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.
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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Concept explainers
Organomagnesium compounds
The interaction of alkyl halide with Mg metal in a suitable ether solvent is the common method for the synthesis of the Grignard reagent.
Hydrolysis Grignard Reactions and Reduction
Organomagnesium halides are Grignard reagents. Francois Auguste Victor Grignard, a French chemist who received the Nobel Prize in Chemistry in 1912, created these highly useful reagents.
Question
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
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