QUESTION 20 Which observation is NOT consistent with an SN1 mechanism for the conversion alkyl halide? OA Reaction of 2-methylcyclohexanol with H-Br gives 1-bromo-1-methylcyclohexane as the major product. an alcohol into an O B. Methylcyclohexanol is more reactive than 2-methylcyclohexanol towards H-CI. OC Doubling the concentration of chloride ion will double the rate of formation of 2-chloro- 2-methylhexane from 2-methylhexan-2-ol. OD Reaction of R-3-methyl-heptan-3-ol with HI provides a racemic mixture of 3R and 3S 3-iodo- 3-methylheptane.

QUESTION 20 Which observation is NOT consistent with an SN1 mechanism for the conversion alkyl halide? OA Reaction of 2-methylcyclohexanol with H-Br gives 1-bromo-1-methylcyclohexane as the major product. an alcohol into an O B. Methylcyclohexanol is more reactive than 2-methylcyclohexanol towards H-CI. OC Doubling the concentration of chloride ion will double the rate of formation of 2-chloro- 2-methylhexane from 2-methylhexan-2-ol. OD Reaction of R-3-methyl-heptan-3-ol with HI provides a racemic mixture of 3R and 3S 3-iodo- 3-methylheptane.

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter16: Chemistry Of Benzene: Electrophilic Aromatic Substitution

Section16.SE: Something Extra

Problem 30MP: The carbocation electrophile in a Friede1-Crafts reaction can be generated by an alternate means...

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