you are asked to prepared 1-bromo-2,2,3,3-tetramethlylbuane by
exposure to 2,2,3,3-tetramethylbutane to Br2 in the presence of
light....
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you are asked to prepared 1-bromo-2,2,3,3-tetramethlylbuane byexposure to 2,2,3,3-tetramethylbutane to Br2 in the presence oflight. How can yield of this monobrominated product be maximizedwhile minimazing the formation of polybrominated product?
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Answer Treatment of alkanes with Br2 in presence of light is the radical substitution of RH that generates the alkyl bromide and HBr is that the desired product in this case CH3CCH32CCH32CH2Br may be
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