ORGANIC CHEMISTRY
ORGANIC CHEMISTRY
9th Edition
ISBN: 9780134645704
Author: WADE AND SIMEK
Publisher: PEARSON
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Chapter 15, Problem 15.39SP
Interpretation Introduction

To determine: The structures of an intermediate and the final product, with particular attention to their stereochemistry.

Interpretation: The structures of the intermediate and the final product, with particular attention to their stereochemistry are to be predicted.

Concept introduction: Cycloaddition reactions involve the addition of two or more unsaturated cyclic molecules. There is no need of nucleophile and an electrophile in these types of reactions.

Stereochemistry is the branch of chemistry that deals with 3D arrangement of molecules.

Decarboxylation reaction involves the release of carbon dioxide to form a product through the removal of carboxyl group. The reverse process is known as carboxylic reaction.

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2. Name the following hydrocarbons. (9 marks) a) HHHHHHHH H-C-C- H-O-S b) HCEC-CH3 H H H H H d) c) H C=C- H H H e) CH3 CH3 CH2CH=CH-CH=CHCH3 HHHH H-C-C-C-C-H H HH H f) large CH2CH3 pola H3C section lovels tower, able ocart firs g) Tower H3C-CH2 then in H3C-CH-CH-CH3 enblbano bne noitsidab Copyright © 2008. Durham Continuing Education CH3
Name the molecules & Identify any chiral center CH3CH2CH2CHCH₂CH₂CH₂CH₂ OH CH₂CHCH2CH3 Br CH3 CH3CHCH2CHCH2CH3 CH3
Curved arrows are used to illustrate the flow of electrons. Using the provided starting and product structures, draw the curved electrons-pushing arrows for the following reaction or mechanistic step(s).

Chapter 15 Solutions

ORGANIC CHEMISTRY

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