B. Consider the free-radical monobromination reaction of (S)-2-bromobutane. The reaction produces five monobromination products whose structures are shown below. CH3 CH,Br CH3 CH3 Br2 ► H UV Br Br H- Br Br H- Br CH,CH3 CH2CH2Br II CH2CH3 CH2CH3 (S)-2-bromobutane CH3 CH3 H- Br H- Br H- Br Br H. CH3 ČH3 V IV 1. Which of the following products are optically active (OA)? Which are optically inactive (OI)? A: 2. The products are separated from each other using fractional distillation (separation based on difference in boiling points). How many fractions should be obtained assuming that all compounds with distinct boiling points are completely separated from each other?
B. Consider the free-radical monobromination reaction of (S)-2-bromobutane. The reaction produces five monobromination products whose structures are shown below. CH3 CH,Br CH3 CH3 Br2 ► H UV Br Br H- Br Br H- Br CH,CH3 CH2CH2Br II CH2CH3 CH2CH3 (S)-2-bromobutane CH3 CH3 H- Br H- Br H- Br Br H. CH3 ČH3 V IV 1. Which of the following products are optically active (OA)? Which are optically inactive (OI)? A: 2. The products are separated from each other using fractional distillation (separation based on difference in boiling points). How many fractions should be obtained assuming that all compounds with distinct boiling points are completely separated from each other?
Chemistry
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ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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Chapter1: Chemical Foundations
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Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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III. B 1-2
![B. Consider the free-radical monobromination reaction of (S)-2-bromobutane. The reaction produces
five monobromination products whose structures are shown below.
CH3
CH,Br
CH3
CH3
Br2
H-
Br
Br
Br
-Br
Br
UV
CH2CH2Br
II
CH,CH3
CH2CH3
CH2CH3
(S)-2-bromobutane
CH3
CH3
Br
H-
Br
H Br
Br H
CH3
CH3
V
IV
1. Which of the following products are optically active (OA)? Which are
optically inactive (OI)?
OA:
Ol:
2. The products are separated from each other using fractional distillation
(separation based on difference in boiling points). How many fractions
should be obtained assuming that all compounds with distinct boiling
points are completely separated from each other?](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fe00fd7e2-4f95-4f07-b378-3b9a77a9bd1b%2Fb21f41e4-2fb3-4099-a1e0-7a97f5e46af6%2Fdadpl4_processed.jpeg&w=3840&q=75)
Transcribed Image Text:B. Consider the free-radical monobromination reaction of (S)-2-bromobutane. The reaction produces
five monobromination products whose structures are shown below.
CH3
CH,Br
CH3
CH3
Br2
H-
Br
Br
Br
-Br
Br
UV
CH2CH2Br
II
CH,CH3
CH2CH3
CH2CH3
(S)-2-bromobutane
CH3
CH3
Br
H-
Br
H Br
Br H
CH3
CH3
V
IV
1. Which of the following products are optically active (OA)? Which are
optically inactive (OI)?
OA:
Ol:
2. The products are separated from each other using fractional distillation
(separation based on difference in boiling points). How many fractions
should be obtained assuming that all compounds with distinct boiling
points are completely separated from each other?
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