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

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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