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12. When 3,3-dimethyl-1-butene reacts with HCI, the carbocation intermediate that is formed undergoes a 1,2-methyl shift to form a more stable carbocation. Because this rearrangement takes place, the major product of the reaction is- A) 2-chloro-2,3-dimethylbutane C) 1-chloro-2,3-dimethylbutane E) 2-chloro-2-methylpentane B) 3-chloro-2,2-dimethylbutane D) 4-chloro-2,2-dimethylbutane

12. When 3,3-dimethyl-1-butene reacts with HCI, the carbocation intermediate that is formed undergoes a 1,2-methyl shift to form a more stable carbocation. Because this rearrangement takes place, the major product of the reaction is- A) 2-chloro-2,3-dimethylbutane C) 1-chloro-2,3-dimethylbutane E) 2-chloro-2-methylpentane B) 3-chloro-2,2-dimethylbutane D) 4-chloro-2,2-dimethylbutane

Curren'S Math For Meds: Dosages & Sol
Curren'S Math For Meds: Dosages & Sol
11th Edition
ISBN:9781305143531
Author:CURREN
Publisher:CURREN
Chapter6: Oral Medication Labels And Dosage Calculation
Section: Chapter Questions
Problem 9.4P
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12. When 3,3-dimethyl-1-butene reacts with HCI, the carbocation intermediate that is formed undergoes a 1,2-methyl shift to form a more stable carbocation. Because this rearrangement takes place, the major product of the reaction is- A) 2-chloro-2,3-dimethylbutane C) 1-chloro-2,3-dimethylbutane E) 2-chloro-2-methylpentane B) 3-chloro-2,2-dimethylbutane D) 4-chloro-2,2-dimethylbutane
Transcribed Image Text:12. When 3,3-dimethyl-1-butene reacts with HCI, the carbocation intermediate that is formed undergoes a 1,2-methyl shift to form a more stable carbocation. Because this rearrangement takes place, the major product of the reaction is- A) 2-chloro-2,3-dimethylbutane C) 1-chloro-2,3-dimethylbutane E) 2-chloro-2-methylpentane B) 3-chloro-2,2-dimethylbutane D) 4-chloro-2,2-dimethylbutane
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