CHM 1321 Lecture Notes - Lecture 34: Sodium Hydroxide, Acetyl Group, Aspirin

• School: University of Ottawa
• Department: Chemistry
• Course: CHM 1321
• Professor: Greg Flynn

Document Summary

Saponification of esters: provide names for the following compounds a) b) O: draw the structure corresponding to the following names: (e)-2-butenal, 2-ethenylcyclohexanone, 4-oxohexanal, the benzyl carbocation, 1-phenylethanone (acetophenone, give the product of the following reactions, explain, using a mechanism, why the product from parts i and ii are different. Explain: how could you synthesize the following deuterium-labeled compound from benzene (note: d2o is readily available)? (remember: d = 2h, an isotope of 1h) D: give the products of the following reactions: a) b) c) d) e) f) g) h) O: ch3ch2ch2li, et2o, nh4cl, h2o, ch3mgbr, et2o. Draw mechanisms for the reactions and explain why the product depends on the conditions. Explain by showing the reaction that would happen instead. Me: provide a mechanism and the product for the following reactions: Problem set 4: give a mechanism and product for each of the following reactions: Problem set 4: fill in the reagents required to accomplish the following transformations: