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NCERT solutions for Chemistry Part 1 and 2 [English] Class 12 chapter 9 - Amines [Latest edition]

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NCERT solutions for Chemistry Part 1 and 2 [English] Class 12 chapter 9 - Amines - Shaalaa.com
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Solutions for Chapter 9: Amines

Below listed, you can find solutions for Chapter 9 of CBSE, Karnataka Board PUC NCERT for Chemistry Part 1 and 2 [English] Class 12.


Intext QuestionsExercises
Intext Questions [Pages 262 - 277]

NCERT solutions for Chemistry Part 1 and 2 [English] Class 12 9 Amines Intext Questions [Pages 262 - 277]

Intext Questions | Q 9.1 (i) | Page 262

Classify the following amine as primary, secondary or tertiary:

  • Primary

  • Secondary

  • Tertiary

Intext Questions | Q 9.1 (ii) | Page 262

Classify the following amine as primary, secondary or tertiary:

  • Primary

  • Secondary

  • Tertiary

Intext Questions | Q 9.1 (iii) | Page 262

Classify the following amine as primary, secondary or tertiary:

(C2H5)2CHNH2

  • Primary

  • Secondary

  • Tertiary

Intext Questions | Q 9.1 (iv) | Page 262

Classify the following amine as primary, secondary or tertiary:

(C2H5)2NH

  • Primary

  • Secondary

  • Tertiary

Intext Questions | Q 9.2 | Page 262
  1. Write structures of different isomeric amines corresponding to the molecular formula C4H11N.
  2. Write the IUPAC names of all the isomers.
  3. What type of isomerism is exhibited by different pairs of amines?
Intext Questions | Q 9.3 (i) | Page 265

How will you convert Benzene into aniline?

Intext Questions | Q 9.3 (ii) | Page 265

How will you convert Benzene into N, N-dimethylaniline?

Intext Questions | Q 9.3 (iii) | Page 265

How will you convert Cl−(CH2)4−Cl into hexan-1, 6-diamine?

Intext Questions | Q 9.4 (i) | Page 274

Arrange the following in increasing order of their basic strength:

C2H5NH2, C6H5NH2, NH3, C6H5CH2NH2 and (C2H5)2NH

Intext Questions | Q 9.4 (ii) | Page 274

Arrange the following in increasing order of their basic strength:

C2H5NH2, (C2H5)2NH, (C2H5)3N, C6H5NH2

Intext Questions | Q 9.4 (iii) | Page 274

Arrange the following in increasing order of their basic strength:

CH3NH2, (CH3)2NH, (CH3)3N, C6H5NH2, C6H5CH2NH2

Intext Questions | Q 9.5 (i) | Page 274

Complete the following acid-base reaction and name the product:

\[\ce{CH3CH2CH2NH2 + HCl ->}\]

Intext Questions | Q 9.5 (ii) | Page 274

Complete the following acid-base reaction and name the product:

\[\ce{(C2H5)3N + HCl ->}\]

Intext Questions | Q 9.6 | Page 274

Write reactions of the final alkylation product of aniline with excess of methyl iodide in the presence of sodium carbonate solution.

Intext Questions | Q 9.7 | Page 274

Write chemical reaction of aniline with benzoyl chloride and write the name of the product obtained. 

Intext Questions | Q 9.8 | Page 274

Write structures of different isomers corresponding to the molecular formula C3H9N. Write the IUPAC names of the isomers which will liberate nitrogen gas on treatment with nitrous acid.

Intext Questions | Q 9.9 (i) | Page 277

Convert 3-Methylaniline into 3-nitrotoluene.

Intext Questions | Q 9.9 (ii) | Page 277

Convert aniline into 1, 3, 5-tribromobenzene.

Exercises [Pages 278 - 280]

NCERT solutions for Chemistry Part 1 and 2 [English] Class 12 9 Amines Exercises [Pages 278 - 280]

Exercises | Q 9.1 (i) | Page 278

Write the IUPAC name of the following compound and classify it as primary, secondary and tertiary amine.

(CH3)2CHNH2

  • Primary

  • Secondary

  • Tertiary

Exercises | Q 9.1 (ii) | Page 278

Write the IUPAC name of the following compound and classify it as primary, secondary and tertiary amine.

CH3(CH2)2NH2

  • Primary

  • Secondary

  • Tertiary

Exercises | Q 9.1 (iii) | Page 278

Write the IUPAC name of the following compound and classify it as primary, secondary and tertiary amine.

