Identify the major product X in the following | vedclass

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(A) Step $1$: Protonation of the hydroxyl group gives $(CH_3)_3C-CH(OH_2^+)-CH_3$.Step $2$: Loss of water molecule forms a secondary carbocation: $(CH

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$2,3-	ext{dimethyl-2-butene}$

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(A) Step $1$: Protonation of the hydroxyl group gives $(CH_3)_3C-CH(OH_2^+)-CH_3$.Step $2$: Loss of water molecule forms a secondary carbocation: $(CH_3)_3C-CH^+-CH_3$.Step $3$: $A$ $1,2-	ext{methyl shift}$ occurs to form a more stable tertiary carbocation: $(CH_3)_2C^+-CH(CH_3)_2$.Step $4$: Elimination of a proton from the adjacent carbon atom yields the most stable alkene, $2,3-	ext{dimethyl-2-butene}$, according to $Zaitsev's$ rule.

Identify the major product $X$ in the following dehydration reaction: $(CH_3)_3C-CH(OH)-CH_3 \xrightarrow{H_2SO_4} X$.

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