(R)-2-iodo-3-methylbutane is treated with sodium bromide in acetone. Select all products that are formed. 2-methylbutan-1-ol 2-methylbutan-2-ol 3-methylbut-1-ene (R)-3-methyl-2-butanol 2-methylbut-2-ene O (S)-2-bromo-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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(R)-2-iodo-3-methylbutane is treated with sodium bromide in acetone. Select all products that are formed.
2-methylbutan-1-ol
2-methylbutan-2-ol
3-methylbut-1-ene
(R)-3-methyl-2-butanol
2-methylbut-2-ene
O (S)-2-bromo-3-methylbutane
Transcribed Image Text:(R)-2-iodo-3-methylbutane is treated with sodium bromide in acetone. Select all products that are formed. 2-methylbutan-1-ol 2-methylbutan-2-ol 3-methylbut-1-ene (R)-3-methyl-2-butanol 2-methylbut-2-ene O (S)-2-bromo-3-methylbutane
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