The enolate that is formed when the given ketone reacts with LDA has to be drawn. Concept Introduction: The structure of LDA : The name L D A stands for L i t h i u m d i i s o p r o p y l a m i d e . Since LDA is being a bulky base, it always prefers to attack only the less hindered site α- Carbon atom of ketone and forms the enolate which will be resonance stabilized. Enolate formation: When ketones are treated with a strong base, the α-position of the ketone will be deprotonated to give a resonance-stabilized intermediate called an enolate . Example:

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Answer 1

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Definition Definition Organic compounds that have a carbonyl group, C = O, as their functional group. The carbonyl group in ketones is placed somewhere in the middle of the molecular structure, which means, the C=O is attached to two alkyl groups or benzene rings. Just like all other homologous series, the naming of ketones is done using a common suffix “-one”. The general molecular formula is C n H 2n O. Functional group of a ketone

Chapter 21, Problem 53PP

(a)

Interpretation Introduction

Interpretation:

The enolate that is formed when the given ketone reacts with LDA has to be drawn.

Concept Introduction:

The structure of LDA :

The name LDA stands for Lithium diisopropyl amide.

Since LDA is being a bulky base, it always prefers to attack only the less hindered site α- Carbon atom of ketone and forms the enolate which will be resonance stabilized.

Enolate formation:

When ketones are treated with a strong base, the α-position of the ketone will be deprotonated to give a resonance-stabilized intermediate called an enolate.

Example:

(b)

Interpretation Introduction

Interpretation:

The enolate that is formed when the given ketone reacts with LDA has to be drawn.

Concept Introduction:

The structure of LDA :

The name LDA stands for Lithium diisopropyl amide.

Since LDA is being a bulky base, it always prefers to attack only the less hindered site α- Carbon atom of ketone and forms the enolate which will be resonance stabilized.

Enolate formation:

When ketones are treated with a strong base, the α-position of the ketone will be deprotonated to give a resonance-stabilized intermediate called an enolate.

Example:

(c)

Interpretation Introduction

Interpretation:

The enolate that is formed when the given ketone reacts with has to be drawn.

Concept Introduction:

The structure of LDA :

The name LDA stands for Lithium diisopropyl amide.

Since LDA is being a bulky base, it always prefers to attack only the less hindered site α- Carbon atom of ketone and forms the enolate which will be resonance stabilized.

Enolate formation:

When ketones are treated with a strong base, the α-position of the ketone will be deprotonated to give a resonance-stabilized intermediate called an enolate.

Example:

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Answer 2

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Definition Definition Organic compounds that have a carbonyl group, C = O, as their functional group. The carbonyl group in ketones is placed somewhere in the middle of the molecular structure, which means, the C=O is attached to two alkyl groups or benzene rings. Just like all other homologous series, the naming of ketones is done using a common suffix “-one”. The general molecular formula is C n H 2n O. Functional group of a ketone

Chapter 21, Problem 53PP

(a)

Interpretation Introduction

Interpretation:

The enolate that is formed when the given ketone reacts with LDA has to be drawn.

Concept Introduction:

The structure of LDA :

The name LDA stands for Lithium diisopropyl amide.

Since LDA is being a bulky base, it always prefers to attack only the less hindered site α- Carbon atom of ketone and forms the enolate which will be resonance stabilized.

Enolate formation:

When ketones are treated with a strong base, the α-position of the ketone will be deprotonated to give a resonance-stabilized intermediate called an enolate.

Example:

(b)

Interpretation Introduction

Interpretation:

The enolate that is formed when the given ketone reacts with LDA has to be drawn.

Concept Introduction:

The structure of LDA :

The name LDA stands for Lithium diisopropyl amide.

Since LDA is being a bulky base, it always prefers to attack only the less hindered site α- Carbon atom of ketone and forms the enolate which will be resonance stabilized.

Enolate formation:

When ketones are treated with a strong base, the α-position of the ketone will be deprotonated to give a resonance-stabilized intermediate called an enolate.

Example:

(c)

Interpretation Introduction

Interpretation:

The enolate that is formed when the given ketone reacts with has to be drawn.

Concept Introduction:

The structure of LDA :

The name LDA stands for Lithium diisopropyl amide.

Since LDA is being a bulky base, it always prefers to attack only the less hindered site α- Carbon atom of ketone and forms the enolate which will be resonance stabilized.

Enolate formation:

When ketones are treated with a strong base, the α-position of the ketone will be deprotonated to give a resonance-stabilized intermediate called an enolate.

