To give the explanation for aminolysis reaction of propionyl chloride and methylamine when one and two equivalents of methylamine is used. Concept introduction: Amine and acid chloride reacts to produce amide. In this reaction ofAcid chlorides and amine, a proton is also produced which protonates the unreacted amines . The protonated amine loses its nucleophilic property, as a result, it can’t react with acid chloride. To ensure the formation of amide we required twice the number of moles amine as the number of the acid chloride.

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Answer 1

Question

Chapter 16, Problem 63P

Interpretation Introduction

Interpretation:

To give the explanation for aminolysis reaction of propionyl chloride and methylamine when one and two equivalents of methylamine is used.

Concept introduction:

Amine and acid chloride reacts to produce amide. In this reaction ofAcid chlorides and amine, a proton is also produced which protonates the unreacted amines. The protonated amine loses its nucleophilic property, as a result, it can’t react with acid chloride. To ensure the formation of amide we required twice the number of moles amine as the number of the acid chloride.

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Answer 2

Question

Chapter 16, Problem 63P

Interpretation Introduction

Interpretation:

To give the explanation for aminolysis reaction of propionyl chloride and methylamine when one and two equivalents of methylamine is used.

Concept introduction:

Amine and acid chloride reacts to produce amide. In this reaction ofAcid chlorides and amine, a proton is also produced which protonates the unreacted amines. The protonated amine loses its nucleophilic property, as a result, it can’t react with acid chloride. To ensure the formation of amide we required twice the number of moles amine as the number of the acid chloride.

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Answer 3

Question

Chapter 16, Problem 63P

Interpretation Introduction

Interpretation:

To give the explanation for aminolysis reaction of propionyl chloride and methylamine when one and two equivalents of methylamine is used.

Concept introduction:

Amine and acid chloride reacts to produce amide. In this reaction ofAcid chlorides and amine, a proton is also produced which protonates the unreacted amines. The protonated amine loses its nucleophilic property, as a result, it can’t react with acid chloride. To ensure the formation of amide we required twice the number of moles amine as the number of the acid chloride.

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Answer 4

Question

Chapter 16, Problem 63P

Interpretation Introduction

Interpretation:

To give the explanation for aminolysis reaction of propionyl chloride and methylamine when one and two equivalents of methylamine is used.

Concept introduction:

Amine and acid chloride reacts to produce amide. In this reaction ofAcid chlorides and amine, a proton is also produced which protonates the unreacted amines. The protonated amine loses its nucleophilic property, as a result, it can’t react with acid chloride. To ensure the formation of amide we required twice the number of moles amine as the number of the acid chloride.

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Answer 5

Chapter 16, Problem 63P

Interpretation Introduction

Interpretation:

To give the explanation for aminolysis reaction of propionyl chloride and methylamine when one and two equivalents of methylamine is used.

Concept introduction:

Amine and acid chloride reacts to produce amide. In this reaction ofAcid chlorides and amine, a proton is also produced which protonates the unreacted amines. The protonated amine loses its nucleophilic property, as a result, it can’t react with acid chloride. To ensure the formation of amide we required twice the number of moles amine as the number of the acid chloride.

Answer 6

Chapter 16, Problem 63P

Interpretation Introduction

Interpretation:

To give the explanation for aminolysis reaction of propionyl chloride and methylamine when one and two equivalents of methylamine is used.

Concept introduction:

Amine and acid chloride reacts to produce amide. In this reaction ofAcid chlorides and amine, a proton is also produced which protonates the unreacted amines. The protonated amine loses its nucleophilic property, as a result, it can’t react with acid chloride. To ensure the formation of amide we required twice the number of moles amine as the number of the acid chloride.

Answer 7

Chapter 16, Problem 63P

Interpretation Introduction

Interpretation:

To give the explanation for aminolysis reaction of propionyl chloride and methylamine when one and two equivalents of methylamine is used.

Concept introduction:

Amine and acid chloride reacts to produce amide. In this reaction ofAcid chlorides and amine, a proton is also produced which protonates the unreacted amines. The protonated amine loses its nucleophilic property, as a result, it can’t react with acid chloride. To ensure the formation of amide we required twice the number of moles amine as the number of the acid chloride.

Answer 8

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Answer 9

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Answer 10

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Answer 11

Ch. 16.1 - The aromas of many flowers and fruits are due to...Ch. 16.1 - Prob. 2P Ch. 16.1 - Name the following:Ch. 16.1 - Prob. 4P Ch. 16.2 - Prob. 5P Ch. 16.2 - Which is longer, the carbon-oxygen single bond in...Ch. 16.2 - There are three carbon-oxygen bonds in methyl...Ch. 16.2 - Prob. 8P Ch. 16.4 - Prob. 9P Ch. 16.4 - Prob. 10P

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