Question: When toluene is treated with bromine the bromine does react with the double bond to form a viscinal dihalide, but instead a substitution of one

When toluene is treated with bromine the bromine does react with the double bond to form a viscinal dihalide, but instead a substitution of one of the benzylic hydrogens takes places. Why?

When tolucne is treated with bromine (shown below), the bromine doesn't read doable bond to form a viscinal dihalide, but instead a substitution of one of the bydrogens takes place. Why? NOT FORMED Major Product

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