Identify the major product (P) for the follow | vedclass

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(B) Step $1$: Dehalogenation with $Zn/\Delta$ removes the two bromine atoms to form a double bond, resulting in $3-	ext{ethyl}-4-	ext{methylcyclopen

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$1-$bromo$-1-$methyl$-2-$ethylcyclopentane

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(B) Step $1$: Dehalogenation with $Zn/\Delta$ removes the two bromine atoms to form a double bond, resulting in $3-	ext{ethyl}-4-	ext{methylcyclopentene}$.Step $2$: Electrophilic addition of $HBr$ to the alkene follows Markovnikov's rule. Protonation of the double bond forms a secondary carbocation.Step $3$: $A$ $1,2-	ext{hydride shift}$ occurs to form a more stable tertiary carbocation at the carbon bearing the methyl group.Step $4$: The bromide ion $(Br^-)$ attacks the tertiary carbocation to form $1-	ext{bromo}-1-	ext{methyl}-2-	ext{ethylcyclopentane}$ as the major product.

Identify the major product $(P)$ for the following reaction sequence:
$1,2-\text{dibromo}-3-\text{ethyl}-4-\text{methylcyclopentane} \xrightarrow[(ii) HBr]{(i) Zn, \Delta} (P)$

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Identify the major product $(P)$ for the following reaction sequence:$1,2-\text{dibromo}-3-\text{ethyl}-4-\text{methylcyclopentane} \xrightarrow[(ii) HBr]{(i) Zn, \Delta} (P)$