CBSE Class 12 Chemistry Chapter 9 Important Questions – Free PDF Download
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Important Questions Class 12 Chemistry Chapter 9 – Coordination Compounds
CBSE Class 12 Chemistry Important Questions Chapter 9 – Coordination Compounds
3 Marks Questions
1.What is geometric isomerism? When can a compound show.
(1) Cis – Trans isomerism
(2) Fac and Mer isomerism.
Ans.The isomerism that arises in hetroleptic complexes due to different possible geometric arrangements of the ligands is called geometric isomerism.
1) Cis and Trans isomerism can occur in square planar complexes of formula 
( X&L are unidentate ligands), square planar complexes of formula MAB X L & octahedral complexes of formula
.
2) Fac and mer isomerism can occur in octahedral complexes of formula
.
2.How do optical isomer differ from each other?
Ans.Optical isomers differ in the direction in which they rotate the plane of polarized light in a polarimeter.
3.Make the cis and trans forms of the complex 
. Which one of these will be optically active?
Ans.
Cis and trans forms.
The cis form will be optically active.
mirror
4.Which isomerism is shown by a compound having ambidentate ligand? Give example.
Ans.A complex having ambident ligand will show linkage isomerism e.g 
as ambident Ligand and its Linkage isomer will be 
.
5.What is ionization isomerism? Give an example.
Ans.Ionisation isomerism arises when the counter ion in a complex salt is itself a potential Ligand and can displace a Ligand which can then become counter ion e.g. 
and 
are ionization isomer.
6.How do solvate isomers differ from each other?
Ans.The solvate isomers differ by wether or not a solvent molecule is directly bonded to the metal ion or is merely present on free solvent molecules in the crystal.
7.Draw the geometrical isomers of
?
Ans.Geometrical isomers
8.Give evidence that 
and 
are ionization isomers.
Ans.When ionization isomers are dissolved in water, they ionize to give different ions. These ions then react differently with different reagents to give different products.
9. The hexaquo manganese (II) ion contains five unpaired electrons, while the hexacyanoion contains only one unpaired electron. Explain using Crystal Field Theory.
Ans.
 |  |
| Mn is in the +2 oxidation state. | Mn is in the +2 oxidation state. |
The electronic configuration is  . | The electronic configuration is . |
| The crystal field is octahedral. Water is a weak field ligand. Therefore, the arrangement of the electrons in is t2g3eg2. | The crystal field is octahedral. Cyanide is a strong field ligand. Therefore, the arrangement of the electrons in isT2g5eg0. |
Hence, hexaaquo manganese (II) ion has five unpaired electrons, while hexacyano ion has only one unpaired electron.
10. Calculate the overall complex dissociation equilibrium constant for the 
ion, given that 
for this complex is 
Ans.=
The overall complex dissociation equilibrium constant is the reciprocal of the overall stability constant,.
11. Explain the bonding in coordination compounds in terms of Werner’s postulates.
Ans.Werner’s postulates explain the bonding in coordination compounds as follows:
(i) A metal exhibits two types of valencies namely, primary and secondary valencies. Primary valencies are satisfied by negative ions while secondary valencies are satisfied by both negative and neutral ions.
(In modern terminology, the primary valency corresponds to the oxidation number of the metal ion, whereas the secondary valency refers to the coordination number of the metal ion.
(ii) A metal ion has a definite number of secondary valencies around the central atom. Also, these valencies project in a specific direction in the space assigned to the definite geometry of the coordination compound.
(iii) Primary valencies are usually ionizable, while secondary valencies are non-ionizable.
12.How many geometrical isomers are possible in the following coordination entities?
(i) 
(ii) 
Ans.(i) For , no geometric isomer is possible as it is a bidentate ligand.
(ii)
Two geometrical isomers are possible.
13.Aqueous copper sulphate solution (blue in colour) gives:
(i) a green precipitate with aqueous potassium fluoride, and
(ii) a bright green solution with aqueous potassium chloride
Explain these experimental results.
Ans.Aqueous 
exists as 
. It is blue in colour due to the presence of
ions.
(i) When KF is added:
(ii) When KCl is added:
In both these cases, the weak field ligand water is replaced by the 
and 
ions.
14. What is the coordination entity formed when excess of aqueous KCN is added to an aqueous solution of copper sulphate? Why is it that no precipitate of copper sulphide is obtained when 
is passed through this solution?
Ans.
i.e., 
Thus, the coordination entity formed in the process is 
. is a very stable complex, which does not ionize to give 
ions when added to water. Hence, ions are not precipitated when 
is passed through the solution.
15.Draw figure to show the splitting of d orbitals in an octahedral crystal field.
Ans.
The splitting of the d orbitals in an octahedral field takes palce in such a way that 
experience a rise in energy and form the 
level, while 
and
experience a fall in energy and form the 
level.
16.What is meant by the chelate effect? Give an example.
Ans.When a ligand attaches to the metal ion in a manner that forms a ring, then the metal- ligand association is found to be more stable. In other words, we can say that complexes containing chelate rings are more stable than complexes without rings. This is known as the chelate effect.
For example:
17.Amongst the following ions which one has the highest magnetic moment value?
(i) 
(ii) 
(iii) 
Ans.(i) No. of unpaired electrons in = 3
Then, 
(ii) No. of unpaired electrons in = 4
Then, 
(iii) No. of unpaired electrons in 
Hence, has the highest magnetic moment value.
18.What will be the correct order for the wavelengths of absorption in the visible region for the following: 
Ans.The central metal ion in all the three complexes is the same. Therefore, absorption in the visible region depends on the ligands. The order in which the CFSE values of the ligands increases in the spectrochemical series is as follows:
Thus, the amount of crystal-field splitting observed will be in the following order:
Hence, the wavelengths of absorption in the visible region will be in the order:
