What is the correct IUPAC name for the following compound? H. N. CH3 O A. N-benzyl-N-methylamine O B. N-phenyl-N-methylamine O C. 2-amino-1-methyl-2-phenylpropane O D. 1,1-dimethylaniline
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- based on this video: on Hinsberg Test Tests for Amines - MeitY OLabs (8.5min) https://www.youtube.com/watch?v=j5jgMUWri8U Write the reaction (two-step, in skeletal) of each test amine when tested in the Hinsberg Test.COMPLETE THE TWO REACTIONS BELOWIs the crude (non-crystallized) acetanilide pure? Why or why not? Is the crystallized acetanilide pure? Why or why not?
- as a follow-up question can explain this mechanismFrom benzene, organic compunds with 5 carbonw or less and any other inorganic compound you want. Synthesize the derivative for the naphthalene.Chemistry Please answer the following two questions. 1.) Why are functional group interconversions controversial? (double bonds into epoxide) 2.) Explain the clincal trials that happen for epoxide containing molecules
- When aspirin is made from acetic acid, the by product is H2O; when acetic anhydride 1Sused, the by-product is acetic acid. When acetyl chloride is used (see above), the by product is HC1. Which route should you use if you were working for Leica, a company that mass produces aspirin on a daily basis? Why?What is the Rf of your alcohol product B? Which fractions would you combine to isolate pure alcohol product B?Consider a mixture of the following molecules. Which molecule will be in the organic layer after treatment with excess acid (e.g. HCl)? Options: A B C D All of the above
- Chemistry Please help explain this textbook question: Although N, N -dimethylaniline is extremely reactive toward electrophilic aromatic substitution and is readily substituted by weak electrophiles, such as diazonium and nitronium ions, this reactivity is greatly diminished by the introduction of an alkyl substituent in an ortho position.What is the correct reaction scheme look like between acetic acid and 3-methylbutanol in the presence of sulfuric acid? Which image attached is the correct reaction scheme?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…