Markovnikov Rule

Electrophilic Addition: The reaction begins with the attack of the $π$ -bond on the proton ( $H^{+}$ ) of $H B r$ .
Markovnikov's Rule: The proton adds to the carbon atom that already has more hydrogen atoms (the terminal $C H_{2}$ group).
Carbocation Intermediate: This results in the formation of a Secondary Carbocation ( $C H_{3} - C H^{+} - C H_{3}$ ), which is more stable than a primary one.
Nucleophilic Attack: The bromide ion ( $B r^{-}$ ) then attacks the positively charged secondary carbon.
Final Product: 2-Bromopropane is formed as the major product.

This easy difficulty chemistry question is from the chapter hydrocarbons, covering the topic of markovnikov rule. It appeared in the 2025 exam.

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Markovnikov Rule

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A hydrocarbon with the molecular formula $C_{6} H_{10}$ is being analysed, and the total number of degr...