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
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
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](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fe830fdc0-502e-4879-ad61-05e8994339ec%2F43f2303e-11e4-4081-8645-df71c4426f1c%2Fgngpwg_processed.jpeg&w=3840&q=75)
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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