Chemistry
Chemistry
10th Edition
ISBN: 9781305957404
Author: Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher: Cengage Learning
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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)
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Transcribed Image Text: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)
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