Web4. Cleaning Up Place your recovered materials in the appropriate labeled collection con-tainers as directed by your laboratory instructor. Clean your glassware with soap or detergent. Caution: Wash your hands thoroughly with soap or detergent be-fore leaving the laboratory. Post-Laboratory Questions 1. Calculate the percent yield of phenacetin … WebIn this experiment, you will attempt to brominate the phenacetin. Elemental bromine will not be used.Instead, bromine will be produced in the “pot” by reaction of hydrobromic acid with bromate ion (as shown below). This method is widely used for bromination of aromatics because it does not involve handling liquid bromine, which is quite corrosive.
Exp 5 Synthesis and Bromination of Phenacetin - StuDocu
WebCHEM 110L Spring 2024 - Remote Lab Performed by Daniel Droege & Christin Cudahy Directed / Led by Jerah Barnett University of California, Santa Cruz Web1. CHEM3412 Lab Synthesis of Benzocaine by Fischer Esterification. H 2 N. OH. O. EtOH H 2 N; OEt. O. H 2 O; H 2 SO 4 Benzocaine. Introduction Benzocaine is a local/topical anesthetic related to procaine (Novocain) and lidocaine. Benzocaine is the ethyl ester of para-aminobenzoic acid (PABA), a compound used in some sunscreens. firefly bray
4.9: Halogenation, Sulfonation, and Nitration of Aromatic …
WebInstead of using toxic bromine (Br2) as the brominating agent, a greener process will be utilizing HBr and H2O2. Write a balanced equation for this reaction 2 HBr (aq) + H2O2 (aq) --> Br2 (s) + 2H2o (l) Why is it important to add NaHCO3 slowly to the solution after the bromination is complete? Web1006 Bromination of 4-ethoxyacetanilide (phenacetin) to 3-bromo-4-ethoxyacetanilide Br HN O CH 3 O CH 3 HN O CH 3 O CH 3 KBrO 3, HBr acetic acid C 10H 13NO 2 C 10H 12BrNO 2 (179.2) (167.0) (80.9) (258.1) Literature P.F. Schatz, J. chem. Educ. 1996, 73, 267 Classification Reaction types and substance classes electrophilic substitution of ... WebWestern Kentucky University etf canada best 2022