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Show how you would synthesize octanal from each compound. You may use any necessary reagents. (a) octan-1-ol (b) non- 1 -ene (c) oct-1-yne (d) 1 -bromoheptane (e) 1 -bromohexane (f) octanoic acid (g) ethyl octanoate | Numerade
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Oct 28, 2020
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SOLVED: Outline the steps in the E1 reaction of (CH3)3CCl in ethanolwith a low NaOEt concentration. a. What other products will beformed? b. Compare the rates of formation of the two products.
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