Chapter 7: Q35P (page 314)
Draw the mechanism for the following reaction
Addition of Br2 to the triple bond in the presence of H2O forms an enol that immediately tautomerizes to a ketone.
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Why does cis-2-butene have a higher boiling point than trans-2-butene?
How could the following compounds be synthesized from acetylene?
What ketones would be formed from the acid-catalyzed addition of water to 3-heptyne?
Describe the alkyne you would start with and the reagents you would use if you wanted to Synthesize
a. Pentane. b. Cis-2-butene. c. trans-2-pentene. d. 1-hexene.
What is the major product of each of the following reactions?
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