8. Which compound reacts most rapidly with cyanide ion in a polar, aprotic solvent? (A) 2-chloro-2-methylbutane (B) 2-bromo-2-methylbutane (C) 1-chloro-2-methylbutane (D) 1-chloro-3-methylbutane

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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8. Which compound reacts most rapidly with cyanide ion in
a polar, aprotic solvent?
(A) 2-chloro-2-methylbutane
(B) 2-bromo-2-methylbutane
(C) 1-chloro-2-methylbutane
(D) 1-chloro-3-methylbutane
Transcribed Image Text:8. Which compound reacts most rapidly with cyanide ion in a polar, aprotic solvent? (A) 2-chloro-2-methylbutane (B) 2-bromo-2-methylbutane (C) 1-chloro-2-methylbutane (D) 1-chloro-3-methylbutane
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