What will be the major product in the followi | vedclass

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(C) The reactant is $1$-bromo-$2$-methylpropane,which is a primary alkyl halide with steric hindrance at the $\beta$-carbon.When treated with a strong

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$CH_3-C(CH_3)=CH_2$

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(C) The reactant is $1$-bromo-$2$-methylpropane,which is a primary alkyl halide with steric hindrance at the $\beta$-carbon.When treated with a strong base like methoxide $(CH_3O^-)$ in methanol $(CH_3OH)$,the reaction proceeds via an $E_2$ elimination mechanism rather than $S_N2$ substitution due to the bulky nature of the base and the structure of the substrate.The elimination of $HBr$ from the substrate leads to the formation of $2$-methylpropene as the major product.Reaction: $CH_3-CH(CH_3)-CH_2Br + CH_3O^- \rightarrow CH_3-C(CH_3)=CH_2 + CH_3OH + Br^-$

What will be the major product in the following reaction?
$CH_3-C(CH_3)(H)-CH_2Br \xrightarrow{CH_3O^- / CH_3OH}$

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What will be the major product in the following reaction?$CH_3-C(CH_3)(H)-CH_2Br \xrightarrow{CH_3O^- / CH_3OH}$