The given compound A is to be identified and mechanism of conversion of A to product is to be shown. Concept Introduction: The nucleophilic addition of aldehyde and alkoxy amine results in the formation of aldoxime. Aldoxime under basic condition rearranges to form the nitrile compound. The base abstracts the hydrogen atom from the aldoxime. Then carbon and nitrogen triple bond will be formed.

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, Problem 21.59AP

Interpretation Introduction

Interpretation:

The given compound A is to be identified and mechanism of conversion of A to product is to be shown.

Concept Introduction:

The nucleophilic addition of aldehyde and alkoxy amine results in the formation of aldoxime. Aldoxime under basic condition rearranges to form the nitrile compound. The base abstracts the hydrogen atom from the aldoxime. Then carbon and nitrogen triple bond will be formed.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

(b) Suggest a reasonable biosynthesis for the naturally occurring alkaloid coniine (isolated from hemlock), starting from octanoic acid. Coniine

If you were ask to prepare ethylamine, suggest two ways which you would give that would give you exclusively the desired product. Explain what is happening in each reaction steps.

Each of the following reactions has been carried out under conditions such that disubstitution or trisubstitution occurred. Identify the principal organic product in each case. (a) Nitration of p-chlorobenzoic acid (dinitration) (b) Bromination of aniline (tribromination) (c) Bromination of o-aminoacetophenone (dibromination) (d) Bromination of p-nitrophenol (dibromination) (e) Reaction of biphenyl with tert-butyl chloride and iron(III) chloride (dialkylation) (f) Sulfonation of phenol (disulfonation)

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, Problem 21.59AP

Interpretation Introduction

Interpretation:

The given compound A is to be identified and mechanism of conversion of A to product is to be shown.

Concept Introduction:

The nucleophilic addition of aldehyde and alkoxy amine results in the formation of aldoxime. Aldoxime under basic condition rearranges to form the nitrile compound. The base abstracts the hydrogen atom from the aldoxime. Then carbon and nitrogen triple bond will be formed.

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, Problem 21.59AP

Interpretation Introduction

Interpretation:

The given compound A is to be identified and mechanism of conversion of A to product is to be shown.

Concept Introduction:

The nucleophilic addition of aldehyde and alkoxy amine results in the formation of aldoxime. Aldoxime under basic condition rearranges to form the nitrile compound. The base abstracts the hydrogen atom from the aldoxime. Then carbon and nitrogen triple bond will be formed.

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, Problem 21.59AP

Interpretation Introduction