If benzene comes up they might ask you about the structure, ie. delocalised pi-bonding electrons.
You probably do know about SN1 and SN2 but not the names (well, I was like that anyway). SN1 is Substitution, nucleophilic, uni-mollecular; SN2 is substitution, nucleophilic, bi-mollecular.
Take Haloalkanes (Halogenoalkanes) as an example, the mechanism for them forming an alcohol is either of these. In a primary haloalkane, SN2 will probably be favoured, as there is 'simultaneous' breaking and forming of bonds. In a tertiary haloalkane SN1 will likely be favoured, as in the first step only the haloalkane itself is involved, the more electronegative halogen more likely to leave a carbocation, as due to the 3 electron-releasing alkyl groups, the carbocation is more stable.
If you want I can draw a mechanism on SN1 and SN2 and put them up here for you. It might be unlikely they're on the synoptic, as unit 5 already had a carbocation stability question and SN2 mechanism. You never know though, seeing there was quite a lot of repition of organic on units 4 and 5.