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Q. Consider the following reaction.
$H_3C - \underset{\underset{D}{|}}{CH} - \underset{\underset{CH_3}{|}}{CH} - CH_3 Br ^• \to X +HBr$
Identify the structure of the major product $X$.

Haloalkanes and Haloarenes

Solution:

$CH_3 - \underset{\underset{D}{|}}{CH} - \underset{\underset{CH_3}{|}}{\overset{•}{C}} - CH_3 $ is the tertiary free radical

which is the most stable amongst the given options.