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Special format questions can be framed from the following topics of this chapter
–Ligands – IUPAC nomenclature
–Isomerism – Valence bond theory
–Werner’s theory – Magnetic properties
A/R, species selection and matching type MCQs can be framed from Ligands.
On IUPAC nomenclature, question based on A/R and 5-Statements type MCQs can be framed
For the topic Valence bond theory, 2-statements, 5-Statements and sepcies selection type MCQs can be
framed.
From magnetic properties, question based on A/R, 2-Statements, species selection and matching type
MCQs can be framed.
1. Assertion (A) All the octahedral complexes of Ni 2+ are outer orbital complexes.
Reason (R) Generally outer orbital octahedral complexes are given by weak field ligands.
3. Assertion (A) tris (ethane-1, 2-diamine) nickel (II) chloride is a homoloeptic outer orbital complex.
Reason (R) The complex tris(ethane-1, 2-diamine) nickel (II) chloride has d 2sp3 hybridisation.
4. Assertion (A) [Co(H 2 NCH 2CH 2 NH 2 )3 ]2 (SO 4 )3 is named as tris (ethane-1, 2-diamine) cobalt (II) sulphate.
Reason (R) Sulphate is the counter anion in this molecule and it takes three sulphates to bond with two
complex cations.
5. Assertion (A) Geometry of any complex depends upon the nature of ligands attached.
Reason (R) (Ni(CO) 4 ] has square planar geometry while [Ni(CN)4 ]2− has tetrahedral geometry.
6. Assertion (A) [CoCl(NH 3 )5 ]2+ absorbs greater energy at lower wavelength of light with respect to
[Co(NH 3 )5 (H 2O)]3+ .
Reason (R) Wavelength of the light absorbed depends on the oxidation state of the metal ion.
7. Assertion (A) The theoretical value of magnetic moment () is 1.73 BM when CN − ligands join Fe 3+ ion
to yield complex
Reason (R) In complex [Fe(CN)6 ]3− , the central metal ion has two unpaired electron.
8. Assertion (A) In [Co(Cl 2 )(en)2 ] coordination number of Co is 4 and this compound has a square planar
geometry.
Reason (R) The coordination number of a central metal atom in a complex is determined by the number of
monodenate ligands around a metal ion bonded by -bonds.
9. Assertion (A) The complex (Ni(en)3 ]Cl 2 , has lower stability than [Ni(NH 3 )6 ]Cl 2 .
Reason (R) In complex [Ni(en)3 ]Cl 2 , the geometry of Ni is octahedral geometry.
10. Statement I [Mn(CN)6 ]3− ,[Fe(CN)6 ]3− and [Co(C2O4 )3 ]3− are d 2sp3 hybridised.
Statement II [MnCl6 ]3− and [FeF6 ]3− are paramagnetic and have 5 and 4 unpaired electrons respectively.
11. Statement I Metal attached with EDTA in an octahedral complex, has a denticity of 4.
Statement II [EDTA]4− bind through two nitrogen and four oxygen atoms to a central metal ion.
12. Statement I For the octahedral complexes of Fe 3+ in SCN − and in CN − ligands, the difference between
the s is 3 B.M.
Statement II SCN − and CN − ion can coordinate only through ‘N’ to a central atom or ion.
13. Statement I The complex [PtCl 2 (NH 3 )(H 2O)] is a diamagnetic complex.
Statement II Complex [PtCl 2 (NH 3 )(H 2O)] can show hydrate isomerism and the hybridisation state of Pt is
sp 3 .
14. Statement I [Ni(H 2O)6 ]2+ and [Ni(NH 3 )6 ]2+ have the same value or magnetic moment.
Statement II Magnetic moment is calculated by using number of paired electron.
22. Among the following, the number of compounds that are diamagnetic in nature is
(i) [FeF6 ]3− (ii) [Co(C2O4 )3 ]3− (iii) [Ni(CN)4 ]2−
(iv) [MnCl6 ]3− (v) [PtCl 2 (NH 3 )(OH 2 )]
(a) 1 (b) 3 (c) 2 (d) 4
23. Consider the following ligands.
(i) NO2− (ii) NO3− (iii) C2O24− (iv) SCN − (v) H 2 NCH 2CH 2 NH 2
The total number of ligands, which are ambidentate in nature is
(a) 4 (b) 3 (c) 1 (d) 2