36. The ring-opening of cyclic ethers happens through cleavage by suitable nucleophiles. Which among the structures below will be the most susceptible to ring- opening? A. B. C. D.

Organic Chemistry
8th Edition
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Chapter11: Ethers, Epoxides, And Sulfides
Section11.4: Preparation Of Ethers
Problem 11.3P: Show how you might use the Williamson ether synthesis to prepare each ether. (a) (b)
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Aldehydes undergo nucleophilic addition reactions with potent nucleophiles such as water, alcohol and amino compounds. Which of the following nucleophiles will exhibit the greatest ability to attack the electrophilic carbon in the carbonyl group of ethanal?
Group of answer choices
cyclohexyl alcohol
para-chlorophenol
isoamyl alcohol
ortho-aminophenol
 
An aromatic ring should satisfy Huckel’s rule, wherein the number of electrons participating in the cyclic conjugation should be equal to 4n + 2. Which of the following cyclic structures does NOT obey Huckel’s rule?
Group of answer choices
Cyclobutadienyl dianion
Tetrahydrofuran ring
Cyclopropene structure
Pyrimidine ring structure
36. The ring-opening of cyclic ethers happens through cleavage by suitable
nucleophiles. Which among the structures below will be the most susceptible to ring-
opening?
A.
B.
C.
D.
Transcribed Image Text:36. The ring-opening of cyclic ethers happens through cleavage by suitable nucleophiles. Which among the structures below will be the most susceptible to ring- opening? A. B. C. D.
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