1. Write IUPAC names of the following  compounds
		        
		          
		            a) [Co (NH3 )5 Cl ] Cl2
		          b) [Cr(NH3 )6 ]3+
		          c) [Ni(NH3 )6 ] Cl2
		          d) [CoCl(NO2)(NH3)4 ] Cl
		           e) [Co(en)2(ONO)2] Cl
		           f) [Cr(NH3 )5(H2O)]3+
		          g) K3 [Co(C2O4)3 ]
		           h) Na3 [Cr(OH)2F4  ]
		           i) [Co(NH3 )6]  [Cr(CN)6 ]
		           j) [Pt(NH3 )2Cl(NH2CH3)] Cl
		           k) [Ni(CO)4 ]
		           l) [CrCl3 (Py)3 ]
	            
		        2. Write the IUPAC name of ionization  isomer of [Co(NH3)5Br ]SO4
		        3. Write the IUPAC name of linkage isomer  of  [Co(en)2(ONO)2 ]Cl
		        4. Write the formula of the following  coordination compounds:
		        
		          a) Tris (ethane-1,2-diamine)cobalt(III)sulphate 
		            b) Amminebromidochloridonitrito-N- platinate(II) 
		            c) Pottasiumtetrachloridopalladate(II) 
		            d) Tetrahydroxozincate
	            
		        5. Explain the following with suitable  examples 
		        
		          a) coordination entity 
		            b) ligand
		            c) coordination number 
		            d) coordination polyhedron 
		            e) homoleptic 
		            f) heterolrptic
	            
		        6. What is meant by unidentate, bidentate  and ambidentate ligands? Give two examples  each.
		        7. Give an example of hexadentate ligand.
		        8. Explain chelation with a suitable  example.
		        9. Write the IUPAC name and indicate the  oxidation state,electronic configuration and  coordination number of the central metal in the complex  [Co (NH3)5 Cl ] Cl2 Also give the primary and secondary valency of the metal. Give the  stereochemistry   and magnetic moment of this complex.
		        10. Mention the limitations of valence bond  theory.
		        11. Using valence bond theory, predict the  structure and the magnetic behavior of the  below given complexes:
		        
		          a) [Fe(CN)6 ]4-
		           b) [Fe(CN)6 ]3-
		           c) [NiCl4]2-
		           d) [Ni(CN)4]2-
		           e) [Cr(NH3)6 ]3+
		           f) [Co(NH3)6 ]3+
		           g) [Ni(CO)4]
		           h) [Fe(CO)5]
		           i) [MnCl4]2-
		           j) [CoF6 ]3-
		           k) [Co(en)3]3+
		           m) [Co(C2O4)3]3-
		           n) [Mn(CN)6 ]3-
		           o) [Ni(NH3)6 ]3+
		           p) [Fe(H2O)6 ]3+
		           q) [Mn(CN)6 ]4-
		           r) [FeF6]3-
		           s) [MnCl6]3-
		           t) [MnBr4]2-
	            
		        12. Name two properties of central metal  ion which enables it to form stable complex  entities.
		        13. A coordination compound has the formula  CoCl3.4NH3. It does not liberate ammonia but  gives precipitate of AgCl with AgNO3 solution. Give the  structural formula and IUPAC name  of the complex.
		        14. Account for the following:
		        
		           a) [Fe(CN)6]4- is diamagnetic while [Fe(CN)6]3- is paramagnetic.
		           b) [NiCl4]2 is tetrahedral while [Ni(CN)4]2- is square planar.
		           c) Hydrated copper sulphate is colored while anhydrous copper sulphate is  colorless.
		           d) [Ti(H2O)6]3+ become colorless on heating.
		           e) [Ni(H2O)6]2+ is green while [Ni(CN)4]2- is colorless.
		           f) [Fe(CN)6]4- and [Fe(H2O)6]2+ show different colors in aqueous solution..
		           g) [Cr(NH3)6]3+ is paramagnetic while[Ni(CN)4]2-  is diamagnetic.
		           h) Tetrahedral complex do not exhibit geometrical isomerism.
	            
		        15. What is the difference between inner  orbital and outer orbital complexes? Illustrate with one  example each.
		        16. How the given factor affect the  stability of complex 
		        
		          a) charge on cation 
		            b) nature of ligand.
	            
		        17. Illustrate the following with an example each:
		        
		           a) linkage isomerism 
		                b) ionization isomerism 
		                  c) coordination isomerism 
		              d)  hydrate isomerism 
		             e) geometrical isomerism 
		             f) optical isomerism
	            
		        18. Draw the geometrical isomers of  [Co(NH3)3(NO2)3]  and label them.
		        19. Give a chemical test to distinguish  between [Co (NH3)5 Cl ] SO4 and [Co (NH3)5 SO4 ] Cl  What type of isomerism does they exhibit?
		        20. Draw the structure of optical isomers  of  
		        
		          a) [Co(en)3]3+
		               b) [Cr(C2O4)3]3-
		               c) [PtCl2(en)2 ]2+
		             d) [Cr(NH3)2 Cl2(en)]+
	            
		        21. Draw the structure of all the isomers  (geometrical and optical) of 
		        
		          a) [CoCl2(en)2]+
		           b) [Co(NH3)2Cl2(en)]+
		          c)  [Co(NH3) Cl (en)2]2+
	            
		        22. A metal ion Mn+ having d4  configuration combine with three didentate ligand to form a complex   compound. Assuming D0>P   
		        
		          i) Draw the diagram showing d orbital splitting during this complex  formation.
		            ii) Write the electronic configuration of  the valence electron of  the metal   Mn+ ion in terms
		            of  t2g and eg.
		            iii) What type of hybridisation will Mn+  ion have?             
		            iv) Draw the structure of isomers exhibited by this complex.
	            
                23. Draw the figure to show the d orbital  splitting in tetrahedral complex.
                24. Mention the limitations of crystal  field theory.
                25. What is spectrochemical series? Explain  the difference between strong and weak ligand.
                26. Calculate the overall complex  dissociation constant of the complex [Cu(NH3)4]2+ b4  for the complex is 2x1013.
                27. The spin only magnetic moment of the  complex[MnBr4]2- is 5.9B.M. Predict the geometry of  the complex. 
                28. Calculate the spin only magnetic moment  of the complex 
                
                  a) [Fe(CN)6]4- 
                  b) [CoF6]3-
                
                29. Aqueous copper sulphate gives green  precipitate with KF(aq) but bright green solution with KCl(aq). Explain these results.
                30. What is the coordination entity formed  when excess of KCN is ttreated with aqueous copper  sulphate. Why is that no precipitate of copper sulphide is formed when H2S  is passed through  this solution?
                31. Give one application each of  coordination compounds in 
                
                  a) analytical chemistry 
                    b) biological system 
                      c) medicine 
                       d) extraction of metal/metallurgy
                     e) estimation of  hardness of water.
                
                32.   Draw the structures of 
                
                  a) [Ni(CO)]4
                  b) [Fe(CO)]5
                  c) [ Cr(CO)]6
                  d) [Mn2(CO)]10
                  e) [Co2(CO)]8. Explain the bonding in metal carbonyls.