The target compound that you should synthesize is 1-chloro-2-butene. This is an electrophilic alkene addition reaction. Examine the product to determine the location of the new functionality. Keep in mind the intermediate and the selectivity of the incoming nucleophile. A key here is the relative stabilities of the two potential products. The alkene is the electron-rich partner and an electrophilic reagent is needed. List the starting materials, solvent, reagent, and products formed:
a. How long did it take to finish the reaction?
b. What are the TLC values (R) for
1. Starting Materials
2. Products
Write a mechanism for this reaction.
Answers: 2
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The target compound that you should synthesize is 1-chloro-2-butene. This is an electrophilic alkene...
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