Starting from materials having five or fewer carbons how 3-methyl-2-hexenoic acid (mixture of E and Z isomers) can be synthesized is to be shown. Concept introduction: The following steps are involved in the synthesis of 3-methyl-2-hexenoic acid (mixture of E and Z isomers) from materials having five carbons i) Nucleophilic addition of a Grignard reagent (with an unsaturated carbon chain) to the carbonyl carbon in a methyl ketone to get an unsaturated alcohol ii) Addition of water to the double bond through hydroboration followed by oxidation to yield a diol . iii) Oxidation of the alcohol to acid iv) dehydration of the acid to get the unsaturated acid. To show: Starting from materials having five or fewer carbons how 3-methyl-2-hexenoic acid (mixture of E and Z isomers) can be synthesized.

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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 20.SE, Problem 52AP

Interpretation Introduction

Interpretation:

Starting from materials having five or fewer carbons how 3-methyl-2-hexenoic acid (mixture of E and Z isomers) can be synthesized is to be shown.

Concept introduction:

The following steps are involved in the synthesis of 3-methyl-2-hexenoic acid (mixture of E and Z isomers) from materials having five carbons i) Nucleophilic addition of a Grignard reagent (with an unsaturated carbon chain) to the carbonyl carbon in a methyl ketone to get an unsaturated alcohol ii) Addition of water to the double bond through hydroboration followed by oxidation to yield a diol. iii) Oxidation of the alcohol to acid iv) dehydration of the acid to get the unsaturated acid.

To show:

Starting from materials having five or fewer carbons how 3-methyl-2-hexenoic acid (mixture of E and Z isomers) can be synthesized.

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a. •Write all of the possible products For the Following ronction А ----- H - H H + H₂0 H+ Н b. in Rite the complete reaction Mechaniszn For the Formation of each product. ·C. Suggest what Reaction conditions could Result in each product being the major Product of the veaction:

a. Write the product For each of the Following reactions H 6-836-6 레 +H₂ N A H A-C-C=C-C-CH + 2 Na +2 NH3 - H H b. Write the reaction Mechanism For. reaction each

help draw the molecule

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 20.SE, Problem 52AP

Interpretation Introduction

Interpretation:

Starting from materials having five or fewer carbons how 3-methyl-2-hexenoic acid (mixture of E and Z isomers) can be synthesized is to be shown.

Concept introduction:

The following steps are involved in the synthesis of 3-methyl-2-hexenoic acid (mixture of E and Z isomers) from materials having five carbons i) Nucleophilic addition of a Grignard reagent (with an unsaturated carbon chain) to the carbonyl carbon in a methyl ketone to get an unsaturated alcohol ii) Addition of water to the double bond through hydroboration followed by oxidation to yield a diol. iii) Oxidation of the alcohol to acid iv) dehydration of the acid to get the unsaturated acid.

To show:

Starting from materials having five or fewer carbons how 3-methyl-2-hexenoic acid (mixture of E and Z isomers) can be synthesized.

Expert Solution & Answer

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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 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 20.SE, Problem 52AP

Interpretation Introduction

Interpretation:

Starting from materials having five or fewer carbons how 3-methyl-2-hexenoic acid (mixture of E and Z isomers) can be synthesized is to be shown.

Concept introduction:

The following steps are involved in the synthesis of 3-methyl-2-hexenoic acid (mixture of E and Z isomers) from materials having five carbons i) Nucleophilic addition of a Grignard reagent (with an unsaturated carbon chain) to the carbonyl carbon in a methyl ketone to get an unsaturated alcohol ii) Addition of water to the double bond through hydroboration followed by oxidation to yield a diol. iii) Oxidation of the alcohol to acid iv) dehydration of the acid to get the unsaturated acid.

To show:

Starting from materials having five or fewer carbons how 3-methyl-2-hexenoic acid (mixture of E and Z isomers) can be synthesized.

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 20.SE, Problem 52AP

Interpretation Introduction