Coordination WS Key
Coordination WS Key
Coordination WS Key
1. (b)
CuSO 4 +4 NH 3 →[Cu( NH 3 )4 ]SO 4
10. (c) It gives precipitate with
AgNO
3 it means it given Cl
−
2. (b) Oxalate is a bidentate ligand hence forms a chelate. ion in the solutions. Since conductivity corresponds to two
−
ions, it shows one Cl is outside the coordination sphere. The
structure will be
[Cr ( H 2 O )4 Cl 2 ]Cl→[Cr ( H 2 O)4 Cl 2 ]+ +Cl−
−
3. (a) Oxidations state of Mn in
[ MnO 4 ] = +7, hence it does AgNO 3 +Cl− → AgCl +NO −3
not have any d-electron present in it. White ppt
0 0
Mn7 + (Z = 25) : [ Ar ]4 s 3d
[Co( NH 3 )5 SO 4 ]Br →[Co( NH 3 )5 SO4 ]+ +Br −
(d) In the complex linkage, geometrical and optical isomerism 11.
X
4.
are possible. AgNO 3 +Br− → AgBr +NO−3
pale yellow
of the complex is
[Co( NH 3 )6 ]Cl 3 .
No. of unpaired electrons = 0.
Hence, shows no paramagnetism. 13. (a) SCN and
− NO−
2 are ambidentate ligand since they have
more than one donor atoms to attach to the central metal
6 atom.
7. (c) In d (low spin) electrons get paired up to make two d-
orbitals empty. Hydridisations is d 2 sp 3 (octahedral) and the 14. (a) Potassium pentacyanonitrosylferrate (II)
complex is low spin.
15. (b) The ligand are interchanged in both the cationic and
8. (c) Cr is in zero oxidations state. anionic entities of different metal ions present in a complex to
form coordination isomers.
23. (a)
Number of unpaired e- = 4 24 BM
[Co(C2O4)3]3- : Co3+ = 3d6 ( 0 > P)
30. (b)
[Co(NH3)5SO4]Br+AgNO3 AgBr
0.01 mol excess 0.01 Mol
[Co(NH3)5Br]SO4+BaCl2 BaSO4
26. (d) 0.01 mol excess 0.01 Mol
Crystal field theory introduce
spectrochemical series based upon the
experimental values of but can't explain
it's order. While other three points arc
explained by CFT. Specially when the CFSE
increases thermodynamic stability of the
complex increases.
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