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Draw the major product(s) from addition of HBr to the alkene below. . You do not have to consider stereochemistry. . If there is more than one major product possible, draw all of them. . Draw one structure per sketcher. Add additional sketchers using the . Separate multiple products using the + sign from the dropdown menu

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An example of an addition reaction is the hydrohalogenation of alkenes. Alkyl halides are produced when alkenes are hydrohalogenated. For instance, 2-bromopentane is produced when HBr and 1-pentene react.

Step 1: A tertiary carbocation intermediate is generated when the alkene is protonated.

Step 2: Alkyl bromide is produced when the bromide nucleophile attacks the carbocation intermediate in a nucleophilic manner.

This response observes Markovnikov'v guideline.

The electrophilic addition of hydrohalic acids like hydrogen chloride or hydrogen bromide to alkenes to produce the corresponding haloalkanes is known as a hydrohalogenation reaction.

The H + particle is drawn to the π‐bond electrons of the alkene, which frames a π complex. The complex then breaks, forming a single bond between the hydrogen and one of the double-bonded carbons. A carbocation is formed when a carbon atom loses some of its share of the bond.

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