Show how you would synthesize the following compound starting with acetylene and compounds containing no more than two carbon atoms as organic starting material. You may use any additional reagents you need
Show how you would synthesize the following compound starting with acetylene and compounds containing no more...
7. Synthesis Problem (15 points) Show how you would synthesize 3 of the 4 following compounds in one chemical reaction. You may use any starting material you wish and any organic and inorganic reagents. Clearly indicate which ones you want graded by circling the molecules н, осн, Br ОН
Determine a synthetic scheme that would synthesize the following compound from the indicated starting material. You may use any sources of carbon or reagents in the synthetic scheme. Br + Co, a
10-2 Using acetylene as the starting material, show how you would synthesize the following compounds а) b) but-2-yne с) d)
Show now you would synthesize the compounds listed in each set from the starting material given. You may use alcohol, alxene, alkyne that is four carbon atoms or less, any organic solvents necessary and in organic reagents as needed. It should take steps or less set 1 Starting with benzene, show how to make met a - biomobenzaldenyde met a- chloroaniline 1 - (4- nitiophenye) piopan - 1 - 01 1 - (3 - piopyephenye) piopan - 1 - 01...
9- Show how you would synthesize the following compound, beginning with 1-butene, Bromobenzene and any necessary additional reagents. More than one step is needed. 8 Br OH Bromobenzene, 1-Butene Show hew you weulel Syntfesige 4-Nonanone, begining witA 1-Butanol and any other non- oraanie reagents.(1-Butanol is the only Organic compeonn availabe)
S. Show how you would prepare the following compound using an organometallic reagent. You may use any hydrocarbons, organohalides, alcohols and/or carbonyl compounds that have five of fewer carbon atoms You may also use any needed reagents and solvents OH This one as well. He quits grading when you get two mistakes. 6. Propose a synthesis of the following compound using a Wittig reaction. You may use triphenylphosphine (Ph P) and any reagents containing five carbons or less as starting...
Starting with acetylene and bromoethane, show how you would use reagents from the table to synthesize 3,4-epoxyhexane. (Enter your choices as a string of letters without punctuation, i.e. ace.)
Starting with acetylene and bromoethane, show how you would use reagents from the table to synthesize meso-hexane-3, 4-diol. (Enter your choices as a string of letters without punctuation, i.e. ace.)
4. In each reaction show how you would synthesize the product from the reactant. Show the reagents, conditions, and the structures of any important intermediates along the way. Any organic reagent may be used, and more than one step may be used as well. Include mechanism (+-) H Br
8. Predict the number of peaks and the 'H splitting (multiplicity) for the following compound: он Outline the synthetic steps necessary to synthesize the compound below. You may use any organic or inorganic reagents you need but no more than 3 carbons starting compounds. Show the structures of all intermediate compounds that would probably be isolated during the course of your synthesis, and show all necessary reagents 9.