The expected products of the given acid catalysed reaction are to be stated. Concept introduction: When aldehydes or ketones react with a primary amine , formation of a carbinolamine takes place. Then, dehydration takes place to give C = N double bond of an imine. Imine formation takes place in the presence of an acid or a base. This reaction is reversible and it is accompanied by loss of water molecule.

Question

Want to see the full answer?

Answer 1

Question

Definition Definition Organic compounds that have a carbonyl group, C=O, as their functional group. The carbonyl group in aldehydes is placed at the end of the molecular structure, which means the C=O is attached to one hydrogen atom and an alkyl group or a benzene ring. Just like all the other homologous series in organic chemistry, the naming of aldehydes uses the suffix “-al”. The general molecular formula is C n H 2n O.

Chapter 22.4, Problem 22.8P

(a)

Interpretation Introduction

Interpretation:

The expected products of the given acid catalysed reaction are to be stated.

Concept introduction:

When aldehydes or ketones react with a primary amine, formation of a carbinolamine takes place. Then, dehydration takes place to give $C=N$ double bond of an imine. Imine formation takes place in the presence of an acid or a base. This reaction is reversible and it is accompanied by loss of water molecule.

(b)

Interpretation Introduction

Interpretation:

The expected products of the given acid catalysed reaction are to be stated.

Concept introduction:

When aldehydes or ketones react with a secondary amine, formation of enamine takes place. The nitrogen analog of an enol is known as enamine. From the resonating structures of enamine, it is clear that it nucleophilic in nature.

(c)

Interpretation Introduction

Interpretation:

The expected products of the given acid catalysed reaction are to be stated.

Concept introduction:

When aldehydes or ketones react with a primary amine, formation of a carbinolamine takes place. Then, dehydration takes place to give $C=N$ double bond of an imine. Imine formation takes place in the presence of an acid or a base. This reaction is reversible and it is accompanied by loss of water molecule.

(d)

Interpretation Introduction

Interpretation:

The expected products of the given acid catalysed reaction are to be stated.

Concept introduction:

When aldehydes or ketones react with a secondary amine, formation of enamine takes place. The nitrogen analog of an enol is known as enamine. From the resonating structures of enamine, it is clear that it nucleophilic in nature.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

1/2 - 51% + » GAY Organic Reactions Assignment /26 Write the type of reaction that is occurring on the line provided then complete the reaction. Only include the major products and any byproducts (e.g. H₂O) but no minor products. Please use either full structural diagrams or the combination method shown in the lesson. Skeletal/line diagrams will not be accepted. H3C 1. 2. CH3 A Acid OH Type of Reaction: NH Type of Reaction: + H₂O Catalyst + HBr 3. Type of Reaction: H3C 4. Type Reaction: 5. H3C CH2 + H2O OH + [0] CH3 Type of Reaction: 6. OH CH3 HO CH3 + Type of Reaction: 7. Type of Reaction: + [H]

humbnai Concentration Terms[1].pdf ox + New Home Edit Sign in Comment Convert Page Fill & Sign Protect Tools Batch +WPS A Free Trial Share Inter Concreting Concentration forms. Hydrogen peroxide is a powerful oxidizing agent wed in concentrated solution in rocket fuels and in dilute solution as a hair bleach. An aqueous sulation of H2O2 is 30% by mass and has density of #liligime calculat the Ⓒmolality ⑥mole fraction of molarity. 20 9. B. A sample of Commercial Concentrated hydrochloric ET

If a reaction occurs, what would be the major products? Please include a detailed explanation as well as a drawing showing how the reaction occurs and what the final product is.

Answer 2

Question

Definition Definition Organic compounds that have a carbonyl group, C=O, as their functional group. The carbonyl group in aldehydes is placed at the end of the molecular structure, which means the C=O is attached to one hydrogen atom and an alkyl group or a benzene ring. Just like all the other homologous series in organic chemistry, the naming of aldehydes uses the suffix “-al”. The general molecular formula is C n H 2n O.

Chapter 22.4, Problem 22.8P

(a)

Interpretation Introduction

Interpretation:

The expected products of the given acid catalysed reaction are to be stated.

Concept introduction:

When aldehydes or ketones react with a primary amine, formation of a carbinolamine takes place. Then, dehydration takes place to give $C=N$ double bond of an imine. Imine formation takes place in the presence of an acid or a base. This reaction is reversible and it is accompanied by loss of water molecule.

(b)

Interpretation Introduction

Interpretation:

The expected products of the given acid catalysed reaction are to be stated.

Concept introduction:

When aldehydes or ketones react with a secondary amine, formation of enamine takes place. The nitrogen analog of an enol is known as enamine. From the resonating structures of enamine, it is clear that it nucleophilic in nature.

(c)

Interpretation Introduction

Interpretation:

The expected products of the given acid catalysed reaction are to be stated.

