) [CSIR-JUNE 2011]
- (a) 2
- (b) 3
- (c) 4
- (d) 5


(I) trans-form (Optically inactive) (II) d-cis-form (III) l-cis-form
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Answer: (b)
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Q129 · 2011 · 2 marks
The term symbol for the ground state of nitrogen atoms is [CSIR-DEC 2011]
- (a) {}^{3}\mathrm{P}_{0}
- (b) {}^{4}\mathrm{P}_{3/2}
- (c) {}^{1}\mathrm{P}_{1}
- (d) {}^{4}\mathrm{S}_{3/2}
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Answer: (d)
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Q130 · 2011 · 2 marks
The complex that absorbs light of shortest wavelength is [CSIR-DEC 2011]
- (a) [\mathrm{CoF}_{6}]^{3-}
- (b) [\mathrm{Co}(\mathrm{H}_{2}\mathrm{O})_{6}]^{3+}
- (c) [\mathrm{Co}(\mathrm{NH}_{3})_{6}]^{3+}
- (d) [\mathrm{Co}(\mathrm{ox})_{3}]^{3-}\ (\mathrm{ox}=\mathrm{C}_{2}\mathrm{O}_{4}^{2-})
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Answer: (c)
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Q131 · 2011 · 2 marks
Observe the following electronic transition of a diatomic molecule. (A) {}^{1}\Sigma^{+}_{g} \rightarrow {}^{3}\Sigma^{+}_{g} (B) {}^{1}\Sigma^{+}_{u} \rightarrow {}^{1}\Sigma^{+}_{g} (C) {}^{1}\Delta_{u} \rightarrow {}^{1}\Sigma^{+}_{g} (D) {}^{1}\Pi_{g} \rightarrow {}^{1}\Sigma^{+}_{u} The allowed transitions are [CSIR-DEC 2011]
- (a) (A) and (C) only
- (b) (B) and (D) only
- (c) (A), (B) and (C) only
- (d) (A), (C) and (D) only
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Answer: (b)
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Q132 · 2011 · 2 marks
The electronic spectrum of [\mathrm{CrF}_{6}]^{3-} shows three bands at 14,900\ \mathrm{cm}^{-1}, 22400\ \mathrm{cm}^{-1} and 34,800\ \mathrm{cm}^{-1}. The value of \Delta_{\mathrm{o}} in this case is: [CSIR-DEC 2011]
- (a) 5,500\ \mathrm{cm}^{-1}
- (b) 14,900\ \mathrm{cm}^{-1}
- (c) 22,400\ \mathrm{cm}^{-1}
- (d) 34,800\ \mathrm{cm}^{-1}
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Answer: (b)
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Q133 · 2011 · 2 marks
The coordination number and geometry of cerium in \mathrm{[Ce(NO_3)_6]^{-2}} are respectively, [CSIR-DEC 2011]
- (a) 6 and octahedron
- (b) 6 and trigonal prism
- (c) 8 and cubic
- (d) 12 and icosahedron
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Answer: (d)
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Q134 · 2011-2020 · 2 marks
\mathrm{Ni}\left(\mathrm{CN}_{4}\right)^{2-} and \mathrm{Ni}\left(\mathrm{Cl}_{4}\right)^{2-} complex ions are :
- (a) Both diamagnetic.
- (b) Both paramagnetic
- (c) Diamagnetic and paramagnetic respectively
- (d) Antiferromagnetic and diamagnetic respectively
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Answer: (c)
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Q135 · June 2011 · 2 marks
According To Crystal Field Theory, \mathrm{Ni^{2+}} can two have unpaired electrons in
- (a) Octahedral geometry only
- (b) Square planar geometry only
- (c) Tetrahedral geometry only
- (d) Both octahedral and tetrahedral geometry
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Answer: (c)
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Q136 · June 2011 · 2 marks
The term symbol of a molecule with electronic configuration: (1 \sigma \mathrm{~g})^{2}(1 \sigma \mathrm{u})^{2}(2 \sigma \mathrm{~g})^{2}(2 \sigma \mathrm{u})^{2}(1 \pi \mathrm{u})^{1}(1 \pi \mathrm{u})^{1} is:
- (a) { }^{1} \sum{ }^{+}
- (b) { }^{3} \sum \quad-
- (c) { }^{1} \sum \bar{g}
- (d) { }^{3} \sum \quad \begin{array}{l}+ g\end{array}
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Answer: (b)
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Q137 · June 2011 · 2 marks
The complex [\mathrm{Mn}(\mathrm{H}_2\mathrm{O})_6]^{+2} has very light pink colour. The best reason for it is
- (a) the complex does not have a charge transfer transition.
- (b) d-d transitions here are orbital forbidden but spin allowed.
- (c) d-d transitions here are orbital allowed but spin forbidden.
- (d) d-d transitions here are both orbital forbidden and spin forbidden.
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Answer: (d)
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Q138 · June 2011 · 2 marks
The possible J values for { }^{3} \mathrm{D} term symbol are
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Answer: (b)
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Q139 · 2011 · 2 marks
Which of the following compound show a charge-transfer band? [CSIR-JUNE 2011]
- (a) Lanthanum nitrate.
