To explain why acetoacetic ester synthesis cannot be used to make 3,3-dimethyl-2-hexanone. Concept introduction: Acetoacetic ester synthesis is a process in which an halide is converted to a methyl ketone with two new carbon atoms (comes from acetoacetic ester). By use of this method two new alkyl groups can be introduced. A general scheme of this synthesis is shown below,

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Answer 1

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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 22.5, Problem 42ATS

Interpretation Introduction

Interpretation:

To explain why acetoacetic ester synthesis cannot be used to make 3,3-dimethyl-2-hexanone.

Concept introduction:

Acetoacetic ester synthesis is a process in which an halide is converted to a methyl ketone with two new carbon atoms (comes from acetoacetic ester). By use of this method two new alkyl groups can be introduced. A general scheme of this synthesis is shown below,

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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 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 22.5, Problem 42ATS

Interpretation Introduction

Interpretation:

To explain why acetoacetic ester synthesis cannot be used to make 3,3-dimethyl-2-hexanone.

Concept introduction:

Acetoacetic ester synthesis is a process in which an halide is converted to a methyl ketone with two new carbon atoms (comes from acetoacetic ester). By use of this method two new alkyl groups can be introduced. A general scheme of this synthesis is shown below,

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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 22.5, Problem 42ATS

Interpretation Introduction

Interpretation:

To explain why acetoacetic ester synthesis cannot be used to make 3,3-dimethyl-2-hexanone.

Concept introduction:

Acetoacetic ester synthesis is a process in which an halide is converted to a methyl ketone with two new carbon atoms (comes from acetoacetic ester). By use of this method two new alkyl groups can be introduced. A general scheme of this synthesis is shown below,

Expert Solution & Answer

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Check out a sample textbook solution

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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 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 22.5, Problem 42ATS

Interpretation Introduction