Select from the Table provided the reagent you would use to carry out each of the transformations below. Reagents Availableа. КОНe. Hg(OAc)2, H2O; then NaBH4i. O3; then Zn, H30*b. KMNO4, H3O*f. OsO4; then NaHSO3j. H2SO4С. На, Pdg. ВН3; then Hz02, "ОНk. Cl2d. CH212, Zn(Cu)h. СHCIl3, КОНI. CIco,H , then H30*CH3CH3?FHO-OH?CHCH3-CHCH3

For the transformation following reagents were used-

Answered: Select from the Table provided the…

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Chemistry

Select from the Table provided the reagent you would use to carry out each of the transformations below

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter14: Conjugated Compounds And Ultraviolet Spectroscopy

Section14.SE: Something Extra

Problem 66AP

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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

Select from the Table provided the reagent you would use to carry out each of the transformations below.

Reagents Available
а. КОН
e. Hg(OAc)2, H2O; then NaBH4
i. O3; then Zn, H30*
b. KMNO4, H3O*
f. OsO4; then NaHSO3
j. H2SO4
С. На, Pd
g. ВН3; then Hz02, "ОН
k. Cl2
d. CH212, Zn(Cu)
h. СHCIl3, КОН
I. CI
co,H , then H30*
CH3
CH3
?
FHO-
OH
?
CHCH3
-CHCH3

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