(b)(c)A-2.Give the structure of the reactant, reagent, or product omitted from each of the followingreactions.(a)(b)(c)(d)(e)(f)(g)(h)A-3.Which one of the following two reactions is effective in the synthesis of 4-methyl-2-hexyne?Why is the other not effective?1.2.A-4.Outline a series of steps, using any necessary organic and inorganic reagents, for the prepa-ration of:(a)1-Butyne from ethyl bromide as the source of all carbon atoms(b)3-Hexyne from 1-butyne(c)3-Hexyne from 1-butene(d)A-5.Treatment of propyne in successive steps with sodium amide, 1-bromobutane, and sodium inliquid ammonia yields as the fnal product ______.A-6.Give the structures of compounds A through D in the following series of equations.
This is the end of the preview. Sign up
access the rest of the document.
This note was uploaded on 09/26/2011 for the course CHM 2210 taught by Professor Reynolds during the Fall '01 term at University of Florida.