Answer:
The alkene has Z configuration as shown in the figure.
The products of bromination of this compound are shown in the figure too with they stereochemistry.
Step-by-step explanation:
The cis/trans nomenclature system in alkenes is insufficient when there are three or more different substituents in the double bond. In these cases, the Z/E nomenclature system, adopted by IUPAC, is used for all alkenes. Z comes from the German word zusammen which means together and E from the German word entgegen which means opposite. They would be equivalent to the terms cis and trans respectively.
If a molecular configuration is Z or E is determined by the priority rules of Cahn, Ingold and Prelog. For each of the two carbon atoms of the double bond, it is determined individually which of the two substituents has the highest priority. If both substituents of higher priority are on the same side, the arrangement is Z. On the other hand, if they are on opposite sides, the arrangement is E.
Halogenation of alkenes
Takes place with the addition of halogen atoms to the double bond to give a neighborhood dihaloalkane.
Halogenation mechanism
Halogenations are carried out at room temperature and in inert solvents such as carbon tetrachloride. In the mechanism it is observed that the opening of the bromonium ion occurs on the opposite side to the positive bromine that is the leaving group, this causes the halogens to be anti in the final product.