(a) Interpretation: The complete, detailed mechanism for the given reaction is to be drawn and the major product of the given reaction is to be determined. Concept introduction: Enamines are inherently less reactive than their enolate ion analogs, it is necessary to treat them with highly reactive alkylating agents in order to effect a reaction. Enamines are not as nucleophilic as their enolate ion equivalents.

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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 18, Problem 18.82P

Interpretation Introduction

(a)

Interpretation:

The complete, detailed mechanism for the given reaction is to be drawn and the major product of the given reaction is to be determined.

Concept introduction:

Enamines are inherently less reactive than their enolate ion analogs, it is necessary to treat them with highly reactive alkylating agents in order to effect a reaction. Enamines are not as nucleophilic as their enolate ion equivalents.

Interpretation Introduction

(b)

Interpretation:

The complete, detailed mechanism for the given reaction is to be drawn and the major product of the given reaction is to be determined.

Concept introduction:

Enamines are inherently less reactive than their enolate ion analogs, it is necessary to treat them with highly reactive alkylating agents in order to effect a reaction. Enamines are not as nucleophilic as their enolate ion equivalents.

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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]

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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 18, Problem 18.82P

Interpretation Introduction

(a)

Interpretation:

The complete, detailed mechanism for the given reaction is to be drawn and the major product of the given reaction is to be determined.

Concept introduction:

Enamines are inherently less reactive than their enolate ion analogs, it is necessary to treat them with highly reactive alkylating agents in order to effect a reaction. Enamines are not as nucleophilic as their enolate ion equivalents.

Interpretation Introduction

(b)

Interpretation:

The complete, detailed mechanism for the given reaction is to be drawn and the major product of the given reaction is to be determined.

Concept introduction:

Enamines are inherently less reactive than their enolate ion analogs, it is necessary to treat them with highly reactive alkylating agents in order to effect a reaction. Enamines are not as nucleophilic as their enolate ion equivalents.

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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 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 18, Problem 18.82P

Interpretation Introduction

(a)

Interpretation:

The complete, detailed mechanism for the given reaction is to be drawn and the major product of the given reaction is to be determined.

Concept introduction:

Enamines are inherently less reactive than their enolate ion analogs, it is necessary to treat them with highly reactive alkylating agents in order to effect a reaction. Enamines are not as nucleophilic as their enolate ion equivalents.

Interpretation Introduction

(b)

Interpretation:

The complete, detailed mechanism for the given reaction is to be drawn and the major product of the given reaction is to be determined.

Concept introduction:

Enamines are inherently less reactive than their enolate ion analogs, it is necessary to treat them with highly reactive alkylating agents in order to effect a reaction. Enamines are not as nucleophilic as their enolate ion equivalents.

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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 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 18, Problem 18.82P

Interpretation Introduction

(a)

Interpretation:

The complete, detailed mechanism for the given reaction is to be drawn and the major product of the given reaction is to be determined.

Concept introduction:

Enamines are inherently less reactive than their enolate ion analogs, it is necessary to treat them with highly reactive alkylating agents in order to effect a reaction. Enamines are not as nucleophilic as their enolate ion equivalents.

Interpretation Introduction

(b)

Interpretation:

The complete, detailed mechanism for the given reaction is to be drawn and the major product of the given reaction is to be determined.

Concept introduction:

Enamines are inherently less reactive than their enolate ion analogs, it is necessary to treat them with highly reactive alkylating agents in order to effect a reaction. Enamines are not as nucleophilic as their enolate ion equivalents.

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Answer 5

Chapter 18, Problem 18.82P

Interpretation Introduction

(a)

Interpretation:

The complete, detailed mechanism for the given reaction is to be drawn and the major product of the given reaction is to be determined.

Concept introduction:

Enamines are inherently less reactive than their enolate ion analogs, it is necessary to treat them with highly reactive alkylating agents in order to effect a reaction. Enamines are not as nucleophilic as their enolate ion equivalents.

Interpretation Introduction

(b)

Interpretation:

The complete, detailed mechanism for the given reaction is to be drawn and the major product of the given reaction is to be determined.

Concept introduction:

Enamines are inherently less reactive than their enolate ion analogs, it is necessary to treat them with highly reactive alkylating agents in order to effect a reaction. Enamines are not as nucleophilic as their enolate ion equivalents.

Answer 6

Chapter 18, Problem 18.82P

Interpretation Introduction

(a)

Interpretation:

The complete, detailed mechanism for the given reaction is to be drawn and the major product of the given reaction is to be determined.

Concept introduction:

Enamines are inherently less reactive than their enolate ion analogs, it is necessary to treat them with highly reactive alkylating agents in order to effect a reaction. Enamines are not as nucleophilic as their enolate ion equivalents.

Answer 7

Chapter 18, Problem 18.82P

Interpretation Introduction

(a)

Interpretation:

The complete, detailed mechanism for the given reaction is to be drawn and the major product of the given reaction is to be determined.

Concept introduction:

Enamines are inherently less reactive than their enolate ion analogs, it is necessary to treat them with highly reactive alkylating agents in order to effect a reaction. Enamines are not as nucleophilic as their enolate ion equivalents.

Answer 8

Interpretation Introduction

(b)

Interpretation:

The complete, detailed mechanism for the given reaction is to be drawn and the major product of the given reaction is to be determined.

Concept introduction:

Enamines are inherently less reactive than their enolate ion analogs, it is necessary to treat them with highly reactive alkylating agents in order to effect a reaction. Enamines are not as nucleophilic as their enolate ion equivalents.

Answer 9

Interpretation Introduction

(b)

Interpretation:

The complete, detailed mechanism for the given reaction is to be drawn and the major product of the given reaction is to be determined.

Concept introduction:

Enamines are inherently less reactive than their enolate ion analogs, it is necessary to treat them with highly reactive alkylating agents in order to effect a reaction. Enamines are not as nucleophilic as their enolate ion equivalents.

Answer 10

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Answer 11

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Answer 12

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Answer 13

Ch. 18 - Prob. 18.1P Ch. 18 - Prob. 18.2P Ch. 18 - Prob. 18.3P Ch. 18 - Prob. 18.4P Ch. 18 - Prob. 18.5P Ch. 18 - Prob. 18.6P Ch. 18 - Prob. 18.7P Ch. 18 - Prob. 18.8P Ch. 18 - Prob. 18.9P Ch. 18 - Prob. 18.10P

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