The reaction below precedes via an E2 elimination versus an SN2 reaction. Circle all of the answers that correctly support this reaction outcome. NaOCH3 + Naci CH;OH The nucleophilicity of the methoxide anion (CH3O) is reduced in protic solvent The primary alkyl halide provides too much sterics for an effective SN2 reaction to occur Sodium methoxide (NaOCH3) is a strong enough base to deprotonate the alkyl chloride Stable primary carbocations can form beta-hydrogens on the carbon adjacent to the chloro group are available for deprotonation O O 0 00
The reaction below precedes via an E2 elimination versus an SN2 reaction. Circle all of the answers that correctly support this reaction outcome. NaOCH3 + Naci CH;OH The nucleophilicity of the methoxide anion (CH3O) is reduced in protic solvent The primary alkyl halide provides too much sterics for an effective SN2 reaction to occur Sodium methoxide (NaOCH3) is a strong enough base to deprotonate the alkyl chloride Stable primary carbocations can form beta-hydrogens on the carbon adjacent to the chloro group are available for deprotonation O O 0 00
Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter9: Addition Via Cyclic Intermediate
Section: Chapter Questions
Problem 3CTQ
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