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Enumerate the reactions of D-glucose which cannot be explained by its open chain structure.
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- Write structures of different isomeric amines corresponding to the molecular formula C4H11N.
- Write the IUPAC names of all the isomers.
- What type of isomerism is exhibited by different pairs of amines?
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How will you convert Benzene into aniline?
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How will you convert Benzene into N, N-dimethylaniline?
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How will you convert Cl−(CH2)4−Cl into hexan-1, 6-diamine?
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Arrange the following in increasing order of their basic strength:
C2H5NH2, C6H5NH2, NH3, C6H5CH2NH2 and (C2H5)2NH
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Arrange the following in increasing order of their basic strength:
C2H5NH2, (C2H5)2NH, (C2H5)3N, C6H5NH2
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Arrange the following in increasing order of their basic strength:
CH3NH2, (CH3)2NH, (CH3)3N, C6H5NH2, C6H5CH2NH2
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Complete the following acid-base reaction and name the product:
\[\ce{CH3CH2CH2NH2 + HCl ->}\]
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Complete the following acid-base reaction and name the product:
\[\ce{(C2H5)3N + HCl ->}\]
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Account for the following:
Gabriel phthalimide synthesis is preferred for synthesising primary amines.
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Arrange the following:
In increasing order of boiling point:
C2H5OH, (CH3)2NH, C2H5NH2
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Accomplish the following conversion:
Benzene to m-bromophenol
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Accomplish the following conversion:
Aniline to p-bromoaniline
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Give a plausible explanation for the following:
Why are aliphatic amines stronger bases than aromatic amines?
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Complete the following reaction:
\[\ce{C6H5N2Cl + H3PO2 + H2O ->}\]
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Arrange the following compound in increasing order of its reactivity in nucleophilic addition reactions.
Ethanal, Propanal, Propanone, Butanone.
Hint: Consider steric effect and electronic effect.
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Arrange the following compound in increasing order of its reactivity in nucleophilic addition reactions.
Benzaldehyde, p-Tolualdehyde, p-Nitrobenzaldehyde, Acetophenone.
Hint: Consider steric effect and electronic effect.
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Predict the product of the following reaction:

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