Chapter 9: Q. 9-9-8 P-b (page 272)
Using any alkyne needed, how would you prepare the following alkenes?
(b) cis-3-Heptene
Chapter 9: Q. 9-9-8 P-b (page 272)
Using any alkyne needed, how would you prepare the following alkenes?
(b) cis-3-Heptene
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Get started for freeWhich of the following bases could be used to deprotonate 1-butyne?
(a)
Occasionally, a chemist might need to invert the stereochemistry of an alkene—that is, to convert a cis alkene to a trans alkene, or vice versa. There is no one-step method for doing an alkene inversion, but the transformation can be carried out by combining several reactions in the proper sequence. How would you carry out the following reactions?
(a)
(b)
1-Octen-3-ol, a potent mosquito attractant commonly used in mosquito traps, can be prepared in two steps from hexanal, . The first step is an acetylide-addition reaction like that described in Problem 9-50. What is the structure of the product from the first step, and how can it be converted into 1-octen-3-ol?
Draw structures corresponding to the following names:
(a)3,3-Dimethyl-4-octyne
(b)3-Ethyl-5-methyl-1,6,8-decatriyne
(c)2,2,5,5-Tetramethyl-3-hexyne
(d)3,4-Dimethylcyclodecyne
(e)3,5-Heptadien-1-yne
(f)3-Chloro-4,4-dimethyl-1-nonen-6-yne
(g)3-sec-Butyl-1-heptyne
(h)5-tert-Butyl-2-methyl-3-octyne
Arrange the carbocations below in order of increasing stability.
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