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Class 12 Chemistry NCERT Solutions For Chapter 13 Hydrocarbons

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Download NCERT Solutions for Class 12 Chenistry

Chapter 13 Amines

(Link of Pdf file is given below at the end of the Questions List)

In this pdf file you can see answers of following Questions

NCERT Solutions Exercises Questions


Question 13.1 Write IUPAC names of the following compounds and classify them into primary, secondary and tertiary amines.
(i) (CH3)2CHNH2
(ii) CH3(CH2)2NH2
(iii) CH3NHCH(CH3)2
(iv) (CH3)3CNH2
(v) C6H5NHCH3
(vi) (CH3CH2)2NCH3
(vii) m–BrC6H4NH2


Question 13.2 Give one chemical test to distinguish between the following pairs of compounds.
(i) Methylamine and dimethylamine
(ii) Secondary and tertiary amines
(iii) Ethylamine and aniline
(iv) Aniline and benzylamine
(v) Aniline and N-methylaniline.


Question 13.3 Account for the following:
(i) pKb of aniline is more than that of methylamine.
(ii) Ethylamine is soluble in water whereas aniline is not .
(iii) Methylamine in water reacts with ferric chloride to precipitate hydrated ferric oxide.
(iv) Although amino group is o– and p– directing in aromatic electrophilic substitution reactions, aniline on nitration gives a substantial amount of m-nitroaniline.
(v) Aniline does not undergo Friedel-Crafts reaction.
(vi) Diazonium salts of aromatic amines are more stable th
an those of aliphatic amines.
(vii) Gabriel phthalimide synthesis is preferred for synthesising primary amines.


Question 13.4 Arrange the following:
(i) In decreasing order of the pKb values: C2H5NH2, C6H5NHCH3, (C2H5)2NH and C6H5NH2
(ii) In increasing order of basic strength: C6H5NH2, C6H5N(CH3)2, (C2H5)2NH and CH3NH2
(iii) In increasing order of basic strength: (a) Aniline, p-nitroaniline and p-toluidine (b) C6H5NH2, C6H5NHCH3, C6H5CH2NH2.
(iv) In decreasing order of basic strength in gas phase: C2H5NH2, (C2H5)2NH, (C2H5)3N and NH3
(v) In increasing order of boiling point: C2H5OH, (CH3)2NH, C2H5NH2
(vi) In increasing order of solubility in water: C6H5NH2, (C2H5)2NH, C2H5NH2.


Question 13.5 How will you convert:
(i) Ethanoic acid into methanamine
(ii) Hexanenitrile into 1-aminopentane
(iii) Methanol to ethanoic acid
(iv) Ethanamine into methanamine
(v) Ethanoic acid into propanoic acid
(vi) Methanamine into ethanamine
(vii) Nitromethane into dimethylamine
(viii) Propanoic acid into ethanoic acid?


Question 13.6 Describe a method for the identification of primary, secondary and tertiary amines. Also write chemical equations of the reactions involved.


Question 13.7 Write short notes on the following:
(i) Carbylamine reaction
(ii) Diazotisation
(iii) Hofmann’s bromamide reaction
(iv) Coupling reaction
(v) Ammonolysis
(vi) Acetylation
(vii) Gabriel phthalimide synthesis.


Question 13.8 Accomplish the following conversions:
(i) Nitrobenzene to benzoic acid
(ii) Benzene to m-bromophenol
(iii) Benzoic acid to aniline
(iv) Aniline to 2,4,6-tribromofluorobenzene
(v) Benzyl chloride to 2-phenylethanamine
(vi) Chlorobenzene to p-chloroaniline
(vii) Aniline to p-bromoaniline
(viii) Benzamide to toluene
(ix) Aniline to benzyl alcoho


sample paper of chemistry

Question 13.10 An aromatic compound ‘A’ on treatment with aqueous ammonia and heating forms compound ‘B’ which on heating with Br2 and KOH forms a compound ‘C’ of molecular formula C6H7N. Write the structures and IUPAC names of compounds A, B and C.

Question 13.11 Complete the following reactions:
(i) C6H5NH2 + CHCl3 + alc.KOH →
(ii) C6H5N2Cl + H3PO2 + H2O →
(iii) ( ) C6H5NH2 + H2SO4 conc. →
(iv) C6H5N2Cl + C2H5OH →
(v) ( ) C6H5NH2 +Br2 aq →
(vi) ( ) 6 5 2 3 2 C H NH + CH CO O →
(vii) ( ) ( ) 4 2 i HBF 6 5 2 ii NaNO /Cu, C H N Cl Δ→

Question 13.12 Why cannot aromatic primary amines be prepared by Gabriel phthalimide synthesis?

Question 13.13 Write the reactions of (i) aromatic and (ii) aliphatic primary amines with nitrous acid.

Question 13.14 Give plausible explanation for each of the following:
(i) Why are amines less acidic than alcohols of comparable molecular masses?
(ii) Why do primary amines have higher boiling point than tertiary amines?
(iii) Why are aliphatic amines stronger bases than aromatic amines?

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