Consider the following reaction:H_3C-CH(D)-CH | vedclass

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(B) The reaction involves the abstraction of a hydrogen atom by a bromine radical $(Br^\bullet)$.The stability of the resulting alkyl radical determin

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$H_3C-CH(D)-C^\bullet(CH_3)-CH_3$

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(B) The reaction involves the abstraction of a hydrogen atom by a bromine radical $(Br^\bullet)$.The stability of the resulting alkyl radical determines the major product.The starting material is $2-deuterio-3-methylbutane$.Abstraction of a hydrogen atom from the $C-3$ position leads to a tertiary $(3^\circ)$ radical,which is more stable than a secondary $(2^\circ)$ or primary $(1^\circ)$ radical.Structure $B$ represents the radical formed at the $C-3$ position: $H_3C-CH(D)-C^\bullet(CH_3)-CH_3$.

Consider the following reaction:
$H_3C-CH(D)-CH(CH_3)-CH_3 + Br^\bullet \to X + HBr$
Identify the structure of the major product $X$.

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Consider the following reaction:$H_3C-CH(D)-CH(CH_3)-CH_3 + Br^\bullet \to X + HBr$Identify the structure of the major product $X$.