ne mechanism proceeds through a first cationic intermediate, intermediate 1. Nucleophilie attacR leads 1o mtelHmet egatively charged nucleophile, the attack of the nucleophile leads directly to the product. H. Br + CH,OH Br Intermediate 1 Intermediate 2 (product) na similar fashion, draw intermediate 1 and intermediate 2 (final product) for the following reaction. OCH3 Cl2 MEOH ČI racemic mixture • Pay attention to the reactants, they may differ from the examples. In some reactions, one part of the molecule acts as the nucleophile. • You do not have to consider stereochemistry. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate intermediate 1 and intermediate 2 u the dropdown menu.

ne mechanism proceeds through a first cationic intermediate, intermediate 1. Nucleophilie attacR leads 1o mtelHmet egatively charged nucleophile, the attack of the nucleophile leads directly to the product. H. Br + CH,OH Br Intermediate 1 Intermediate 2 (product) na similar fashion, draw intermediate 1 and intermediate 2 (final product) for the following reaction. OCH3 Cl2 MEOH ČI racemic mixture • Pay attention to the reactants, they may differ from the examples. In some reactions, one part of the molecule acts as the nucleophile. • You do not have to consider stereochemistry. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate intermediate 1 and intermediate 2 u the dropdown menu.

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter13: Substitution

Section: Chapter Questions

Problem 18E

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