OBra) Heptanamide1) (Me),CuLib) MeHC-CHCOMC2) H;O- OH (aq)c) 2 AcetaldehydeBenzened) ValeramideSOCI.Heatc) 2-Octanone(Ph)sP-CH2

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Answered: - OBr a) Heptanamide 1) (Me)»CuLi b)…

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- OBr a) Heptanamide 1) (Me)»CuLi b) MeHC-CHCOMC 2) H;0 -OH (aq) c) 2 Acetaldehyde Benzene d) Valeramide SOCI2 Heat

Introduction to General, Organic and Biochemistry

11th Edition

ISBN:9781285869759

Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar Torres

Publisher:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar Torres

Chapter31: Immunochemistry

Section: Chapter Questions

Problem 31.75P

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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

OBr
a) Heptanamide
1) (Me),CuLi
b) MeHC-CHCOMC
2) H;O
- OH (aq)
c) 2 Acetaldehyde
Benzene
d) Valeramide
SOCI.
Heat
c) 2-Octanone
(Ph)sP-CH2

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