ORGANIC CHEM +SG +SAPLING >IP<
ORGANIC CHEM +SG +SAPLING >IP<
6th Edition
ISBN: 9781319171179
Author: LOUDON
Publisher: MAC HIGHER
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Chapter 26, Problem 26.10P
Interpretation Introduction

Interpretation:

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

Concept Introduction:

Erlich’s reagent is p-dimethylaminobenzaldehyde compound. It is used for the detection of pyrroles and indoles. The compound p-dimethylaminobenzaldehyde in presence of acid and ethanol reacts with pyrrole to form a colored compound. The different pyrrole and indoles are identified by the characteristic color given by them with Erlich’s reagent.

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Don't used Ai solution and don't used hand raiting
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Give the structure(s) of the product(s) the reaction below, and be sure to indicate any relative stereochemistry (you can assume that each of the Diels-Alder reactions will proceed with endo selectivity). Draw out relevant enantiomer(s) if they are expected to form. If no reaction is expected to occur under the indicated conditions, then write "no reaction" or NR, and explain why you would expect nothing to occur. If more than one product is formed, please indicate which one will be the major product or if they will be formed in equal amounts. In all cases, equimolar amounts of both components/reagents are present unless indicated otherwise   I'm struggling to see how this reaction will go! I am wondering if it will cycle on itself but I'm not sure how I drew out a decagon but I'm a bit lost
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