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Your goal is to synthesize a disubstituted alkyne in 4 steps starting with ethyne as the source of your triple bond. Steps 1 and 3 are the steps using sodium amide. Select all of the species that could be used for steps 2 and 4 to accomplish your goal in good yield. a) isopropyl iodide b) ethylmagnesium bromide c) HBr d) 1-chloro-4-methylpentane e) ethoxide ion f) methanol g) hexan-1-ol h) bromoethane i) methyl tosylate j) iodocyclohexane
Sagot :
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