The carbonyl compound and enolate, in the synthesis of chalconeare to be identified by considering the retrosynthetic analysis and the equation for the complete synthesis of chalcone is to be proposed. Concept Introduction: > The reaction that the addition of an alpha carbon of an enolizable aldehyde or ketone to the carbonyl group of the another aldehyde or ketone group takes place to form β-hydroxy carbonyl compounds, such reaction is called as the aldol reaction. > Retrosynthesis is used to identify the reactants. It involves the breaking of the target molecule into starting materials.

Question

Want to see the full answer?

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 21.4, Problem 13P

Interpretation Introduction

Interpretation:

The carbonyl compound and enolate, in the synthesis of chalconeare to be identified by considering the retrosynthetic analysis and the equation for the complete synthesis of chalcone is to be proposed.

Concept Introduction:
>
The reaction that the addition of an alpha carbon of an enolizable aldehyde or ketone to the carbonyl group of the another aldehyde or ketone group takes place to form β-hydroxy carbonyl compounds, such reaction is called as the aldol reaction.
>
Retrosynthesis is used to identify the reactants. It involves the breaking of the target molecule into starting materials.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

Carboxylic acid X is an intermediate in the multistep synthesis ofproparacaine, a local anesthetic. Devise a synthesis of X from phenoland any needed organic or inorganic reagents.

Problem 17.21: Show how you could carry out the synthesis below beginning with benzaldehyde, and usmg eny other reagents necessary.

Muscalure, the sex pheromone of the common housey, can be prepared by a reaction sequence that uses two nucleophilic substitutions. Identify compounds A–D in the following synthesis of muscalure.

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 21.4, Problem 13P

Interpretation Introduction

Interpretation:

The carbonyl compound and enolate, in the synthesis of chalconeare to be identified by considering the retrosynthetic analysis and the equation for the complete synthesis of chalcone is to be proposed.

Concept Introduction:
>
The reaction that the addition of an alpha carbon of an enolizable aldehyde or ketone to the carbonyl group of the another aldehyde or ketone group takes place to form β-hydroxy carbonyl compounds, such reaction is called as the aldol reaction.
>
Retrosynthesis is used to identify the reactants. It involves the breaking of the target molecule into starting materials.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

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 21.4, Problem 13P

Interpretation Introduction

Interpretation:

The carbonyl compound and enolate, in the synthesis of chalconeare to be identified by considering the retrosynthetic analysis and the equation for the complete synthesis of chalcone is to be proposed.

Concept Introduction:
>
The reaction that the addition of an alpha carbon of an enolizable aldehyde or ketone to the carbonyl group of the another aldehyde or ketone group takes place to form β-hydroxy carbonyl compounds, such reaction is called as the aldol reaction.
>
Retrosynthesis is used to identify the reactants. It involves the breaking of the target molecule into starting materials.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

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 21.4, Problem 13P

Interpretation Introduction