The major product for the given reaction has to be predicted. Concept Introduction: Enamine formation: Aldehyde or ketone reacts with a secondary amine and forms enamine in mildly acidic conditions. Example for the formation of enamine is shown here: In enamines, the lone pair of nitrogen will be in resonance with the adjacent C=C .

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 19.6, Problem 20PTS

(a)

Interpretation Introduction

Interpretation: The major product for the given reaction has to be predicted.

Concept Introduction:

Enamine formation:

Aldehyde or ketone reacts with a secondary amine and forms enamine in mildly acidic conditions.

Example for the formation of enamine is shown here:

In enamines, the lone pair of nitrogen will be in resonance with the adjacent C=C.

(b)

Interpretation Introduction

Interpretation: The major product for the given reaction has to be predicted.

Concept Introduction:

Enamine formation:

Aldehyde or ketone reacts with a secondary amine and forms enamine in mildly acidic conditions.

Example for the formation of enamine is shown here:

In enamines, the lone pair of nitrogen will be in resonance with the adjacent C=C.

(c)

Interpretation Introduction

Interpretation: The major product for the given reaction has to be predicted.

Concept Introduction:

Aldehyde or ketone reacts with a secondary amine and forms enamine in mildly acidic conditions.

Example for the formation of enamine is shown here:

In enamines, the lone pair of nitrogen will be in resonance with the adjacent C=C.

(d)

Interpretation Introduction

Interpretation: The major product for the given reaction has to be predicted.

Concept Introduction:

Aldehyde or ketone reacts with a secondary amine and forms enamine in mildly acidic conditions.

Example for the formation of enamine is shown here:

In enamines, the lone pair of nitrogen will be in resonance with the adjacent C=C.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

What is the major product of the following reaction? O IV III HCI D = III ა IV

The reaction of what nucleophile and substrate is represented by the following transition state? CH3 CH3O -Br อ δ CH3 Methanol with 2-bromopropane Methanol with 1-bromopropane Methoxide with 1-bromopropane Methoxide with 2-bromopropane

What is the stepwise mechanism for this reaction?

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 19.6, Problem 20PTS

(a)

Interpretation Introduction

Interpretation: The major product for the given reaction has to be predicted.

Concept Introduction:

Enamine formation:

Aldehyde or ketone reacts with a secondary amine and forms enamine in mildly acidic conditions.

Example for the formation of enamine is shown here:

In enamines, the lone pair of nitrogen will be in resonance with the adjacent C=C.

(b)

Interpretation Introduction

Interpretation: The major product for the given reaction has to be predicted.

Concept Introduction:

Enamine formation:

Aldehyde or ketone reacts with a secondary amine and forms enamine in mildly acidic conditions.

Example for the formation of enamine is shown here:

In enamines, the lone pair of nitrogen will be in resonance with the adjacent C=C.

(c)

Interpretation Introduction

Interpretation: The major product for the given reaction has to be predicted.

Concept Introduction:

Aldehyde or ketone reacts with a secondary amine and forms enamine in mildly acidic conditions.

Example for the formation of enamine is shown here:

In enamines, the lone pair of nitrogen will be in resonance with the adjacent C=C.

(d)

Interpretation Introduction

Interpretation: The major product for the given reaction has to be predicted.

Concept Introduction:

Aldehyde or ketone reacts with a secondary amine and forms enamine in mildly acidic conditions.

Example for the formation of enamine is shown here:

In enamines, the lone pair of nitrogen will be in resonance with the adjacent C=C.

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 19.6, Problem 20PTS

(a)

Interpretation Introduction

Interpretation: The major product for the given reaction has to be predicted.

Concept Introduction:

Enamine formation:

Aldehyde or ketone reacts with a secondary amine and forms enamine in mildly acidic conditions.

Example for the formation of enamine is shown here:

In enamines, the lone pair of nitrogen will be in resonance with the adjacent C=C.

(b)

Interpretation Introduction

Interpretation: The major product for the given reaction has to be predicted.

Concept Introduction:

Enamine formation:

Aldehyde or ketone reacts with a secondary amine and forms enamine in mildly acidic conditions.

Example for the formation of enamine is shown here:

In enamines, the lone pair of nitrogen will be in resonance with the adjacent C=C.

(c)

Interpretation Introduction

Interpretation: The major product for the given reaction has to be predicted.

Concept Introduction:

Aldehyde or ketone reacts with a secondary amine and forms enamine in mildly acidic conditions.

Example for the formation of enamine is shown here:

In enamines, the lone pair of nitrogen will be in resonance with the adjacent C=C.

(d)

Interpretation Introduction

Interpretation: The major product for the given reaction has to be predicted.

Concept Introduction:

Aldehyde or ketone reacts with a secondary amine and forms enamine in mildly acidic conditions.

Example for the formation of enamine is shown here:

In enamines, the lone pair of nitrogen will be in resonance with the adjacent C=C.

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 19.6, Problem 20PTS

(a)

Interpretation Introduction

Interpretation: The major product for the given reaction has to be predicted.

Concept Introduction:

Enamine formation:

Aldehyde or ketone reacts with a secondary amine and forms enamine in mildly acidic conditions.

Example for the formation of enamine is shown here:

In enamines, the lone pair of nitrogen will be in resonance with the adjacent C=C.

(b)

Interpretation Introduction

Interpretation: The major product for the given reaction has to be predicted.

Concept Introduction:

Enamine formation:

Aldehyde or ketone reacts with a secondary amine and forms enamine in mildly acidic conditions.

Example for the formation of enamine is shown here:

In enamines, the lone pair of nitrogen will be in resonance with the adjacent C=C.

