4. In each case below, circle the starting material that would best serve the experimental design goal. Assume each option is a single stereoisomer, where applicable. 5 points a. Goal: determine whether or not acid-catalyzed hydration of alkenes is regioselective b. Goal: determine whether or not epoxide formation from halohydrins is stereospecific C. Goal: determine whether acid-catalyzed dehydration of alcohols proceeds via an E1 or E2 mechanism. OH OH OH OH d. Goal: determine whether or not the reaction of SOCI₂ and pyridine with an alcohol proceeds via an SN2 mechanism OH e. OH OH HOlle Goal: determine the stereoselectivity or stereospecificity of alkene dihydroxylation using OsO4 in water
4. In each case below, circle the starting material that would best serve the experimental design goal. Assume each option is a single stereoisomer, where applicable. 5 points a. Goal: determine whether or not acid-catalyzed hydration of alkenes is regioselective b. Goal: determine whether or not epoxide formation from halohydrins is stereospecific C. Goal: determine whether acid-catalyzed dehydration of alcohols proceeds via an E1 or E2 mechanism. OH OH OH OH d. Goal: determine whether or not the reaction of SOCI₂ and pyridine with an alcohol proceeds via an SN2 mechanism OH e. OH OH HOlle Goal: determine the stereoselectivity or stereospecificity of alkene dihydroxylation using OsO4 in water
Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter13: Substitution
Section: Chapter Questions
Problem 4E
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![4. In each case below, circle the starting material that would best serve the experimental design
goal. Assume each option is a single stereoisomer, where applicable. 5 points
a. Goal: determine whether or not acid-catalyzed hydration of alkenes is regioselective
b. Goal: determine whether or not epoxide formation from halohydrins is stereospecific
C. Goal: determine whether acid-catalyzed dehydration of alcohols proceeds via an E1 or
E2 mechanism.
OH
OH
OH
OH
d. Goal: determine whether or not the reaction of SOCI₂ and pyridine with an alcohol
proceeds via an SN2 mechanism
OH
e.
OH
OH
HOlle
Goal: determine the stereoselectivity or stereospecificity of alkene dihydroxylation using
OsO4 in water](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F55bef063-ab80-471e-b8ef-db672c4a154c%2F44b39ca3-0e31-4aa6-a724-d2f818c3a773%2Fakpa2go_processed.png&w=3840&q=75)
Transcribed Image Text:4. In each case below, circle the starting material that would best serve the experimental design
goal. Assume each option is a single stereoisomer, where applicable. 5 points
a. Goal: determine whether or not acid-catalyzed hydration of alkenes is regioselective
b. Goal: determine whether or not epoxide formation from halohydrins is stereospecific
C. Goal: determine whether acid-catalyzed dehydration of alcohols proceeds via an E1 or
E2 mechanism.
OH
OH
OH
OH
d. Goal: determine whether or not the reaction of SOCI₂ and pyridine with an alcohol
proceeds via an SN2 mechanism
OH
e.
OH
OH
HOlle
Goal: determine the stereoselectivity or stereospecificity of alkene dihydroxylation using
OsO4 in water
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