EBK ORGANIC CHEMISTRY
EBK ORGANIC CHEMISTRY
6th Edition
ISBN: 8220103151757
Author: LOUDON
Publisher: MAC HIGHER
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Chapter 26, Problem 26.50AP
Interpretation Introduction

(a)

Interpretation:

The curved arrow mechanism for the given reaction is to be predicted.

Concept introduction:

The addition of a bromine atom in the given compound is known as bromination. Bromination occurs through an electrophilic substitution reaction. Bromine atom acts as an electrophile which causes the formation of sigma bond in the reaction.

Interpretation Introduction

(b)

Interpretation:

The curved arrow mechanism for the given reaction is to be stated.

Concept introduction:

The consecutive aldol condensation between benzil and substituted thiodiacetate gives thiophenes as the desired product followed by nucleophilic addition reaction. This reaction is known as Hinsberg reaction.

Interpretation Introduction

(c)

Interpretation:

The curved arrow mechanism for the given reaction is to be stated.

Concept introduction:

The reaction of 2-aminobenzaldehydes with carbonyl compounds to form derivative of quinoline is known as Friedlander synthesis. The catalyst of the reaction is trifluoroacetic acid and Lewis acids.

Interpretation Introduction

(d)

Interpretation:

The curved arrow mechanism for the given reaction is to be stated.

Concept introduction:

The condensation reaction of aniline with diketones gives derivative of quinoline followed by ring closure of Schiff base intermediate. This reaction is known as Combes quinoline synthesis.

Interpretation Introduction

(e)

Interpretation:

The curved arrow mechanism for the given reaction is to be stated.

Concept introduction:

The reaction of an aldehyde with β-ketoester in the presence of NH3 undergoes condensation to form dihydropyridine as the corresponding product. This reaction is known as Hantzsch dihydropyridine synthesis.

Interpretation Introduction

(f)

Interpretation:

The curved arrow mechanism for the given reaction is to be stated.

Concept introduction:

The reaction of ortho-nitrotoulene with ethyloxalate followed by reduction with the help of Zn metal forms substituted indoles. This reaction is known as Reissert indole synthesis.

Interpretation Introduction

(g)

Interpretation:

The curved arrow mechanism for the given reaction is to be stated.

Concept introduction:

The reaction of ortho-iodoaniline with a substituted alkyne in the presence of palladium forms indoles as the corresponding product. This is a heteroannulation reaction which is known as Larsen-Chen indole synthesis.

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Part II. two unbranched ketone have molecular formulla (C8H100). El-ms showed that both of them have a molecular ion peak at m/2 =128. However ketone (A) has a fragment peak at m/2 = 99 and 72 while ketone (B) snowed a fragment peak at m/2 = 113 and 58. 9) Propose the most plausible structures for both ketones b) Explain how you arrived at your conclusion by drawing the Structures of the distinguishing fragments for each ketone, including their fragmentation mechanisms.
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