CH3NHCH(CH3)2

  • Primary

  • Secondary

  • Tertiary

Exercises | Q 9.1 (iv) | Page 278

Write the IUPAC name of the following compound and classify it as primary, secondary and tertiary amine.

(CH3)3CNH2

  • Primary

  • Secondary

  • Tertiary

Exercises | Q 9.1 (v) | Page 278

Write the IUPAC name of the following compound and classify it as primary, secondary and tertiary amine.

C6H5NHCH3

  • Primary

  • Secondary

  • Tertiary

Exercises | Q 9.1 (vi) | Page 278

Write the IUPAC name of the following compound and classify it as primary, secondary and tertiary amine.

(CH3CH2)2NCH3

  • Primary

  • Secondary

  • Tertiary

Exercises | Q 9.1 (vii) | Page 278

Write the IUPAC name of the following compound and classify it as primary, secondary and tertiary amine.

m−BrC6H4NH2

  • Primary

  • Secondary

  • Tertiary

Exercises | Q 9.2 (i) | Page 278

Give one chemical test to distinguish between the following pair of compounds.

Methylamine and dimethylamine

Exercises | Q 9.2 (ii) | Page 278

Give one chemical test to distinguish between the following pair of compounds.

Secondary and tertiary amines

Exercises | Q 9.2 (iii) | Page 278

Give one chemical test to distinguish between the following pair of compounds.

Ethylamine and aniline

Exercises | Q 9.2 (iv) | Page 278

Give one chemical test to distinguish between the following pair of compounds.

Aniline and benzylamine

Exercises | Q 9.2 (v) | Page 278

Give one chemical test to distinguish between the following pair of compounds.

Aniline and N-methylaniline

Exercises | Q 9.3 (i) | Page 278

Account for the following:

pKb of aniline is more than that of methylamine.

Exercises | Q 9.3 (ii) | Page 278

Account for the following:

Ethylamine is soluble in water, whereas aniline is not.

Exercises | Q 9.3 (iii) | Page 278

Account for the following:

Methylamine in water reacts with ferric chloride to precipitate hydrated ferric oxide.

Exercises | Q 9.3 (iv) | Page 278

Account for the following:

Although the amino group is o, p-directing in aromatic electrophilic substitution reactions, aniline on nitration gives a substantial amount of m-nitroaniline.

Exercises | Q 9.3 (v) | Page 278

Give reasons for the following:

Aniline does not undergo Friedel- Crafts reaction.

Exercises | Q 9.3 (vi) | Page 278

Account for the following:

Diazonium salts of aromatic amines are more stable than those of aliphatic amines.

Exercises | Q 9.3 (vii) | Page 278

Account for the following:

Gabriel phthalimide synthesis is preferred for synthesising primary amines.

Exercises | Q 9.4 (i) | Page 278

Arrange the following:

In decreasing order of the pKb values:

C2H5NH2, C6H5NHCH3, (C2H5)2NH and C6H5NH2

Exercises | Q 9.4 (ii) | Page 278

Arrange the following:

In increasing order of basic strength:

C6H5NH2, C6H5N(CH3)2, (C2H5)2NH and CH3NH2

Exercises | Q 9.4 (iii) (a) | Page 278

Arrange the following:

In increasing order of basic strength:

Aniline, p-nitroaniline and p-toluidine

Exercises | Q 9.4 (iii) (b) | Page 279

Arrange the following:

In increasing order of basic strength:

C6H5NH2, C6H5NHCH3, C6H5CH2NH2

Exercises | Q 9.4 (iv) | Page 279

Arrange the following:

In decreasing order of basic strength in the gas phase:

C2H5NH2, (C2H5)2NH, (C2H5)3N and NH3

Exercises | Q 9.4 (v) | Page 279

Arrange the following:

In increasing order of boiling point:

C2H5OH, (CH3)2NH, C2H5NH2

Exercises | Q 9.4 (vi) | Page 279

Arrange the following:

In increasing order of solubility in water:

C6H5NH2, (C2H5)2NH, C2H5NH2

Exercises | Q 9.5 (i) | Page 279

How will you convert ethanoic acid into methanamine?

Exercises | Q 9.5 (ii) | Page 279

How will you convert hexanenitrile into 1-aminopentane?

Exercises | Q 9.5 (iii) | Page 279

How will you convert methanol to ethanoic acid?

Exercises | Q 9.5 (iv) | Page 279

How will you convert ethanamine into methanamine?

Exercises | Q 9.5 (v) | Page 279

How will you convert ethanoic acid into propanoic acid?

Exercises | Q 9.5 (vi) | Page 279

How will you convert methanamine into ethanamine?

