Explain, why the reaction of m-bromoanisole with sodamide gives only one product. b) Describe the bromination reactions at allylic and benzylic positions by N-bromosuccinimide.

The reaction of m-bromoanisole with sodamide gives only one product due to the specific nature of the reaction mechanism. Sodamide (NaNH₂) is a strong base that induces elimination of the proton from the carbon adjacent to the bromine atom in m-bromoanisole. In this case, the elimination leads to the formation of an aryl anion intermediate, which ___ _______ _____ ______ ______ ______ __________ ______ ______.
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