Starting from benzene, acetone, acetaldehyde, cyclohexene, and methyl halides use common reagents to design syntheses for the following compounds. Any source of carbon in your product must be synthesized from these compounds.
Starting from benzene, acetone, acetaldehyde, cyclohexene, and methyl halides use common reagents to design syntheses for...
outline labratory syntheses of each of the following compounds starting with benzene and any other reagents Outline laboratory syntheses of each of the following compounds, starting with benzene and any other reagents. (c) CI (a) p-nitrotoluene (b) p-dibromobenzene (c) p-chloroacetophenone (d) m-nitrobenzenesulfonic acid (e) p-chloronitrobenzene (f) 1,3,5-trinitrobenzene (g) 2,6-dibromo-4-nitrotoluene
Synthesis Experiment #2: Design syntheses to produce the following compounds starting with ethylene and any methyl halide. Note that once a compound has been synthesized in one process it can be used in a different process if you reference where it was first made.
Propose syntheses of the following molecules, starting from benzene, toluene or phenol, any inorganic reagents and any organic reagent of TWO carbons or less: 4. Propose syntheses of the following molecules, starting from benzene, toluene or phenol, any inorganic reagents and any organi c reagent of TWO carbons or le a) NO2 b) CO2H c) OH d) e) NO2 NO2 Br CI CI CO2H Br
(14) V. Starting from benzene and any other reagents you need, propose an efficient synthesis of th following compound. (10) VI. Devise a synthesis that will accomplish the following transformation in good yield. Use the given compounds as the only organic source of carbon atoms. You may use any common organic solvents as well as any needed inorganic reagents (14) V. Starting from benzene and any other reagents you need, propose an efficient synthesis of th following compound. (10) VI....
Design an effective synthesis for each of the following amino acids starting from the compounds shown on the left. You may also use any monofunctional organic compound containing four or less carbon atoms, and any inorganic reagents in your syntheses.
Design syntheses to produce the following compounds starting withany alkyl halide with 3 or fewer carbons and butadiene. You may useany any inorganic reagents necessary. Note that once a compound hasbeen synthesized in one process it can be used in a different process ifyou reference where it was first made.
2. Design multi-step syntheses for TWO of the following targets. Show the reagents needed for each step and the product of each step. Special conditions: You must use cyclopentadiene as your starting material for all syntheses. You may use organic reagents containing 4 or fewer carbons, and any inorganic reagents. For any Diels-Alder reaction that you use (necessary for all targets!), the dienophile must be an a,ß-unsaturated carbonyl compound. Target 1: HO D Target 2: Doe Target 3: ro Target...
6. Starting with benzene and using any other necessary reagents of your choice, design a synthesis for the following compound. Note: there may be more than one plausible answer 7. Starting with benzene and using any other necessary reagents of your choice, design a synthesis for the following compound. Note: there may be more than one plausible answer 8. Starting with benene and using any other necessary reagents of your choice, design a synthesis for the following compound. Note: there...
Devise a synthesis of these compounds starting with 3-carbon alkyl halides. Show any necessary reagents and reaction conditions. All carbons must ultimately come from the 3-carbon alkyl halides. Once you have made a new compound, you may reuse it without making it again. a) Propanone b) Butanoic acid c) 3-hexene
Name 4. Starting with cyclohexene and acetylene as the only source of carbons, show a synthesis of the compound below. 1. Show how you could make the given product from the given starting material. Show all steps. OH a CECH 2. Starting with acetylene and methyl bromide as your only source of carbons show a synthesis of cis-2-butene. 5. Prepare 2-methoxy-propanol from 1-bromo-propane. Show the steps and use any reagents you need. 3. Using acetylene and propyl bromide as your...