The products formation if ethyl ( 2 − oxocyclohexane ) carboxylate reacts according to the given reaction condition is to be explained. Concept Introduction: Claisen condensation occurs between two esters or one ester and a carbonyl compound that must have an alpha hydrogen atom with them It favors the formation of a single bond between two carbon atoms in the presence of a strong base. The product formed ion the Claisen condensation is either a β-keto ester or a β-diketone .

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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 21, Problem 46P

Interpretation Introduction

Interpretation:

The products formation if ethyl(2−oxocyclohexane)carboxylate reacts according to the given reaction condition is to be explained.

Concept Introduction:

Claisen condensation occurs between two esters or one ester and a carbonyl compound that must have an alpha hydrogen atom with them

It favors the formation of a single bond between two carbon atoms in the presence of a strong base.

The product formed ion the Claisen condensation is either a β-keto ester or a β-diketone.

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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 21, Problem 46P

Interpretation Introduction

Interpretation:

The products formation if ethyl(2−oxocyclohexane)carboxylate reacts according to the given reaction condition is to be explained.

Concept Introduction:

Claisen condensation occurs between two esters or one ester and a carbonyl compound that must have an alpha hydrogen atom with them

It favors the formation of a single bond between two carbon atoms in the presence of a strong base.

The product formed ion the Claisen condensation is either a β-keto ester or a β-diketone.

Expert Solution & Answer

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Check out a sample textbook solution

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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 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 21, Problem 46P

Interpretation Introduction

Interpretation:

The products formation if ethyl(2−oxocyclohexane)carboxylate reacts according to the given reaction condition is to be explained.

Concept Introduction:

Claisen condensation occurs between two esters or one ester and a carbonyl compound that must have an alpha hydrogen atom with them

It favors the formation of a single bond between two carbon atoms in the presence of a strong base.

The product formed ion the Claisen condensation is either a β-keto ester or a β-diketone.

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 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 21, Problem 46P

Interpretation Introduction