1. Provide the structures for all possible products (more than two, less than five) of radical allylic bromination of the compound below. Be sure to analyze all resonance structures to be complete. Me Me NBS hv

1. Provide the structures for all possible products (more than two, less than five) of radical allylic bromination of the compound below. Be sure to analyze all resonance structures to be complete. Me Me NBS hv

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter8: Addition Via Carbocation

Section: Chapter Questions

Problem 9E

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Concept explainers

Reactions of Ethers

Ethers (R-O-R’) are compounds formed by replacing hydrogen atoms of an alcohol (R-OH compound) or a phenol (C6H5OH) by an aryl/ acyl group (functional group after removing single hydrogen from an aromatic ring). In this section, reaction, preparation and behavior of ethers are discussed in the context of organic chemistry.

Epoxides

Epoxides are a special class of cyclic ethers which are an important functional group in organic chemistry and generate reactive centers due to their unusual high reactivity. Due to their high reactivity, epoxides are considered to be toxic and mutagenic.

Williamson Ether Synthesis

An organic reaction in which an organohalide and a deprotonated alcohol forms ether is known as Williamson ether synthesis. Alexander Williamson developed the Williamson ether synthesis in 1850. The formation of ether in this synthesis is an SN2 reaction.

Question

1. Provide the structures for all possible products (more than two, less than five) of radical
allylic bromination of the compound below. Be sure to analyze all resonance structures to be
complete.
Me.
Me
NBS
hv

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