1.3. Propose a synthetic method from benzene the following molecule. NO Give the major product(s) of the following reactions. FeBr3 Br2 NO2 AIC3 CH,CI OCH3 AlCl, CH;CI OCH3 FeBr Br2
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- For butenafine, develop a synthesis that starts with napthalene and benzene. (aromatic methyl groups can be converted to alkyl bromides using Br2/light, and aldehydes by heating the alkyl bromide in DMSO, eg. ArCH3 to ArCH2Br then to ArCHO).Propose a mechanism for the followingreaction.Answer in 2 sig figs, thank you!
- Propose a structure consistent with each set of data.plz provide DETAILED written explanation and AVOID USING MECHANISMS.Fast pls in 5 min will give u like for sure Create a synthesis of the heterocyclic compound 5 from starting materials each containing no more than six carbon atoms.In the solution you should use retrosynthetic analysis to justify your choice.
- Given this organic synthesis, is there any limiting and excess reagents? also describe the procedure is run, how is the reaction monitored?Is the order fo addition important? N-ETHYLALLENIMINE[Aziridine, 1-ethyl-2-methylene-] Submitted by Albert T. Bottini and Robert E. Olsen1.Checked by Thomas H. Lowry and E. J. Corey. 1. ProcedureCaution! This preparation should be carried out in a good hood to avoid exposure to ammonia. The operator should wear rubber gloves and protective goggles because 2-haloallylamines and ethylenimines can cause severe skin and eye irritation. A 2-l. three-necked flask is fitted with a sealed mechanical stirrer, a gas-inlet tube, and a dry ice condenser protected from the air by a soda-lime drying tube (Note 1). The system is flushed thoroughly with dry ammonia, and 32.8 g. (0.84 mole) of sodium amide (Note 2) is added to the flask. The system is again flushed with ammonia, the condenser is provided with dry ice covered by acetone, and 1.2 l. of liquid…Synthesize 3,5-dibromotoluene from benzene and any suitable inorganic and organic reagents. Assume you CANNOT separate ortho and para products and both isomers have to be carried through in the entire synthesis.Cleavage of oct-1-ene with hot, KMnO4 will yield _____________. octanol and carbon dioxide octanone hexanol and 2 carbon dioxides heptanal and formaldehyde heptanoic acid and carbon dioxide