The reaction of HBr with 1-butene produces only one product, 2- bromobutane. Why does this product form instead of 1-bromobutane? Select one: O A. Br bonds to the C-2 alkene carbon in the first step, forming the more stable carbon anion with (-) charge on C-1, followed by - bonding of H+* electrophile to (-) charged C-1. OB. There is less steric hindrance if Br" binds to C-2 and H+ bonds to C-1. O C. H bonds to the C-1 alkene carbon in the first step, forming the more stable carbocation, with (+) charge on C-2, followed by bonding of Br nucleophile to positively charged C-2. O D. H and Br know what the "EL-NM" rule is and dutifully comply with it.

The reaction of HBr with 1-butene produces only one product, 2- bromobutane. Why does this product form instead of 1-bromobutane? Select one: O A. Br bonds to the C-2 alkene carbon in the first step, forming the more stable carbon anion with (-) charge on C-1, followed by - bonding of H+* electrophile to (-) charged C-1. OB. There is less steric hindrance if Br" binds to C-2 and H+ bonds to C-1. O C. H bonds to the C-1 alkene carbon in the first step, forming the more stable carbocation, with (+) charge on C-2, followed by bonding of Br nucleophile to positively charged C-2. O D. H and Br know what the "EL-NM" rule is and dutifully comply with it.

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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