Exercises | Q 9.5 (vii) | Page 279

How will you convert nitromethane into dimethylamine?

Exercises | Q 9.5 (viii) | Page 279

How will you convert propanoic acid into ethanoic acid?

Exercises | Q 9.6 | Page 279

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

Exercises | Q 9.7 (i) | Page 279

Write a short note on the following:

Carbylamine reaction

Exercises | Q 9.7 (ii) | Page 279

Write a short note on diazotisation.

Exercises | Q 9.7 (iii) | Page 279

Write a short note on the following:

Hoffmann’s bromamide reaction

Exercises | Q 9.7 (iv) | Page 279

Write a short note on the following:

Coupling reaction

Exercises | Q 9.7 (v) | Page 279

Write a short note on ammonolysis.

Exercises | Q 9.7 (vi) | Page 279

Write short notes on acetylation.

Exercises | Q 9.7 (vii) | Page 279

Write a short note on the following:

Gabriel phthalimide synthesis

Exercises | Q 9.8 (i) | Page 279

Accomplish the following conversion:

Nitrobenzene to benzoic acid

Exercises | Q 9.8 (ii) | Page 279

Accomplish the following conversion:

Benzene to m-bromophenol

Exercises | Q 9.8 (iii) | Page 279

Accomplish the following conversion:

Benzoic acid to aniline

Exercises | Q 9.8 (iv) | Page 279

Accomplish the following conversion:

Aniline to 2, 4, 6-tribromofluorobenzene

Exercises | Q 9.8 (v) | Page 279

Accomplish the following conversion:

Benzyl chloride to 2-phenylethanamine

Exercises | Q 9.8 (vi) | Page 279

Accomplish the following conversion:

Chlorobenzene to p-chloroaniline

Exercises | Q 9.8 (vii) | Page 279

Accomplish the following conversion:

Aniline to p-bromoaniline

Exercises | Q 9.8 (viii) | Page 279

Accomplish the following conversion:

Benzamide to toluene

Exercises | Q 9.8 (ix) | Page 279

Accomplish the following conversion:

Aniline to benzyl alcohol

Exercises | Q 9.9 (i) | Page 279

Give the structure of A, B and C in the following reaction:

\[\ce{CH3CH2I ->[NaCN] A ->[OH-][Partial hydrolysis] B ->[NaOH + Br2] C}\]

Exercises | Q 9.9 (ii) | Page 279

Give the structure of A, B and C in the following reaction:

\[\ce{C6H5N2Cl ->[CuCN] A ->[H2O/H+] B ->[NH3][\Delta] C}\]

Exercises | Q 9.9 (iii) | Page 279

Give the structure of A, B and C in the following reaction:

\[\ce{CH3CH2Br ->[KCN] A ->[LiAlH4] B ->[HNO2][0^\circ C] C}\]

Exercises | Q 9.9 (iv) | Page 279

Give the structure of A, B and C in the following reaction:

\[\ce{C6H5NO2 ->[Fe/HCl] A ->[NaNO2 + HCl][273 K] B ->[H2O/H+][\Delta] C}\]

Exercises | Q 9.9 (v) | Page 279

Give the structures of A, B and C in the following reaction:

\[\ce{CH3COOH ->[NH3][\Delta] A ->[NaOBr] B ->[NaNO2/HCl] C}\]

Exercises | Q 9.9 (vi) | Page 279

Give the structures of A, B and C in the following reaction:

\[\ce{C6H5NO2 ->[Fe/HCl] A ->[HNO2][273 K] B ->[C6H5OH] C}\]

Exercises | Q 9.10 | Page 280

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.

Exercises | Q 9.11 (i) | Page 280

Complete the following reaction:

\[\ce{C6H5NH2 + CHCl3 + alc. KOH ->}\]

Exercises | Q 9.11 (ii) | Page 280

Complete the following reaction:

\[\ce{C6H5N2Cl + H3PO2 + H2O ->}\]

Exercises | Q 9.11 (iii) | Page 280

Complete the following reaction:

\[\ce{C6H5NH2 + H2SO4 (conc.)}\]

Exercises | Q 9.11 (iv) | Page 280

Complete the following reaction:

\[\ce{C6H5N2Cl + C2H5OH ->}\]

Exercises | Q 9.11 (v) | Page 280

Complete the following reaction:

\[\ce{C6H5NH2 + Br2 (aq) ->}\]

Exercises | Q 9.11 (vi) | Page 280

Complete the following reaction:

\[\ce{C6H5NH2 + (CH3CO)2O ->}\]

Exercises | Q 9.11 (vii) | Page 280

Complete the following reaction:

\[\ce{C6H5N2Cl ->[(i) HBF4][(ii) NaNO2/Cu, \Delta]}\]

Exercises | Q 9.12 | Page 280

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

Exercises | Q 9.13 (i) | Page 280

Write the reaction of aromatic primary amine with nitrous acid.

