The mechanism of intramolecular aldol reaction involving heptanedial is to be drawn, along with the major product. Why this reaction is favored is to explained. Concept introduction: Intramolecular reactions are the ones in which the electron-rich and electron-poor sites are present within the same molecule. When ketones or aldehydes are treated with a strong base, they yield β -hydroxycarbonyl compounds via an aldol addition. Under these basic conditions, an enolate anion acts as a nucleophile. An intramolecular reaction is favored when it forms a five or six-membered ring. Intramolecular reactions involving the attack of an aldehyde C=O are favored over ones involving the attack of a ketone C=O . The first step is the formation of an enolate ion. The HO − reversibly deprotonates the alpha carbon to yield an enolate anion. In step two, the newly formed enolate anion, which serves as a nucleophile, attacks the carbonyl carbon present within the same molecule. The product of this step is an alkoxide ion, which is subsequently protonated in step 3.

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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 18, Problem 18.31P

Interpretation Introduction

Interpretation:

The mechanism of intramolecular aldol reaction involving heptanedial is to be drawn, along with the major product. Why this reaction is favored is to explained.

Concept introduction:

Intramolecular reactions are the ones in which the electron-rich and electron-poor sites are present within the same molecule. When ketones or aldehydes are treated with a strong base, they yield β-hydroxycarbonyl compounds via an aldol addition. Under these basic conditions, an enolate anion acts as a nucleophile. An intramolecular reaction is favored when it forms a five or six-membered ring. Intramolecular reactions involving the attack of an aldehyde C=O are favored over ones involving the attack of a ketone C=O.

The first step is the formation of an enolate ion. The HO− reversibly deprotonates the alpha carbon to yield an enolate anion. In step two, the newly formed enolate anion, which serves as a nucleophile, attacks the carbonyl carbon present within the same molecule. The product of this step is an alkoxide ion, which is subsequently protonated in step 3.

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Why doesn't this carry on to form a ring by deprotonating the alpha carbon and the negatively-charged carbon attacking the C=O?

6. A solution (0.0004 M) of Fe(S2CNEt2)3 (see the structural drawing below) in chloroform has absorption bands at: 350 nm (absorbance A = 2.34); 514 nm(absorbance A = 0.0532); Calculate the molar absorptivity values for these bands. Comment on their possible nature (charge transfer transitions or d-d S N- transitions?). (4 points)

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 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 18, Problem 18.31P

Interpretation Introduction

Interpretation:

The mechanism of intramolecular aldol reaction involving heptanedial is to be drawn, along with the major product. Why this reaction is favored is to explained.

Concept introduction:

Intramolecular reactions are the ones in which the electron-rich and electron-poor sites are present within the same molecule. When ketones or aldehydes are treated with a strong base, they yield β-hydroxycarbonyl compounds via an aldol addition. Under these basic conditions, an enolate anion acts as a nucleophile. An intramolecular reaction is favored when it forms a five or six-membered ring. Intramolecular reactions involving the attack of an aldehyde C=O are favored over ones involving the attack of a ketone C=O.

The first step is the formation of an enolate ion. The HO− reversibly deprotonates the alpha carbon to yield an enolate anion. In step two, the newly formed enolate anion, which serves as a nucleophile, attacks the carbonyl carbon present within the same molecule. The product of this step is an alkoxide ion, which is subsequently protonated in step 3.

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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 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 18, Problem 18.31P

Interpretation Introduction

Interpretation:

The mechanism of intramolecular aldol reaction involving heptanedial is to be drawn, along with the major product. Why this reaction is favored is to explained.

Concept introduction:

Intramolecular reactions are the ones in which the electron-rich and electron-poor sites are present within the same molecule. When ketones or aldehydes are treated with a strong base, they yield β-hydroxycarbonyl compounds via an aldol addition. Under these basic conditions, an enolate anion acts as a nucleophile. An intramolecular reaction is favored when it forms a five or six-membered ring. Intramolecular reactions involving the attack of an aldehyde C=O are favored over ones involving the attack of a ketone C=O.

The first step is the formation of an enolate ion. The HO− reversibly deprotonates the alpha carbon to yield an enolate anion. In step two, the newly formed enolate anion, which serves as a nucleophile, attacks the carbonyl carbon present within the same molecule. The product of this step is an alkoxide ion, which is subsequently protonated in step 3.

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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 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 18, Problem 18.31P

Interpretation Introduction