Predict the structure of the major product formed by 1,2-addition of HCl to 2,3,5-trimethyl-2,4-hexadiene

Synthesize 2-bromo-3-methylbutane from 2-methylbutane

Provide the structure of the two organic product(s) which results when 2-bromo-2-methylbutane is treated with sodium ethoxide.

Draw the structure of the starting material needed to make 2-methylhept-3-yne using sodium amide in liquid ammonia, followed by 1-bromopropane. The starting hydrocarbon must have no more than five carbons 1) NaNH2, NH3() NaBr + 2) CHзCH2CH2Br

Show how the reaction of an allylic halide with a Grignard reagent might be used to synthesize the following hydrocarbons.(a) 5-methylhex-1-ene

The academic version of the process invention program (PIP) contains several examples, as follows: HDAl-hydrodealkylation of toluene to produce benzene CYHEXl-cyclohexane production by hydrogenation of benzene STYRl-styrene production from ethylbenzene XYLl-production of m-xylene from toluene ANHYDl-reaction of acetone and acetic acid to form acetic anhydride BUTALl-alkylation reaction of butene-1 and isobutane to produce iso-octane Select the “new plant design” mode and the “look at existing flow sheet” option, and follow the synthesis steps for one of these processes. ‘Obtain the current flow sheet as output at each level of the synthesis procedure. Also list the heuristics used at each step.