Question:

Identify the type of reaction:

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Addition of HX (like HBr) to alkenes generally follows electrophilic addition mechanism and Markovnikov’s rule.
Updated On: May 6, 2026
  • Electrophilic addition
  • Free radical substitution
  • Nucleophilic addition
  • Free radical addition
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The Correct Option is A

Solution and Explanation

Step 1: Identify the reactant.
The reactant is an alkene \( (CH_3-CH=CH_2) \) which contains a \( \pi \)-bond.

Step 2: Nature of alkene reaction.

Alkenes are electron-rich due to the \( \pi \)-bond, so they attract electrophiles.

Step 3: Identify reagent.

\( HBr \) provides \( H^+ \) (electrophile) and \( Br^- \).

Step 4: Mechanism.

First step: \( H^+ \) attacks the double bond forming a carbocation.
Second step: \( Br^- \) attacks the carbocation.

Step 5: Product formed.

Product is \( CH_3-CH(Br)-CH_3 \), following Markovnikov’s rule.

Step 6: Type of reaction.

Since electrophile adds across double bond, it is electrophilic addition.

Step 7: Final conclusion.

\[ \boxed{\text{Electrophilic addition}} \]
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