(c)

Interpretation Introduction

Interpretation: The major product for the given reaction has to be predicted.

Concept Introduction:

Aldehyde or ketone reacts with a secondary amine and forms enamine in mildly acidic conditions.

Example for the formation of enamine is shown here:

In enamines, the lone pair of nitrogen will be in resonance with the adjacent C=C.

(d)

Interpretation Introduction

Interpretation: The major product for the given reaction has to be predicted.

Concept Introduction:

Aldehyde or ketone reacts with a secondary amine and forms enamine in mildly acidic conditions.

Example for the formation of enamine is shown here:

In enamines, the lone pair of nitrogen will be in resonance with the adjacent C=C.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 5

Chapter 19.6, Problem 20PTS

(a)

Interpretation Introduction

Interpretation: The major product for the given reaction has to be predicted.

Concept Introduction:

Enamine formation:

Aldehyde or ketone reacts with a secondary amine and forms enamine in mildly acidic conditions.

Example for the formation of enamine is shown here:

In enamines, the lone pair of nitrogen will be in resonance with the adjacent C=C.

(b)

Interpretation Introduction

Interpretation: The major product for the given reaction has to be predicted.

Concept Introduction:

Enamine formation:

Aldehyde or ketone reacts with a secondary amine and forms enamine in mildly acidic conditions.

Example for the formation of enamine is shown here:

In enamines, the lone pair of nitrogen will be in resonance with the adjacent C=C.

(c)

Interpretation Introduction

Interpretation: The major product for the given reaction has to be predicted.

Concept Introduction:

Aldehyde or ketone reacts with a secondary amine and forms enamine in mildly acidic conditions.

Example for the formation of enamine is shown here:

In enamines, the lone pair of nitrogen will be in resonance with the adjacent C=C.

(d)

Interpretation Introduction

Interpretation: The major product for the given reaction has to be predicted.

Concept Introduction:

Aldehyde or ketone reacts with a secondary amine and forms enamine in mildly acidic conditions.

Example for the formation of enamine is shown here:

In enamines, the lone pair of nitrogen will be in resonance with the adjacent C=C.

Answer 6

Chapter 19.6, Problem 20PTS

(a)

Interpretation Introduction

Interpretation: The major product for the given reaction has to be predicted.

Concept Introduction:

Enamine formation:

Aldehyde or ketone reacts with a secondary amine and forms enamine in mildly acidic conditions.

Example for the formation of enamine is shown here:

In enamines, the lone pair of nitrogen will be in resonance with the adjacent C=C.

Answer 7

Chapter 19.6, Problem 20PTS

(a)

Interpretation Introduction

Interpretation: The major product for the given reaction has to be predicted.

Concept Introduction:

Enamine formation:

Aldehyde or ketone reacts with a secondary amine and forms enamine in mildly acidic conditions.

Example for the formation of enamine is shown here:

In enamines, the lone pair of nitrogen will be in resonance with the adjacent C=C.

Answer 8

(b)

Interpretation Introduction

Interpretation: The major product for the given reaction has to be predicted.

Concept Introduction:

Enamine formation:

Aldehyde or ketone reacts with a secondary amine and forms enamine in mildly acidic conditions.

Example for the formation of enamine is shown here:

In enamines, the lone pair of nitrogen will be in resonance with the adjacent C=C.

Answer 9

(b)

Interpretation Introduction

Interpretation: The major product for the given reaction has to be predicted.

Concept Introduction:

Enamine formation:

Aldehyde or ketone reacts with a secondary amine and forms enamine in mildly acidic conditions.

Example for the formation of enamine is shown here:

In enamines, the lone pair of nitrogen will be in resonance with the adjacent C=C.

Answer 10

(c)

Interpretation Introduction

Interpretation: The major product for the given reaction has to be predicted.

Concept Introduction:

Aldehyde or ketone reacts with a secondary amine and forms enamine in mildly acidic conditions.

Example for the formation of enamine is shown here:

In enamines, the lone pair of nitrogen will be in resonance with the adjacent C=C.

Answer 11

(c)

Interpretation Introduction

Interpretation: The major product for the given reaction has to be predicted.

Concept Introduction:

Aldehyde or ketone reacts with a secondary amine and forms enamine in mildly acidic conditions.

Example for the formation of enamine is shown here:

In enamines, the lone pair of nitrogen will be in resonance with the adjacent C=C.

Answer 12

(d)

Interpretation Introduction

Interpretation: The major product for the given reaction has to be predicted.

Concept Introduction:

Aldehyde or ketone reacts with a secondary amine and forms enamine in mildly acidic conditions.

Example for the formation of enamine is shown here:

In enamines, the lone pair of nitrogen will be in resonance with the adjacent C=C.

Answer 13

(d)

Interpretation Introduction

Interpretation: The major product for the given reaction has to be predicted.

Concept Introduction:

Aldehyde or ketone reacts with a secondary amine and forms enamine in mildly acidic conditions.

Example for the formation of enamine is shown here:

In enamines, the lone pair of nitrogen will be in resonance with the adjacent C=C.

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. 19.2 - Prob. 1LTS Ch. 19.2 - Prob. 1PTS Ch. 19.2 - Prob. 2PTS Ch. 19.2 - APPLY the skill Compounds with two ketone groups...Ch. 19.2 - Prob. 4ATS Ch. 19.3 - Prob. 5CC Ch. 19.4 - Prob. 6CC Ch. 19.5 - Prob. 7CC Ch. 19.5 - Prob. 2LTS Ch. 19.5 - Prob. 8PTS

Concept explainers

Want to see the full answer?

Chapter 19 Solutions