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.

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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1
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