Reactions of cyclohexene's

Right got to hand this in tomorrow but I seem to be clueless can someone explain how to do this?
like the teacher is so ****ing **** I haven't got a clue what to do.
Thanks in advance

Right got to hand this in tomorrow but I seem to be clueless can someone explain how to do this?
like the teacher is so ****ing **** I haven't got a clue what to do.
Thanks in advance

Cyclohexene is a cycloalkene. Alkenes undergo electrophilic addition with Br2 forming two C-Br bonds where the alkene pi bond was. The mechanism is the same as any old electrophilic addition, you may have learnt it with a simple alkene such as ethene, the same principal applies here.

And the last part? C6H10 + H2SO4 --> ?
Right might be a stupid question how come cyclohexene doesn't go with the standard CnH2n and not C6H12?

As for the sulphuric acid question, any alkene that reacts with H2SO4 at high temperature and pressure is likely to undergo an acid catalysed hydration. This means that water is added across the double bond with the intermediate species being a cyclohexane with a sulphonate substituent. The end product of this is an alcohol hence you would form cyclohexanol as your final product.