wwwww 1. With regards to regioselectivity in the addition reactions of alkenes, what is Markovnikov's rule? (1 point) when un symmetrical alkenes combine hydrohalic acids, the halogen adds to the carbon with the least amount of hydrogen atoms 2. In the bromination reaction of E-stilbene, why is Markovnikov's rule irrelevant? (1 point) Alkenes react with diatomic halogens to form electrophilic addition products. 3. In the bromination reaction of E-stilbene, why don't carbocation rearrangements occur? (1 point) Reaction is through a halonium ion instead of a carbocation. 4. In the bromination reaction of E-stilbene, why does anti addition take place instead of syn addition? (2 points) 5. Draw the complete curved-arrow mechanism for the bromination of trans-stilbene. Do not copy and paste from someone else's work, must be original. (3 points)
wwwww 1. With regards to regioselectivity in the addition reactions of alkenes, what is Markovnikov's rule? (1 point) when un symmetrical alkenes combine hydrohalic acids, the halogen adds to the carbon with the least amount of hydrogen atoms 2. In the bromination reaction of E-stilbene, why is Markovnikov's rule irrelevant? (1 point) Alkenes react with diatomic halogens to form electrophilic addition products. 3. In the bromination reaction of E-stilbene, why don't carbocation rearrangements occur? (1 point) Reaction is through a halonium ion instead of a carbocation. 4. In the bromination reaction of E-stilbene, why does anti addition take place instead of syn addition? (2 points) 5. Draw the complete curved-arrow mechanism for the bromination of trans-stilbene. Do not copy and paste from someone else's work, must be original. (3 points)
Organic Chemistry
8th Edition
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Chapter21: Benzene And The Concept Of Aromaticity
Section: Chapter Questions
Problem 21.44P
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