ORGANIC CHEMISTRY (LOOSELEAF)-PACKAGE
ORGANIC CHEMISTRY (LOOSELEAF)-PACKAGE
10th Edition
ISBN: 9781260008562
Author: Carey
Publisher: MCG
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Chapter 23, Problem 17P
Interpretation Introduction

Interpretation: The reasonable structure of the compound that results by the reaction of phenol with 1,2-epoxypropane in aqueous sodium hydroxide at 15οC is to be drawn.

Concept introduction:

Phenols contain hydroxyl (OH) functional group attached to an aromatic ring.

Phenol is acidic in nature and in the presence of a strong base such as sodium hydroxide, the formation of phenoxide ion occurs after the abstraction of proton by hydroxide ion. The phenoxide ion acts as a nucleophile.

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NAME: 1. Draw the major product of the following E2 reaction. Make sure you pay attention to REGIOCHEMISTRY and STEREOCHEMISTRY. To get credit for this question, you must EXPLAIN how you got your answer using STRUCTURES and WORDS. Br NaOCH3 acetone F2 reaction To get credit for this
3. Reactions! Fill in the information missing below. Make sure to pay attention to REGIOCHEMISTRY and STEREOCHEMISTRY. Br2 CH3OH + 4. Mechanism! Show the complete arrow pushing mechanism, including all steps and intermediates for the following reactions. To get credit for this, you MUST show how ALL bonds are broken and formed, using arrows to show the movement of electrons. H3O+ HO
Please provide a synthesis for the Ester using proponoic acid, thank you!
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