The product below can be prepared from cyclohexanone through the following reaction sequence? A) [1] (CH3CH2)2NH, mild acid; [2] CH3CH2CH2Br, (3] HCI, H20 B) [1] CH3CH2NH2, mild acid; [2] CH3CH2CH2Br; [3] HCI, H20 9 [1] CH3OH, H+; [2] CH3CH2CH2MgBr: [3] HCI, H20 D) [1] nBuLi: (2] CH3CH2CH2Br: (3] ETNH2, mild acid E) [1] nBuli: (2] CH3CH2CH2Br; (3] Et2NH, mild acid

The product below can be prepared from cyclohexanone through the following reaction sequence? A) [1] (CH3CH2)2NH, mild acid; [2] CH3CH2CH2Br, (3] HCI, H20 B) [1] CH3CH2NH2, mild acid; [2] CH3CH2CH2Br; [3] HCI, H20 9 [1] CH3OH, H+; [2] CH3CH2CH2MgBr: [3] HCI, H20 D) [1] nBuLi: (2] CH3CH2CH2Br: (3] ETNH2, mild acid E) [1] nBuli: (2] CH3CH2CH2Br; (3] Et2NH, mild acid

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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