Answer:
3-bromobenzoic acid
Explanation:
In this case, we have to remember that the Br_2/FeBr_3 is a reaction in which we add Br into the molecule an electrophilic aromatic substitution. Additionally, we have a carboxylic acid in the benzene. This carboxylic acid is an ortho director because is a deactivating group (it removes electrons from the benzene ring). With this in mind, a "Br" atom would be added in an ortho position respect to the COOH group and we will obtain 3-bromobenzoic acid.
See figure 1.
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