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Which observation is NOT consistent with an SN1 mechanism for the conversion of an alcohol Into an alkyl hallde? OA Doubling the concentration of lodide lon wiIl double the rate of formation of 2-lodo-2- methylhexane from 2-methylhexan-2-ol. OR Methylcyclohexanol is more reactive than 2-methylcyclohexanol towards H-I. OCReaction of R-3-methyl-heptan-3-ol with HCI provides a racemic mixture of 3R and 35 3-chloro-3- methylheptane. ODReaction of 2-methylcyclohexanol with H-Br gives 1-bromo-1-methylcyclohexane as the major product.

Which observation is NOT consistent with an SN1 mechanism for the conversion of an alcohol Into an alkyl hallde? OA Doubling the concentration of lodide lon wiIl double the rate of formation of 2-lodo-2- methylhexane from 2-methylhexan-2-ol. OR Methylcyclohexanol is more reactive than 2-methylcyclohexanol towards H-I. OCReaction of R-3-methyl-heptan-3-ol with HCI provides a racemic mixture of 3R and 35 3-chloro-3- methylheptane. ODReaction of 2-methylcyclohexanol with H-Br gives 1-bromo-1-methylcyclohexane as the major product.

Organic Chemistry: A Guided Inquiry
Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter14: Elimination
Section: Chapter Questions
Problem 3E
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Which observation is NOT consistent with an SN1 mechanism for the conversion of an alcohol Into an alkyl hallde? OA Doubling the concentration of lodide lon wiIl double the rate of formation of 2-lodo-2- methylhexane from 2-methylhexan-2-ol. On Methylcyclohexanol is more reactive than 2-methylcyclohexanol towards H-1. OC Reaction of R-3-methyl-heptan-3-ol with HCI provides a racemic mixture of 3R and 35 3-chloro-3- methylheptane. OD Reaction of 2-methylcyclohexanol with H-Br gives 1-bromo-1-methylcyclohexane as the major product.
Transcribed Image Text:Which observation is NOT consistent with an SN1 mechanism for the conversion of an alcohol Into an alkyl hallde? OA Doubling the concentration of lodide lon wiIl double the rate of formation of 2-lodo-2- methylhexane from 2-methylhexan-2-ol. On Methylcyclohexanol is more reactive than 2-methylcyclohexanol towards H-1. OC Reaction of R-3-methyl-heptan-3-ol with HCI provides a racemic mixture of 3R and 35 3-chloro-3- methylheptane. OD Reaction of 2-methylcyclohexanol with H-Br gives 1-bromo-1-methylcyclohexane as the major product.
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