Example:

Expert Solution & Answer

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Check out a sample textbook solution

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Answer 3

Question

Definition Definition Organic compounds that have a carbonyl group, C = O, as their functional group. The carbonyl group in ketones is placed somewhere in the middle of the molecular structure, which means, the C=O is attached to two alkyl groups or benzene rings. Just like all other homologous series, the naming of ketones is done using a common suffix “-one”. The general molecular formula is C n H 2n O. Functional group of a ketone

Chapter 21, Problem 53PP

(a)

Interpretation Introduction

Interpretation:

The enolate that is formed when the given ketone reacts with LDA has to be drawn.

Concept Introduction:

The structure of LDA :

The name LDA stands for Lithium diisopropyl amide.

Since LDA is being a bulky base, it always prefers to attack only the less hindered site α- Carbon atom of ketone and forms the enolate which will be resonance stabilized.

Enolate formation:

When ketones are treated with a strong base, the α-position of the ketone will be deprotonated to give a resonance-stabilized intermediate called an enolate.

Example:

(b)

Interpretation Introduction

Interpretation:

The enolate that is formed when the given ketone reacts with LDA has to be drawn.

Concept Introduction:

The structure of LDA :

The name LDA stands for Lithium diisopropyl amide.

Since LDA is being a bulky base, it always prefers to attack only the less hindered site α- Carbon atom of ketone and forms the enolate which will be resonance stabilized.

Enolate formation:

When ketones are treated with a strong base, the α-position of the ketone will be deprotonated to give a resonance-stabilized intermediate called an enolate.

Example:

(c)

Interpretation Introduction

Interpretation:

The enolate that is formed when the given ketone reacts with has to be drawn.

Concept Introduction:

The structure of LDA :

The name LDA stands for Lithium diisopropyl amide.

Since LDA is being a bulky base, it always prefers to attack only the less hindered site α- Carbon atom of ketone and forms the enolate which will be resonance stabilized.

Enolate formation:

When ketones are treated with a strong base, the α-position of the ketone will be deprotonated to give a resonance-stabilized intermediate called an enolate.

Example:

Expert Solution & Answer

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Answer 4

Question

Definition Definition Organic compounds that have a carbonyl group, C = O, as their functional group. The carbonyl group in ketones is placed somewhere in the middle of the molecular structure, which means, the C=O is attached to two alkyl groups or benzene rings. Just like all other homologous series, the naming of ketones is done using a common suffix “-one”. The general molecular formula is C n H 2n O. Functional group of a ketone

Chapter 21, Problem 53PP

(a)

Interpretation Introduction

Interpretation:

The enolate that is formed when the given ketone reacts with LDA has to be drawn.

Concept Introduction:

The structure of LDA :

The name LDA stands for Lithium diisopropyl amide.

Since LDA is being a bulky base, it always prefers to attack only the less hindered site α- Carbon atom of ketone and forms the enolate which will be resonance stabilized.

Enolate formation:

When ketones are treated with a strong base, the α-position of the ketone will be deprotonated to give a resonance-stabilized intermediate called an enolate.

Example:

(b)

Interpretation Introduction

Interpretation:

The enolate that is formed when the given ketone reacts with LDA has to be drawn.

Concept Introduction:

The structure of LDA :

The name LDA stands for Lithium diisopropyl amide.

Since LDA is being a bulky base, it always prefers to attack only the less hindered site α- Carbon atom of ketone and forms the enolate which will be resonance stabilized.

Enolate formation:

When ketones are treated with a strong base, the α-position of the ketone will be deprotonated to give a resonance-stabilized intermediate called an enolate.

Example:

(c)

Interpretation Introduction

Interpretation:

The enolate that is formed when the given ketone reacts with has to be drawn.

Concept Introduction:

The structure of LDA :

The name LDA stands for Lithium diisopropyl amide.

Since LDA is being a bulky base, it always prefers to attack only the less hindered site α- Carbon atom of ketone and forms the enolate which will be resonance stabilized.

Enolate formation:

When ketones are treated with a strong base, the α-position of the ketone will be deprotonated to give a resonance-stabilized intermediate called an enolate.

Example:

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Answer 5

Chapter 21, Problem 53PP

(a)

Interpretation Introduction

Interpretation:

The enolate that is formed when the given ketone reacts with LDA has to be drawn.

Concept Introduction:

The structure of LDA :

The name LDA stands for Lithium diisopropyl amide.

Since LDA is being a bulky base, it always prefers to attack only the less hindered site α- Carbon atom of ketone and forms the enolate which will be resonance stabilized.

Enolate formation:

When ketones are treated with a strong base, the α-position of the ketone will be deprotonated to give a resonance-stabilized intermediate called an enolate.

Example:

(b)

Interpretation Introduction

Interpretation:

The enolate that is formed when the given ketone reacts with LDA has to be drawn.

Concept Introduction:

The structure of LDA :

The name LDA stands for Lithium diisopropyl amide.

