For Ethyl diethoxyacetate, the resonance structures have to be drawn. Concept Introduction: Enolates: 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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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 21.1, Problem 5ATS

Interpretation Introduction

Interpretation:

For Ethyl diethoxyacetate, the resonance structures have to be drawn.

Concept Introduction:

Enolates:

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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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 21.1, Problem 5ATS

Interpretation Introduction

Interpretation:

For Ethyl diethoxyacetate, the resonance structures have to be drawn.

Concept Introduction:

Enolates:

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 3

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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 21.1, Problem 5ATS

Interpretation Introduction

Interpretation:

For Ethyl diethoxyacetate, the resonance structures have to be drawn.

Concept Introduction:

Enolates:

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 4

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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 21.1, Problem 5ATS

Interpretation Introduction

Interpretation:

For Ethyl diethoxyacetate, the resonance structures have to be drawn.

Concept Introduction:

Enolates:

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 21.1, Problem 5ATS

Interpretation Introduction

Interpretation:

For Ethyl diethoxyacetate, the resonance structures have to be drawn.

Concept Introduction:

Enolates:

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 21.1, Problem 5ATS

Interpretation Introduction

Interpretation:

For Ethyl diethoxyacetate, the resonance structures have to be drawn.

Concept Introduction:

Enolates:

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 21.1, Problem 5ATS

Interpretation Introduction

Interpretation:

For Ethyl diethoxyacetate, the resonance structures have to be drawn.

Concept Introduction:

Enolates:

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 11

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

For Ethyl diethoxyacetate, the resonance structures have to be drawn. Concept Introduction: Enolates: 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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Interpretation:

For Ethyl diethoxyacetate, the resonance structures have to be drawn.

Concept Introduction:

Enolates:

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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Chapter 21 Solutions

For Ethyl diethoxyacetate, the resonance structures have to be drawn. Concept Introduction: Enolates: 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:

Concept explainers

Videos

Interpretation: For Ethyl diethoxyacetate, the resonance structures have to be drawn. Concept Introduction: Enolates: 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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Chapter 21 Solutions

Interpretation:

For Ethyl diethoxyacetate, the resonance structures have to be drawn.

Concept Introduction:

Enolates:

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: