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CH 5 S Cbse M
CH 5 S Cbse M
CH 5 S Cbse M
Ans.- (d)
Ans.- (a)
Ans.- (a)
Ans.- (d)
Ans.- (c)
Ans: (a)
Ans-
(a). 6.
(b). Homoleptic
(c). Ligand
(d). 6, +2.
(e). Complex salts .
Ans.
(a) (iii)
(b) (i)
(c) (iv)
(d) (ii)
Ans.- AgBr forms a complex ion, [Ag(S2O3)2]3– when it is washed with hypo
solution in black and white photography
.Ans. [Co(en)3]3+ is more stable complex than [CO(NH3)6]3+ due to chelate effect .
Q.13 Write the IUPAC name of the following coordination compound [NiCl4]2-
Q.15. Give the coordination number of the central metal ion in the following
complexes
(i) (NH4)2[CoF4]
(ii) [Mn(H20)6]SO4
Q.19.Amongst the following ions? Which one has the highest magnetic moment
value:
(i) [Cr(H2O)6]3+
(ii) [Fe(H20)6]2+ (iii) [Zn(H20)6]2+
Ans.- μ=√n(n+2)
where n is number of unpaiared electrons
No of unpaired electron = 3
in [Fe(H20)6]2+ electronic configuration of Fe2+ = 3d6,
no of unpaired electron = 4
in [Zn(H20)6]2+ Electronic configuration ofZn2+ = 3d10,
Q.20. Write down the IUPAC name for each of the following complexes and indicate
the oxidation state and coordination number. (i) K[Cr(H20)2(C204)2|-3H20 (ii)
[Co(NH3)5CIlCl2
Ans.-(i) K[Cr(H20)2(C204)2|-3H20
(ii) [Co(NH3)5CIlCl2
IUPAC name is pentaamminechloridocobalt (III) chloride Coordination number of
Co = 6
Oxidation state of Co, x + 0 -1 = + 2 .’. x = + 3
Ans.- low spin tetrahedral complexes not formed because orbital splitting energies
for tetrahedral complexes are large to force pairing.
Ans.- (i) Copper atom has completely filled d orbitals (3d 10) in its ground state, yet it
is regarded as a transition element due to incompletely filled d-orbital in its ionic
states i.e. Cu2+ (3d9).
(ii) The highest oxidation state for Cr is +6, therefore it can loose 3 more electrons,
whereas Fe needs to loose only 1 electron to achieve its highest oxidation state of +3.
Thus, Cr3+ is more reducing than Fe2+
Q .24 Explain why Nickel does not form low spin octahedral complexes?
Ans.- CN is a strong field ligand and H2O is a weak field ligand, in both compound
[Fe(H2O)6]3+ and [Fe(CN)6]3- oxidation state of Fe is +3.
In [Fe(CN)6]3-, the 3d electrons are paired up, hybridisation d2sp3. It forms an inner
orbital complex and is weakly paramagnetic.