B. Describe the stereochemistry (with structures) of the addition of Br₂ and H₂O to cyclohexene. C. Arrange the following ions by increasing basicity, where 1 is the most basic and 5 is the least. HCEC O CH3CH3NH2 CH₂CH₂0 CH3CH2 H₂C=CH

B. Describe the stereochemistry (with structures) of the addition of Br₂ and H₂O to cyclohexene. C. Arrange the following ions by increasing basicity, where 1 is the most basic and 5 is the least. HCEC O CH3CH3NH2 CH₂CH₂0 CH3CH2 H₂C=CH

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter5: Stereochemistry At Tetrahedral Centers

Section5.SE: Something Extra

Problem 70AP

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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

B. Describe the stereochemistry (with structures) of the addition of Br2 and H₂O to cyclohexene.
C. Arrange the following ions by increasing basicity, where 1 is the most basic and 5 is the least.
HCEC
CH3CH3NH2
CH3CH₂O
CH3CH₂
H₂C=CH

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