Electrophilc Aromatic Substitution Bromination Br FeBr3
-electrophilic attack on aromatic ring -resonance structures stabalize intermediate -aromaticity is restored in the product
Chapters 14 and 15 Conjugation-multiple bonds that alternate with single bonds. Electrons are delocalized in these conjugated systems. In addition the -bonds must be coplanar to achieve orbital overlap to be considered conjugated.
Chapter 11 Nucleophilic substitution reactions SN2 reactions General SN2 mechanism Nu
pentavalent transition state H Nu Nu X
Bimolecular rate constant, means rate is dependent on concentration of nucleophile and electrophile. SN2 reactions always oc