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