Since LDA is being a bulky base, it always prefers to attack only the less hindered site α- Carbon atom of ketone and forms the enolate which will be resonance stabilized.

Enolate formation:

When ketones are treated with a strong base, the α-position of the ketone will be deprotonated to give a resonance-stabilized intermediate called an enolate.

Example:

(c)

Interpretation Introduction

Interpretation:

The enolate that is formed when the given ketone reacts with has to be drawn.

Concept Introduction:

The structure of LDA :

The name LDA stands for Lithium diisopropyl amide.

Since LDA is being a bulky base, it always prefers to attack only the less hindered site α- Carbon atom of ketone and forms the enolate which will be resonance stabilized.

Enolate formation:

When ketones are treated with a strong base, the α-position of the ketone will be deprotonated to give a resonance-stabilized intermediate called an enolate.

Example:

Answer 6

Chapter 21, Problem 53PP

(a)

Interpretation Introduction

Interpretation:

The enolate that is formed when the given ketone reacts with LDA has to be drawn.

Concept Introduction:

The structure of LDA :

The name LDA stands for Lithium diisopropyl amide.

Since LDA is being a bulky base, it always prefers to attack only the less hindered site α- Carbon atom of ketone and forms the enolate which will be resonance stabilized.

Enolate formation:

When ketones are treated with a strong base, the α-position of the ketone will be deprotonated to give a resonance-stabilized intermediate called an enolate.

Example:

Answer 7

Chapter 21, Problem 53PP

(a)

Interpretation Introduction

Interpretation:

The enolate that is formed when the given ketone reacts with LDA has to be drawn.

Concept Introduction:

The structure of LDA :

The name LDA stands for Lithium diisopropyl amide.

Since LDA is being a bulky base, it always prefers to attack only the less hindered site α- Carbon atom of ketone and forms the enolate which will be resonance stabilized.

Enolate formation:

When ketones are treated with a strong base, the α-position of the ketone will be deprotonated to give a resonance-stabilized intermediate called an enolate.

Example:

Answer 8

(b)

Interpretation Introduction

Interpretation:

The enolate that is formed when the given ketone reacts with LDA has to be drawn.

Concept Introduction:

The structure of LDA :

The name LDA stands for Lithium diisopropyl amide.

Since LDA is being a bulky base, it always prefers to attack only the less hindered site α- Carbon atom of ketone and forms the enolate which will be resonance stabilized.

Enolate formation:

When ketones are treated with a strong base, the α-position of the ketone will be deprotonated to give a resonance-stabilized intermediate called an enolate.

Example:

Answer 9

(b)

Interpretation Introduction

Interpretation:

The enolate that is formed when the given ketone reacts with LDA has to be drawn.

Concept Introduction:

The structure of LDA :

The name LDA stands for Lithium diisopropyl amide.

Since LDA is being a bulky base, it always prefers to attack only the less hindered site α- Carbon atom of ketone and forms the enolate which will be resonance stabilized.

Enolate formation:

When ketones are treated with a strong base, the α-position of the ketone will be deprotonated to give a resonance-stabilized intermediate called an enolate.

Example:

Answer 10

(c)

Interpretation Introduction

Interpretation:

The enolate that is formed when the given ketone reacts with has to be drawn.

Concept Introduction:

The structure of LDA :

The name LDA stands for Lithium diisopropyl amide.

Since LDA is being a bulky base, it always prefers to attack only the less hindered site α- Carbon atom of ketone and forms the enolate which will be resonance stabilized.

Enolate formation:

When ketones are treated with a strong base, the α-position of the ketone will be deprotonated to give a resonance-stabilized intermediate called an enolate.

Example:

Answer 11

(c)

Interpretation Introduction

Interpretation:

The enolate that is formed when the given ketone reacts with has to be drawn.

Concept Introduction:

The structure of LDA :

The name LDA stands for Lithium diisopropyl amide.

Since LDA is being a bulky base, it always prefers to attack only the less hindered site α- Carbon atom of ketone and forms the enolate which will be resonance stabilized.

Enolate formation:

When ketones are treated with a strong base, the α-position of the ketone will be deprotonated to give a resonance-stabilized intermediate called an enolate.

Example:

Answer 12

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Answer 15

Ch. 21.1 - Prob. 1CC Ch. 21.1 - Prob. 2CC Ch. 21.1 - Prob. 3CC Ch. 21.1 - Prob. 1LTS Ch. 21.1 - Prob. 4PTS Ch. 21.1 - APPLY the skill As with aldehydes and ketones, the...Ch. 21.1 - Draw the enolate ion that is formed when each of...Ch. 21.1 - Prob. 7CC Ch. 21.2 - Prob. 8CC Ch. 21.2 - Prob. 9CC

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