CHM 1321 Lecture Notes - Lecture 19: Benzene, Reaction Mechanism, Electrophile

• School: University of Ottawa
• Department: Chemistry
• Course: CHM 1321
• Professor: Kathy Focsaneanu

Document Summary

Diference between aromaic, ani-aromaic or nonaromaic and draw the lcao orbital diagram of the pi bond system. Label lone pairs, formal charges and electron pushing arrows to complete reacion mechanisms. Idenifying the most acidic proton in a molecule and staing its pka value. Be able to take a reacion and develop its mechanism be able to indicate any stereochemistry. Be able to draw chair conformers of products and idenify which chair is the stable conformer. Be able to idenify which is part of the free radical chain reacion in an elementary step. Be able to draw mechanisms, and products of elementary steps, name the type of reacions and give 2 reasons why the regioselecivity of the product sterics and resonance. Be able to deine the reason for compunds as apart of catalyic reacions. Draw products and indicate which is the major product and the minor and why they do not form equal amounts.