Suggest a synthesis for the formation of 3-propyl-1-nitrobenzene from benzene.
Suggest a synthesis for the formation of 3-propyl-1-nitrobenzene from benzene.
Starting with benzene, derive a synthesis of 1-chloro-2-nitrobenzene Cl NO2 Starting with benzene, derive a synthesis of 1-chloro-2-nitrobenzene Cl NO2
Design a synthesis of 2-bromo-1-butyl-4-nitrobenzene from benzene. Br O2N
Please put all 6 steps. Design a synthesis of 2-bromo-1-chloro-4-nitrobenzene from benzene or any mono-substituted benzene. Cl Br benzene or any mono-substituted benzene NO2 Part 1 out of 6 Choose the best option for the immediate precursor to the target molecule. CI Br NO2
Design a synthesis for 1-bromo-4-methyl-2-nitrobenzene using benzene as the starting material. You can handwrite everything. Please show the structures of the intermediates after each step as well as the reagents used.
What is the IUPAC name for the following substituted benzene? NO2 O 3-ethyl-1-isopropyl-5-nitrobenzene 3-ethyl-5-isopropyl-1-nitrobenzene O 5-ethyl-3-isopropyl-1-nixobenzene l-ethyl-3-isopropyl-5-nitrobenzene O 5-ethyl-1-isopropyl-3-nitrobenzene
9. Suggest a synthesis for the formation of 4-chlorobenzoic acid from toluene. (9 points)
The synthesis of 3-ethylaniline from benzene The synthesis of 3-ethylaniline from benzene represents a common complex synthesis problem in organic chemistry. The target molecule has two new substituent groups with particular regiochemistry. Furthermore, there are limitations to the direct synthesis of the molecule due to peculiarities groups attached to the molecule Amino groups cannot be directly added to the ring middotAmino groups react strongly with Lewis acids forming a highly deactivated ring Friedel-Crafts reactions will not work on deactivated rings....
Design a synthesis for 1-bromo-4-methyl-2-nitrobenzene using benzene as the starting material. You can handwrite everything. Please show the structures of the intermediates after each step as well as the reagents used. (NOTE: you can NOT use Friedel-Craft alkylation after Nitration.) ALSO, Professor said: ch3Br/FeBr3 --> Br/FeBr2 --> HNO3/H2SO4 OR Br2/FeBr2 -> CheCL/ALCL3 -> HNO3/H2SO4 would NOT work. Hint: need protecting group
Write the mechanism for the formation of propyl acetate (from acetic acid and n-propyl acetate) (showing structures)
Suggest a suitable synthetic strategy for the transformation of 3-methyl-1-pentanol into propyl 3-methylpentanoate.