Part A Why is the E1 not a likely mechanism when 1-chloropentane is heated in ethanol? The substrate is too hindered. Ethanol is a poor base to use in E1 reactions. The C-H and C-Cl bonds which need to break cannot achieve an anti-periplanar orientation. Primary halides cannot undergo E1 reactions. E1 reactions cannot proceed in polar protic solvents. Submit Request Answer

Part A Why is the E1 not a likely mechanism when 1-chloropentane is heated in ethanol? The substrate is too hindered. Ethanol is a poor base to use in E1 reactions. The C-H and C-Cl bonds which need to break cannot achieve an anti-periplanar orientation. Primary halides cannot undergo E1 reactions. E1 reactions cannot proceed in polar protic solvents. Submit Request Answer

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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