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.
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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![QUESTION 20
Which observation is NOT consistent with an SN1 mechanism for the conversion of an alcohol into an
alkyl halide?
O A. Reaction of 2-methylcyclohexanol with H-Br gives 1-bromo-1-methylcyclohexane as the major
product.
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.
O D. Reaction of R-3-methyl-heptan-3-ol with HI provides a racemic mixture of 3R and 3S 3-iodo-
3-methylheptane.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F7ab4781e-24b4-492f-8d61-3c52a5ea0f2b%2F68bfb105-2f91-4f7e-bd91-e5a6b66e3cb8%2F96ovrud_processed.jpeg&w=3840&q=75)
Transcribed Image Text:QUESTION 20
Which observation is NOT consistent with an SN1 mechanism for the conversion of an alcohol into an
alkyl halide?
O A. Reaction of 2-methylcyclohexanol with H-Br gives 1-bromo-1-methylcyclohexane as the major
product.
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.
O D. Reaction of R-3-methyl-heptan-3-ol with HI provides a racemic mixture of 3R and 3S 3-iodo-
3-methylheptane.
![QUESTION 21
Which of the following species will have a formal positive charge on the carbon atom?
O A CH3 with an empty p orbital.
O B.
CH2 with an empty p orbital and a filled sp2 orbital.
OC CH3 with a half filled p orbital.
OD.
CH3 with a filled sp3 orbital.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F7ab4781e-24b4-492f-8d61-3c52a5ea0f2b%2F68bfb105-2f91-4f7e-bd91-e5a6b66e3cb8%2Fy3wue35_processed.jpeg&w=3840&q=75)
Transcribed Image Text:QUESTION 21
Which of the following species will have a formal positive charge on the carbon atom?
O A CH3 with an empty p orbital.
O B.
CH2 with an empty p orbital and a filled sp2 orbital.
OC CH3 with a half filled p orbital.
OD.
CH3 with a filled sp3 orbital.
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