Alkene G undergoes a selective bromination reaction upontreatment with Br2 in dichloromethane solvent. Consider which faceof the alkene will undergo the initial bromination to form thebromonium ion intermediate and draw this intermediate. Thebromonium ion intermediate undergoes selective nucleophilic attackto afford the dibrominated product. Draw the structure of thisproduct. Draw a mechanism for the entire reaction from G to productvia the bromonium intermediate.
