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 Multiple Choice QuestionsShort Answer Type

171. Draw all the isomers (geometrical and optical) of
[Co(NH3)Cl(en)2 ]2+ 
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172. Draw all the isomers (geometrical and optical) of
[Co(NH3)2Cl2(en)]+
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173. Write all the geometrical isomers of[Pt(NH3)(Br)Cl(py)] and how many of these will exhibit optical isomers? 
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174. 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.
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175. 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 H2S(g) is passed through this solution?  
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176.

Draw figure to show splitting of d orbitals in an octahedral crystal field.


Crystal field effects in octahedral coordination entities:

(i) Let us assume that the six ligands are positioned symmetrically along the cartesian axes, with metal atom at the origin. As the ligands approach first there is an increase in energy of d-orbitals relative to that of the free ion just as would be the case in a spherical field.

(ii) The orbitals lying along the axes (dz2 , and dx2– y2) get repelled more strongly than d xy’, d yz. and d zx orbitals which have lobes directed between the axes.


Fig. d-orbital splitting in an octahedral crystal field.

The dz2 , and dx2– y2 orbitals get raised in energy and dxy, dyz, dxz orbitals are lowered in energy relative to the average energy in the spherical crystal field.

Thus, the degenerate set of d-orbitals get split into two sets: the lower energy orbitals set t2g and the higher field energy orbitals eg set. The energy is separated by Δ0.

 

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177.

What is spectrochemical series? Explain the difference between a weak field ligand and a strong field ligand.

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178. Discuss the nature of bonding in the following coordination entities on the basis of valence bond theory. 
 [Fe(CN)6]4–  
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179. Discuss the nature of bonding in the following coordination entities on the basis of valence bond theory. 
[FeF6]3–
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180. Discuss the nature of bonding in the following coordination entities on the basis of valence bond theory. 
 [CoF6]3–
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