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.
Chapter11: Reactions Of Alkyl Halides: Nucleophilic Substitutions And Eliminations
Section11.SE: Something Extra
Problem 43AP
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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.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fb4cce8ba-46f5-4c3e-b7af-c3a8b7e8ef77%2F936799be-3751-43a1-b02a-8c336f8551a4%2Fhu8392s_processed.jpeg&w=3840&q=75)
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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