Consider the following mechanism of reaction:CH3CH,CH3CH;C CH, + H-CICH;CCH, + C: → CH;CCH,tert-butyl cationCItert-butyl chlorideIn this reaction:The alkene and the carbocation intermediate are both nucleophilicHCl and CI" are both nucleophilicThe alkene and HCI are both electrophilicThe carbocation and CI" are both electrophilicThe alkene and CI" are both nucleophilicAMeving to another question will save this response

The nucleophile is the nucleus loving. This means they have enough electron to donate.

Consider the following mechanism of reaction: CH CH CH;C-CH, + H-CI CH;CCH; + CI: → CH;CCH, tert-butyl cation CI tert-butyl chloride In this reaction: The alkene and the carbocation intermediate are both nucleophilic O HCI and cr are both nucleophilic The alkene and HCI are both electrophilic The carbocation and CI are both electrophilic The alkene and CI" are both nucleophilic

Consider the following mechanism of reaction: CH CH CH;C-CH, + H-CI CH;CCH; + CI: → CH;CCH, tert-butyl cation CI tert-butyl chloride In this reaction: The alkene and the carbocation intermediate are both nucleophilic O HCI and cr are both nucleophilic The alkene and HCI are both electrophilic The carbocation and CI are both electrophilic The alkene and CI" are both nucleophilic

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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