The SN1 reaction is a two-step reaction, and the first step of this reaction is the formation of a carbocation intermediate. Draw the carbocation intermediates that form from the alkyl chlorides in tubes 8 and 15. 2. Again, use tubes 8 and 15 to answer the following question. In
The SN1 reaction is a two-step reaction, and the first step of this reaction is the formation of a carbocation intermediate. Draw the carbocation intermediates that form from the alkyl chlorides in tubes 8 and 15. 2. Again, use tubes 8 and 15 to answer the following question. In
Macroscale and Microscale Organic Experiments
7th Edition
ISBN:9781305577190
Author:Kenneth L. Williamson, Katherine M. Masters
Publisher:Kenneth L. Williamson, Katherine M. Masters
Chapter16: The Sn2 Reaction: 1-bromobutane
Section: Chapter Questions
Problem 7Q
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- The SN1 reaction is a two-step reaction, and the first step of this reaction is the formation of a carbocation intermediate. Draw the carbocation intermediates that form from the alkyl chlorides in tubes 8 and 15.
2. Again, use tubes 8 and 15 to answer the following question. In general, the more stable carbocation forms faster. Given this, which carbocation is more stable, or do they have the same stability?
![8
1-chlorobutane
1-bromobutane
1-iodobutane
11
2-chlorobutane
12
2-bromobutane
2-chloro-2-
methylpropane
(t-butyl chloride)
13
2-bromo-2-
14
methylpropane
(t-butyl bromide)
3-chloro-1-propene
(allyl chloride)
15
10](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F706fa0bc-8b2b-46b5-9a0a-aff6b909f26f%2Fcc2497a2-ec13-4ee6-a048-4327449a69ad%2Fnbg290h_processed.png&w=3840&q=75)
Transcribed Image Text:8
1-chlorobutane
1-bromobutane
1-iodobutane
11
2-chlorobutane
12
2-bromobutane
2-chloro-2-
methylpropane
(t-butyl chloride)
13
2-bromo-2-
14
methylpropane
(t-butyl bromide)
3-chloro-1-propene
(allyl chloride)
15
10
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