Concept introduction:

When aldehydes or ketones react with a primary amine, formation of a carbinolamine takes place. Then, dehydration takes place to give $C=N$ double bond of an imine. Imine formation takes place in the presence of an acid or a base. This reaction is reversible and it is accompanied by loss of water molecule.

(d)

Interpretation Introduction

Interpretation:

The expected products of the given acid catalysed reaction are to be stated.

Concept introduction:

When aldehydes or ketones react with a secondary amine, formation of enamine takes place. The nitrogen analog of an enol is known as enamine. From the resonating structures of enamine, it is clear that it nucleophilic in nature.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 3

Question

Definition Definition Organic compounds that have a carbonyl group, C=O, as their functional group. The carbonyl group in aldehydes is placed at the end of the molecular structure, which means the C=O is attached to one hydrogen atom and an alkyl group or a benzene ring. Just like all the other homologous series in organic chemistry, the naming of aldehydes uses the suffix “-al”. The general molecular formula is C n H 2n O.

Chapter 22.4, Problem 22.8P

(a)

Interpretation Introduction

Interpretation:

The expected products of the given acid catalysed reaction are to be stated.

Concept introduction:

When aldehydes or ketones react with a primary amine, formation of a carbinolamine takes place. Then, dehydration takes place to give $C=N$ double bond of an imine. Imine formation takes place in the presence of an acid or a base. This reaction is reversible and it is accompanied by loss of water molecule.

(b)

Interpretation Introduction

Interpretation:

The expected products of the given acid catalysed reaction are to be stated.

Concept introduction:

When aldehydes or ketones react with a secondary amine, formation of enamine takes place. The nitrogen analog of an enol is known as enamine. From the resonating structures of enamine, it is clear that it nucleophilic in nature.

(c)

Interpretation Introduction

Interpretation:

The expected products of the given acid catalysed reaction are to be stated.

Concept introduction:

When aldehydes or ketones react with a primary amine, formation of a carbinolamine takes place. Then, dehydration takes place to give $C=N$ double bond of an imine. Imine formation takes place in the presence of an acid or a base. This reaction is reversible and it is accompanied by loss of water molecule.

(d)

Interpretation Introduction

Interpretation:

The expected products of the given acid catalysed reaction are to be stated.

Concept introduction:

When aldehydes or ketones react with a secondary amine, formation of enamine takes place. The nitrogen analog of an enol is known as enamine. From the resonating structures of enamine, it is clear that it nucleophilic in nature.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 4

Question

Definition Definition Organic compounds that have a carbonyl group, C=O, as their functional group. The carbonyl group in aldehydes is placed at the end of the molecular structure, which means the C=O is attached to one hydrogen atom and an alkyl group or a benzene ring. Just like all the other homologous series in organic chemistry, the naming of aldehydes uses the suffix “-al”. The general molecular formula is C n H 2n O.

Chapter 22.4, Problem 22.8P

(a)

Interpretation Introduction

Interpretation:

The expected products of the given acid catalysed reaction are to be stated.

Concept introduction:

When aldehydes or ketones react with a primary amine, formation of a carbinolamine takes place. Then, dehydration takes place to give $C=N$ double bond of an imine. Imine formation takes place in the presence of an acid or a base. This reaction is reversible and it is accompanied by loss of water molecule.

(b)

Interpretation Introduction

Interpretation:

The expected products of the given acid catalysed reaction are to be stated.

Concept introduction:

When aldehydes or ketones react with a secondary amine, formation of enamine takes place. The nitrogen analog of an enol is known as enamine. From the resonating structures of enamine, it is clear that it nucleophilic in nature.

(c)

Interpretation Introduction

Interpretation:

The expected products of the given acid catalysed reaction are to be stated.

Concept introduction:

When aldehydes or ketones react with a primary amine, formation of a carbinolamine takes place. Then, dehydration takes place to give $C=N$ double bond of an imine. Imine formation takes place in the presence of an acid or a base. This reaction is reversible and it is accompanied by loss of water molecule.

(d)

Interpretation Introduction

Interpretation:

The expected products of the given acid catalysed reaction are to be stated.

Concept introduction:

When aldehydes or ketones react with a secondary amine, formation of enamine takes place. The nitrogen analog of an enol is known as enamine. From the resonating structures of enamine, it is clear that it nucleophilic in nature.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 5

Chapter 22.4, Problem 22.8P

(a)

Interpretation Introduction

Interpretation:

The expected products of the given acid catalysed reaction are to be stated.

Concept introduction:

When aldehydes or ketones react with a primary amine, formation of a carbinolamine takes place. Then, dehydration takes place to give $C=N$ double bond of an imine. Imine formation takes place in the presence of an acid or a base. This reaction is reversible and it is accompanied by loss of water molecule.

(b)

Interpretation Introduction

Interpretation:

The expected products of the given acid catalysed reaction are to be stated.

