The principal organic product of each of the given reactions of ammonia and amines with α, β- unsaturated carbonyl compounds is to be predicted. Concept introduction: The α, β- unsaturated carbonyl compound has double bond at α, β position with respect to the carbonyl group. In conjugate addition of carbonyl compound, the nucleophile attacks the β carbon of C=C by forming enolate ion intermediate, which is then converted to ketone in the reaction condition and gives the β substituted product.

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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 22, Problem 51P

Interpretation Introduction

Interpretation:

The principal organic product of each of the given reactions of ammonia and amines with α, β- unsaturated carbonyl compounds is to be predicted.

Concept introduction:

The α, β- unsaturated carbonyl compound has double bond at α, β position with respect to the carbonyl group.

In conjugate addition of carbonyl compound, the nucleophile attacks the β carbon of C=C by forming enolate ion intermediate, which is then converted to ketone in the reaction condition and gives the β substituted product.

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Hi!! Please provide a solution that is handwritten. Ensure all figures, reaction mechanisms (with arrows and lone pairs please!!), and structures are clearly drawn to illustrate the synthesis of the product as per the standards of a third year organic chemistry course. ****the solution must include all steps, mechanisms, and intermediate structures as required. Please hand-draw the mechanisms and structures to support your explanation. Don’t give me AI-generated diagrams or text-based explanations, no wordy explanations on how to draw the structures I need help with the exact mechanism hand drawn by you!!! I am reposting this—ensure all parts of the question are straightforward and clear or please let another expert handle it thanks!!

. (11pts total) Consider the arrows pointing at three different carbon-carbon bonds in the molecule depicted below. Bond B 2°C. +2°C. < cleavage Bond A • CH3 + 26. t cleavage 2°C• +3°C• Bond C Cleavage CH3 ZC '2°C. 26. E Strongest 3°C. 2C. Gund Largest BDE weakest bond In that molecule a. (2pts) Which bond between A-C is weakest? Which is strongest? Place answers in appropriate boxes. Weakest C bond Produces A Weakest Bond Most Strongest Bond Stable radical Strongest Gund produces least stable radicals b. (4pts) Consider the relative stability of all cleavage products that form when bonds A, B, AND C are homolytically cleaved/broken. Hint: cleavage products of bonds A, B, and C are all carbon radicals. i. Which ONE cleavage product is the most stable? A condensed or bond line representation is fine. 人 8°C. formed in bound C cleavage ii. Which ONE cleavage product is the least stable? A condensed or bond line representation is fine. methyl radical •CH3 formed in bund A Cleavage

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 22, Problem 51P

Interpretation Introduction

Interpretation:

The principal organic product of each of the given reactions of ammonia and amines with α, β- unsaturated carbonyl compounds is to be predicted.

Concept introduction:

The α, β- unsaturated carbonyl compound has double bond at α, β position with respect to the carbonyl group.

In conjugate addition of carbonyl compound, the nucleophile attacks the β carbon of C=C by forming enolate ion intermediate, which is then converted to ketone in the reaction condition and gives the β substituted product.

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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 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 22, Problem 51P

Interpretation Introduction

Interpretation:

The principal organic product of each of the given reactions of ammonia and amines with α, β- unsaturated carbonyl compounds is to be predicted.

Concept introduction:

The α, β- unsaturated carbonyl compound has double bond at α, β position with respect to the carbonyl group.

In conjugate addition of carbonyl compound, the nucleophile attacks the β carbon of C=C by forming enolate ion intermediate, which is then converted to ketone in the reaction condition and gives the β substituted product.

Expert Solution & Answer

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Check out a sample textbook solution

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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 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 22, Problem 51P

Interpretation Introduction