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In part B, the bromine in diethyl ether reacts with cyclohexene to produce 1,2dibromocyclohexane. This reaction is known as halogenations which involved the addition of
halogen, bromine in this case, to the carbon atom with the double bond (C=C). In both dark and
light surrounding, the reaction of bromine in diethyl ether with cyclohexene can be occurred
spontaneously is because the cyclohexene molecules contain a double bond between two carbon
atoms. In this case, cyclohexene behave as nucleophiles (Lewis base) in polar reaction, donating a
pair of electrons from their electron-rich C=C bond to bromine which is the electrophile.