Exercises | Q 9.13 (ii) | Page 280

Write the reaction of aliphatic primary amine with nitrous acid.

Exercises | Q 9.14 (i) | Page 280

Give a plausible explanation for the following:

Why are amines less acidic than alcohols of comparable molecular masses?

Exercises | Q 9.14 (ii) | Page 280

Give a plausible explanation for the following:

Why do primary amines have higher boiling points than tertiary amines?

Exercises | Q 9.14 (iii) | Page 280

Give a plausible explanation for the following:

Why are aliphatic amines stronger bases than aromatic amines?

Solutions for 9: Amines

Intext QuestionsExercises
NCERT solutions for Chemistry Part 1 and 2 [English] Class 12 chapter 9 - Amines - Shaalaa.com

NCERT solutions for Chemistry Part 1 and 2 [English] Class 12 chapter 9 - Amines

Shaalaa.com has the CBSE, Karnataka Board PUC Mathematics Chemistry Part 1 and 2 [English] Class 12 CBSE, Karnataka Board PUC solutions in a manner that help students grasp basic concepts better and faster. The detailed, step-by-step solutions will help you understand the concepts better and clarify any confusion. NCERT solutions for Mathematics Chemistry Part 1 and 2 [English] Class 12 CBSE, Karnataka Board PUC 9 (Amines) include all questions with answers and detailed explanations. This will clear students' doubts about questions and improve their application skills while preparing for board exams.

Further, we at Shaalaa.com provide such solutions so students can prepare for written exams. NCERT textbook solutions can be a core help for self-study and provide excellent self-help guidance for students.

Concepts covered in Chemistry Part 1 and 2 [English] Class 12 chapter 9 Amines are Introduction of Amines, Classification of Amines, Structure of Amines, Physical Properties of Amines, Nomenclature of Animes, Uses of Amines, Identification of Primary, Secondary and Tertiary Amines, Cyanides and Isocyanides, Introduction of Diazonium Salts, Method of Preparation of Diazonium Salts, Importance of Diazonium Salts in Synthesis of Aromatic Compounds, Preparation of Amines, Chemical Reactions of Amines - Basic Character of Amines, Chemical Reactions of Amines - Alkylation and Acylation, Chemical Reactions of Amines - Carbylamine Reaction, Chemical Reactions of Amines - Reaction with Nitrous Acid, Chemical Reactions of Amines - Reaction with Arylsulphonyl Chloride, Chemical Reactions of Amines - Electrophilic Substitution, Physical Properties of Diazonium Salts, Chemical Reaction of Diazonium Salts - Reactions Involving Displacement of Nitrogen, Chemical Reaction of Diazonium Salts - Reactions Involving Retention of Diazo Group, Organic Compounds Containing Nitrogen Numericals, Overview of Amines, Introduction of Amines, Classification of Amines, Structure of Amines, Physical Properties of Amines, Nomenclature of Animes, Uses of Amines, Identification of Primary, Secondary and Tertiary Amines, Cyanides and Isocyanides, Introduction of Diazonium Salts, Method of Preparation of Diazonium Salts, Importance of Diazonium Salts in Synthesis of Aromatic Compounds, Preparation of Amines, Chemical Reactions of Amines - Basic Character of Amines, Chemical Reactions of Amines - Alkylation and Acylation, Chemical Reactions of Amines - Carbylamine Reaction, Chemical Reactions of Amines - Reaction with Nitrous Acid, Chemical Reactions of Amines - Reaction with Arylsulphonyl Chloride, Chemical Reactions of Amines - Electrophilic Substitution, Physical Properties of Diazonium Salts, Chemical Reaction of Diazonium Salts - Reactions Involving Displacement of Nitrogen, Chemical Reaction of Diazonium Salts - Reactions Involving Retention of Diazo Group, Organic Compounds Containing Nitrogen Numericals, Overview of Amines.

Using NCERT Chemistry Part 1 and 2 [English] Class 12 solutions Amines exercise by students is an easy way to prepare for the exams, as they involve solutions arranged chapter-wise and also page-wise. The questions involved in NCERT Solutions are essential questions that can be asked in the final exam. Maximum CBSE, Karnataka Board PUC Chemistry Part 1 and 2 [English] Class 12 students prefer NCERT Textbook Solutions to score more in exams.

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