1. As we've seen, SN1/E1 reactions can be quite messy and can generate multiple products. Consider the reaction shown in order to answer questions a-c. a. Draw the carbocation intermediate that is formed during the SN1/El reaction in Box 1. Вох 1 'Br ELOH Carbocation b. Draw ALL possible elimination and substitution products that can be formed from the carbocation you drew in part a, and label the most and least stable alkene products. (Hint: There are 5 possible products.) Substitution Elimination c. Now, draw the arrow-pushing mechanism for the El reaction that forms most stable alkene product. "Br EŁOH

Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter25: Enolate & Enol Nucleophiles
Section: Chapter Questions
Problem 11CTQ
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1. As we've seen, SN1/El reactions can be quite messy and can generate multiple products.
Consider the reaction shown in order to answer questions a-c.
a. Draw the carbocation intermediate that is formed during the SN1/E1 reaction in Box 1.
Вох 1
Br
ELOH
Carbocation
b. Draw ALL possible elimination and substitution products that can be formed from the
carbocation you drew in part a, and label the most and least stable alkene products.
(Hint: There are 5 possible products.)
Elimination
Substitution
c. Now, draw the arrow-pushing mechanism for the El reaction that forms most stable
alkene product.
'Br
EŁOH
Transcribed Image Text:1. As we've seen, SN1/El reactions can be quite messy and can generate multiple products. Consider the reaction shown in order to answer questions a-c. a. Draw the carbocation intermediate that is formed during the SN1/E1 reaction in Box 1. Вох 1 Br ELOH Carbocation b. Draw ALL possible elimination and substitution products that can be formed from the carbocation you drew in part a, and label the most and least stable alkene products. (Hint: There are 5 possible products.) Elimination Substitution c. Now, draw the arrow-pushing mechanism for the El reaction that forms most stable alkene product. 'Br EŁOH
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