Pls solve D,E,F and G parts Suggest readily available starting materials and reaction conditions suitable forobtaining each of the following compounds by a procedure involving alkylation ofnucleophilic carbon.(a) PHCH2CH2CHPH(b) (CH3)½C=CHCH2CH2CCH2CO;CH3ČN(c)(d) CH2=CHCH=CHCH2CH2CO,HCH3CH2CO2HCH3CH3COCH;CH2CH2(f)(e) 2,3-diphenylpropanoic acid(g)CH3OʻCH3CH2 CH2CH=CH2

Answered: Image /qna-images/answer/905b67ff-bce5-4545-a5ff-6860f0a7383e.jpg

Answered: (с) (d) CH2=CHCH=CHCH;CH;CO2H CH3…

(с) (d) CH2=CHCH=CHCH;CH;CO2H CH3 CH2CO2H CH3 CH;CO I (f) CH;CCH;CH2* (e) 2,3-diphenylpropanoic acid (g) CH3O´ CH3CH2 CH2CH=CH2

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter22: Carbonyl Alpha-substitution Reactions

Section22.SE: Something Extra

Problem 26MP: Nonconjugated , -unsaturated ketones, such as 3-cyclohexenone, are in an acid-catalyzed equilibrium...

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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

Pls solve

D,E,F and G parts

Suggest readily available starting materials and reaction conditions suitable for
obtaining each of the following compounds by a procedure involving alkylation of
nucleophilic carbon.
(a) PHCH2CH2CHPH
(b) (CH3)½C=CHCH2CH2CCH2CO;CH3
ČN
(c)
(d) CH2=CHCH=CHCH2CH2CO,H
CH3
CH2CO2H
CH3
CH3CO
CH;CH2CH2
(f)
(e) 2,3-diphenylpropanoic acid
(g)
CH3Oʻ
CH3CH2 CH2CH=CH2

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