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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 SOC 2 and pyridine with an alcohol proceeds via an SN2 mechanism OH OH OH HOlle e. Goal: determine the stereoselectivity or stereospecificity of alkene dihydroxylation using OsO4 in water ん

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 SOC 2 and pyridine with an alcohol proceeds via an SN2 mechanism OH OH OH HOlle e. Goal: determine the stereoselectivity or stereospecificity of alkene dihydroxylation using OsO4 in water ん

Organic Chemistry: A Guided Inquiry
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 SOC 2 and pyridine with an alcohol proceeds via an SN2 mechanism OH OH OH HOlle e. Goal: determine the stereoselectivity or stereospecificity of alkene dihydroxylation using OsO4 in water ん
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 SOC 2 and pyridine with an alcohol proceeds via an SN2 mechanism OH OH OH HOlle e. Goal: determine the stereoselectivity or stereospecificity of alkene dihydroxylation using OsO4 in water ん
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