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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.

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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–  


[Fe(CN)6]4 –

Outer electronic configuration of iron (Z = 26) in ground state is 3d64s2. Iron in this complex is in +2 oxidation state. Iron achieves +2 oxidation state by the loss of two 4s electrons. The resulting Fe2+ ion has outer electronic configuration of 3d6.
Since CN- is strong field ligand thus cause pairing.


It has been experimentally observed that this complex is diamagnetic as such has no unpaired electron. To account for this two unpaired electrons in the 3d - subshell pair up, thus leaving two 3d-orbitals empty. These two vacant 3d-orbitals along with one 4s-orbital and three 4p-orbitals hybridise to give six equivalent d2sp3 hybridised orbitals. Six pairs of electrons, one from each cyanide ion, occupy the six vacant hybrid orbitals so produced. The resulting complex ion has an octahedral geometry and is diamagnetic due to the absence of unpaired electrons.

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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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