The complete mechanism for iodination of 2, 6-dimethylcyclohexanone under basic conditions is to be drawn and the major product is to be predicted. Concept introduction: Any α hydrogens present in a carbonyl compound are weakly acidic and can be extracted by a strong base like hydroxide. This converts the electrophilic α carbon into a strongly nucleophilic species that can be used in a nucleophilic substitution reaction. As a strong nucleophile, this carbanion favors S N 2 reactions. In an S N 2 reaction, the nucleophile attacks the electrophilic carbon in the substrate, displacing the leaving group on it in a single-step, concerted reaction. Since the nucleophile attacks first, it must approach the electrophilic carbon from the direction opposite to the leaving group. This generally results in a single product with an inverted symmetry at the reaction center.

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Answer 1

Question

Chapter 10, Problem 10.12P

Interpretation Introduction

Interpretation:

The complete mechanism for iodination of 2, 6-dimethylcyclohexanone under basic conditions is to be drawn and the major product is to be predicted.

Concept introduction:

Any α hydrogens present in a carbonyl compound are weakly acidic and can be extracted by a strong base like hydroxide. This converts the electrophilic α carbon into a strongly nucleophilic species that can be used in a nucleophilic substitution reaction.

As a strong nucleophile, this carbanion favors SN2 reactions.

In an SN2 reaction, the nucleophile attacks the electrophilic carbon in the substrate, displacing the leaving group on it in a single-step, concerted reaction. Since the nucleophile attacks first, it must approach the electrophilic carbon from the direction opposite to the leaving group. This generally results in a single product with an inverted symmetry at the reaction center.

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Answer 2

Question

Chapter 10, Problem 10.12P

Interpretation Introduction

Interpretation:

The complete mechanism for iodination of 2, 6-dimethylcyclohexanone under basic conditions is to be drawn and the major product is to be predicted.

Concept introduction:

Any α hydrogens present in a carbonyl compound are weakly acidic and can be extracted by a strong base like hydroxide. This converts the electrophilic α carbon into a strongly nucleophilic species that can be used in a nucleophilic substitution reaction.

As a strong nucleophile, this carbanion favors SN2 reactions.

In an SN2 reaction, the nucleophile attacks the electrophilic carbon in the substrate, displacing the leaving group on it in a single-step, concerted reaction. Since the nucleophile attacks first, it must approach the electrophilic carbon from the direction opposite to the leaving group. This generally results in a single product with an inverted symmetry at the reaction center.

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Answer 3

Question

Chapter 10, Problem 10.12P

Interpretation Introduction

Interpretation:

The complete mechanism for iodination of 2, 6-dimethylcyclohexanone under basic conditions is to be drawn and the major product is to be predicted.

Concept introduction:

Any α hydrogens present in a carbonyl compound are weakly acidic and can be extracted by a strong base like hydroxide. This converts the electrophilic α carbon into a strongly nucleophilic species that can be used in a nucleophilic substitution reaction.

As a strong nucleophile, this carbanion favors SN2 reactions.

In an SN2 reaction, the nucleophile attacks the electrophilic carbon in the substrate, displacing the leaving group on it in a single-step, concerted reaction. Since the nucleophile attacks first, it must approach the electrophilic carbon from the direction opposite to the leaving group. This generally results in a single product with an inverted symmetry at the reaction center.

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Answer 4

Question

Chapter 10, Problem 10.12P

Interpretation Introduction

Interpretation:

The complete mechanism for iodination of 2, 6-dimethylcyclohexanone under basic conditions is to be drawn and the major product is to be predicted.

Concept introduction:

Any α hydrogens present in a carbonyl compound are weakly acidic and can be extracted by a strong base like hydroxide. This converts the electrophilic α carbon into a strongly nucleophilic species that can be used in a nucleophilic substitution reaction.

As a strong nucleophile, this carbanion favors SN2 reactions.

In an SN2 reaction, the nucleophile attacks the electrophilic carbon in the substrate, displacing the leaving group on it in a single-step, concerted reaction. Since the nucleophile attacks first, it must approach the electrophilic carbon from the direction opposite to the leaving group. This generally results in a single product with an inverted symmetry at the reaction center.

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Answer 5

Chapter 10, Problem 10.12P

Interpretation Introduction

Interpretation:

The complete mechanism for iodination of 2, 6-dimethylcyclohexanone under basic conditions is to be drawn and the major product is to be predicted.

Concept introduction:

Any α hydrogens present in a carbonyl compound are weakly acidic and can be extracted by a strong base like hydroxide. This converts the electrophilic α carbon into a strongly nucleophilic species that can be used in a nucleophilic substitution reaction.

As a strong nucleophile, this carbanion favors SN2 reactions.

In an SN2 reaction, the nucleophile attacks the electrophilic carbon in the substrate, displacing the leaving group on it in a single-step, concerted reaction. Since the nucleophile attacks first, it must approach the electrophilic carbon from the direction opposite to the leaving group. This generally results in a single product with an inverted symmetry at the reaction center.

Answer 6

Chapter 10, Problem 10.12P

Interpretation Introduction

Interpretation:

The complete mechanism for iodination of 2, 6-dimethylcyclohexanone under basic conditions is to be drawn and the major product is to be predicted.

Concept introduction:

Any α hydrogens present in a carbonyl compound are weakly acidic and can be extracted by a strong base like hydroxide. This converts the electrophilic α carbon into a strongly nucleophilic species that can be used in a nucleophilic substitution reaction.

As a strong nucleophile, this carbanion favors SN2 reactions.

In an SN2 reaction, the nucleophile attacks the electrophilic carbon in the substrate, displacing the leaving group on it in a single-step, concerted reaction. Since the nucleophile attacks first, it must approach the electrophilic carbon from the direction opposite to the leaving group. This generally results in a single product with an inverted symmetry at the reaction center.

Answer 7

Chapter 10, Problem 10.12P

Interpretation Introduction

Interpretation:

The complete mechanism for iodination of 2, 6-dimethylcyclohexanone under basic conditions is to be drawn and the major product is to be predicted.

Concept introduction:

Any α hydrogens present in a carbonyl compound are weakly acidic and can be extracted by a strong base like hydroxide. This converts the electrophilic α carbon into a strongly nucleophilic species that can be used in a nucleophilic substitution reaction.

As a strong nucleophile, this carbanion favors SN2 reactions.

In an SN2 reaction, the nucleophile attacks the electrophilic carbon in the substrate, displacing the leaving group on it in a single-step, concerted reaction. Since the nucleophile attacks first, it must approach the electrophilic carbon from the direction opposite to the leaving group. This generally results in a single product with an inverted symmetry at the reaction center.

Answer 8

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Answer 10

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Answer 11

Ch. 10 - Prob. 10.1P Ch. 10 - Prob. 10.2P Ch. 10 - Prob. 10.3P Ch. 10 - Prob. 10.4P Ch. 10 - Prob. 10.5P Ch. 10 - Prob. 10.6P Ch. 10 - Prob. 10.7P Ch. 10 - Prob. 10.8P Ch. 10 - Prob. 10.9P Ch. 10 - Prob. 10.10P

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