Starting with benzene, propose appopriate reagents to form the following compounds na te Starting wI ventenes,...
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
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
9. Propose an efficient synthesis of each molecule below starting from benzene and any other reagents needed (organic or inorganic) A. CI B. CI NO2 Br
(4pts) Propose a synthetic scheme from benzene and any other organic or inorganic reagents for the following compounds. a. COOH ci SOH NH2
37 Propose syntheses of the following compounds beginning from a mono- substituted benzene NH₂ CN b) CH₃ CH₂ CH₂ COH Br c) d) CI NH2
Question Propose syntheses of the following compounds beginning from a mono-substituted benzene. NH CH CN CH.CH ÇO,H NH Br o CI
Using the reagents list below, propose a synthesis of the target compound starting from benzene. Enter your answers as a list of letters corresponding to the selected reagents in order you wish to use them. You may assume that all reactions are appropriately worked up and that mixtures of comstitutional isomers can be separated Remaining Time: 59 minutes, 08 seconds. Question Completion Status: Moving to another question will save this response. Question 1 Using the reagents listed below, propose a...
Using the reagents listed below, propose a synthesis of the target compound starting from benzene. Assume all reactions are appropriately worked up and that mixture of constitutional isomers can be separated. CI NH2 A. Cl/FeCl3 B. HNO3/H2SO4 C. CH3COCI/AICI: D. NaNO2/HCI E. HC1/Cuci F. KCN/CuCN G. H3PO2 H. H2O/heat I. H Cr04 J. 1)LiAlH4 2)H20 K. H/Ni L. 1) Mg 2)CO2 3)H30 M. CH3OH/H30+ N. (CH3)2SO4 NaOH O. CH3OH SOCI Q. HCI R. NaN3
(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....
Starting with benzene and using any other neccessary reagents of your choice, design a synthesis for each of the following: OMe COOH Br Br NO NO (b) COOH NH Cl Cl NO2 COOH NO2 Cl NO Cl Br OEt NO2 Cl (h) C (g) NO2 Br O2N