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Choose the correct statement(s) regarding Aryl and vinyl halides participation in SN2 reactions. Backside approach would be through the plane of the benzene ring. the nucleophile approaches the vinylic halides at the opposite side of the C-X carbon, in the plane of the alkene which causes Van der Waals repulsions. the nucleophile approaches the vinylic halides at the same side of the C-X carbon, in the plane of the alkene which reduces Van der Waals repulsions. □ If a vinylic halide undergos an SN2 reaction, it must form a vinylic cation. During an SN2 reaction, the carbon undergoing substitution rehybridizes to an sp3 hybrid in the transition state

Choose the correct statement(s) regarding Aryl and vinyl halides participation in SN2 reactions. Backside approach would be through the plane of the benzene ring. the nucleophile approaches the vinylic halides at the opposite side of the C-X carbon, in the plane of the alkene which causes Van der Waals repulsions. the nucleophile approaches the vinylic halides at the same side of the C-X carbon, in the plane of the alkene which reduces Van der Waals repulsions. □ If a vinylic halide undergos an SN2 reaction, it must form a vinylic cation. During an SN2 reaction, the carbon undergoing substitution rehybridizes to an sp3 hybrid in the transition state

Chemistry
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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Choose the correct statement(s) regarding Aryl and vinyl halides participation in SN2 reactions. Backside approach would be through the plane of the benzene ring. the nucleophile approaches the vinylic halides at the opposite side of the C-X carbon, in the plane of the alkene which causes Van der Waals repulsions. the nucleophile approaches the vinylic halides at the same side of the C-X carbon, in the plane of the alkene which reduces Van der Waals repulsions. □ If a vinylic halide undergos an SN2 reaction, it must form a vinylic cation. During an SN2 reaction, the carbon undergoing substitution rehybridizes to an sp3 hybrid in the transition state
Transcribed Image Text:Choose the correct statement(s) regarding Aryl and vinyl halides participation in SN2 reactions. Backside approach would be through the plane of the benzene ring. the nucleophile approaches the vinylic halides at the opposite side of the C-X carbon, in the plane of the alkene which causes Van der Waals repulsions. the nucleophile approaches the vinylic halides at the same side of the C-X carbon, in the plane of the alkene which reduces Van der Waals repulsions. □ If a vinylic halide undergos an SN2 reaction, it must form a vinylic cation. During an SN2 reaction, the carbon undergoing substitution rehybridizes to an sp3 hybrid in the transition state
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