Concept introduction:

When aldehydes or ketones react with a secondary amine, formation of enamine takes place. The nitrogen analog of an enol is known as enamine. From the resonating structures of enamine, it is clear that it nucleophilic in nature.

(c)

Interpretation Introduction

Interpretation:

The expected products of the given acid catalysed reaction are to be stated.

Concept introduction:

When aldehydes or ketones react with a primary amine, formation of a carbinolamine takes place. Then, dehydration takes place to give $C=N$ double bond of an imine. Imine formation takes place in the presence of an acid or a base. This reaction is reversible and it is accompanied by loss of water molecule.

(d)

Interpretation Introduction

Interpretation:

The expected products of the given acid catalysed reaction are to be stated.

Concept introduction:

When aldehydes or ketones react with a secondary amine, formation of enamine takes place. The nitrogen analog of an enol is known as enamine. From the resonating structures of enamine, it is clear that it nucleophilic in nature.

Answer 6

Chapter 22.4, Problem 22.8P

(a)

Interpretation Introduction

Interpretation:

The expected products of the given acid catalysed reaction are to be stated.

Concept introduction:

When aldehydes or ketones react with a primary amine, formation of a carbinolamine takes place. Then, dehydration takes place to give $C=N$ double bond of an imine. Imine formation takes place in the presence of an acid or a base. This reaction is reversible and it is accompanied by loss of water molecule.

Answer 7

Chapter 22.4, Problem 22.8P

(a)

Interpretation Introduction

Interpretation:

The expected products of the given acid catalysed reaction are to be stated.

Concept introduction:

When aldehydes or ketones react with a primary amine, formation of a carbinolamine takes place. Then, dehydration takes place to give $C=N$ double bond of an imine. Imine formation takes place in the presence of an acid or a base. This reaction is reversible and it is accompanied by loss of water molecule.

Answer 8

(b)

Interpretation Introduction

Interpretation:

The expected products of the given acid catalysed reaction are to be stated.

Concept introduction:

When aldehydes or ketones react with a secondary amine, formation of enamine takes place. The nitrogen analog of an enol is known as enamine. From the resonating structures of enamine, it is clear that it nucleophilic in nature.

Answer 9

(b)

Interpretation Introduction

Interpretation:

The expected products of the given acid catalysed reaction are to be stated.

Concept introduction:

When aldehydes or ketones react with a secondary amine, formation of enamine takes place. The nitrogen analog of an enol is known as enamine. From the resonating structures of enamine, it is clear that it nucleophilic in nature.

Answer 10

(c)

Interpretation Introduction

Interpretation:

The expected products of the given acid catalysed reaction are to be stated.

Concept introduction:

When aldehydes or ketones react with a primary amine, formation of a carbinolamine takes place. Then, dehydration takes place to give $C=N$ double bond of an imine. Imine formation takes place in the presence of an acid or a base. This reaction is reversible and it is accompanied by loss of water molecule.

Answer 11

(c)

Interpretation Introduction

Interpretation:

The expected products of the given acid catalysed reaction are to be stated.

Concept introduction:

When aldehydes or ketones react with a primary amine, formation of a carbinolamine takes place. Then, dehydration takes place to give $C=N$ double bond of an imine. Imine formation takes place in the presence of an acid or a base. This reaction is reversible and it is accompanied by loss of water molecule.

Answer 12

(d)

Interpretation Introduction

Interpretation:

The expected products of the given acid catalysed reaction are to be stated.

Concept introduction:

When aldehydes or ketones react with a secondary amine, formation of enamine takes place. The nitrogen analog of an enol is known as enamine. From the resonating structures of enamine, it is clear that it nucleophilic in nature.

Answer 13

(d)

Interpretation Introduction

Interpretation:

The expected products of the given acid catalysed reaction are to be stated.

Concept introduction:

When aldehydes or ketones react with a secondary amine, formation of enamine takes place. The nitrogen analog of an enol is known as enamine. From the resonating structures of enamine, it is clear that it nucleophilic in nature.

Answer 14

Expert Solution & Answer

Answer 15

Expert Solution & Answer

Answer 16

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 17

Ch. 22.2A - Prob. 22.2P Ch. 22.4 - Without looking back, propose a mechanism for the...Ch. 22.4 - Prob. 22.8P Ch. 22.4 - Prob. 22.9P Ch. 22.5A - Prob. 22.10P Ch. 22.5A - Prob. 22.11P Ch. 22.5B - Prob. 22.12P Ch. 22.5B - Predict the products of the following reactions....Ch. 22.5B - Which compounds will give positive iodoform tests?...Ch. 22.5C - Propose a mechanism for the acid-catalyzed...

Solution Summary: The author explains the expected products of the given acid catalysed reaction.

Want to see the full answer?

Chapter 22 Solutions