- (b) Ceric ammonium nitrate
- (c) Manganese (II) acetate
- (d) Copper (II) sulphate pentahydrate
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Answer: (b)
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Q140 · Dec 2011 · 2 marks
The term symbol for the ground state of nitrogen atoms is
- (a) {}^{3}\mathrm{P}_{0}
- (b) {}^{4}\mathrm{P}_{3/2}
- (c) {}^{1}\mathrm{P}_{1}
- (d) {}^{4}\mathrm{S}_{3/2}
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Answer: (d)
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Q141 · Dec 2011 · 2 marks
The complex that absorbs light of shortest wavelength is
- (a) \left[\mathrm{CoF}_{6}\right]^{3-}
- (b) \left[\mathrm{Co}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{3+}
- (c) \left[\mathrm{Co}\left(\mathrm{NH}_{3}\right)_{6}\right]^{3+}
- (d) \left[\mathrm{Co}(\mathrm{ox})_{3}\right]^{3-}\left(\mathrm{ox}=\mathrm{C}_{2} \mathrm{O}_{4}{ }^{2-}\right)
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Answer: (c)
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Q142 · 2011 · 2 marks
Green coloured \mathrm{Ni}\left(\mathrm{PPh}_{2} \mathrm{Et}_{2} \mathrm{Br}_{2}\right., has a magnetic moment of 3.20 B.M. The geometry and the number of isomers possible for the complex respectively, are
- (a) Square planar and one
- (b) Tetrahedral and one
- (c) Square planar and two
- (d) Tetrahedral and two
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Answer: (b)
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Q143 · Dec 2011 · 2 marks
Observe the following electronic transition of a diatomic molecule.
- (a) { }^{1} \Sigma^{+}{ }_{\mathrm{g}} \rightarrow^{3} \Sigma^{+}{ }_{\mathrm{g}} (A) and (C) only
- (b) { }^{1} \Sigma^{+}{ }_{\mathrm{u}} \rightarrow{ }^{1} \Sigma^{+}{ }_{\mathrm{g}} (B) and (D) only
- (c) { }^{1} \Delta_{\mathrm{u}} \rightarrow{ }^{1} \Sigma^{+}{ }_{\mathrm{g}} (A), (B) and (C) only
- (d) { }^{1} \pi_{\mathrm{g}} \rightarrow^{1} \Sigma^{+}{ }_{\mathrm{u}} The allowed transitions are (A)(C) and (D) only
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Answer: (b)
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Q144 · Dec 2011 · 2 marks
The electronic spectrum of \left[\mathrm{CrF}_{6}\right]^{3-} shows three bands at 14,900 \mathrm{~cm}^{-1}, 22400 \mathrm{~cm}^{-1} and 34,800 \mathrm{~cm}^{-1}. The value of \Delta_{\mathrm{o}} in this case is:
- (a) 5,500 \mathrm{~cm}^{-1}
- (b) 14,900 \mathrm{~cm}^{-1}
- (c) 22,400 \mathrm{~cm}^{-1}
- (d) 34,800 \mathrm{~cm}^{-1}
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Answer: (b)
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Q145 · 2011 · 2 marks
A true statement about base hydrolysis of \left[\mathrm{Co}\left(\mathrm{NH}_{3}\right)_{5} \mathrm{Cl}\right]^{+2} is:
- (a) It is a first order reaction
- (b) The rate determining step involves the dissociation of chloride in \left[\mathrm{Co}\left(\mathrm{NH}_{3}\right)_{4}\left(\mathrm{NH}_{2}\right) \mathrm{Cl}\right]^{+}
- (c) The rate is independent of the concentration of the base.
- (d) The rate determining step involves the abstraction of a proton from \left[\mathrm{Co}\left(\mathrm{NH}_{3}\right)_{5} \mathrm{Cl}\right]^{+2}
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Answer: (b)
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Q146 · 2011 · 2 marks
For the following outer sphere electron transfer reactions. \begin{array}{l} {\left[\mathrm{Co}\left(\mathrm{NH}_{3}\right)_{6}\right]^{+2}+\left[\mathrm{Co}^{*}\left(\mathrm{NH}_{3}\right)_{6}\right]^{+3} \rightarrow\left[\mathrm{Co}\left(\mathrm{NH}_{3}\right)_{6}\right]_{+3}+\left[\mathrm{Co} *\left(\mathrm{NH}_{3}\right)_{6}\right]^{+2}} {\left[\mathrm{Ru}\left(\mathrm{NH}_{3}\right)_{6}\right]^{+2}+\left[\mathrm{Ru}^{*}\left(\mathrm{NH}_{3}\right)_{6}\right]^{+3} \rightarrow\left[\mathrm{Ru}\left(\mathrm{NH}_{3}\right)_{6}\right]^{+3}+\left[\mathrm{Ru}^{*}\left(\mathrm{NH}_{3}\right)_{6}\right]^{+2}} \end{array}
3 due to - (a) A change from high spin to low spin in \mathrm{Co}^{*} and high spin to low spin in Ru.
- (b) A change from high spin to low spin in Co* and low spin to high spin \mathrm{Ru}^{*}.
- (c) A change from low spin to high spin in \mathrm{Co}^{*} and the low spin state remains unchanged in Ru.
- (d) A change from low spin to high spin in \mathrm{Co}^{*} and high spin to low spin in \mathrm{Ru}^{*}.
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Answer: (c)
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