Step 1: General chemical equation.
Acid-catalysed hydration of alkenes follows Markovnikov’s rule. Example with ethene:
\[
CH_2 = CH_2 + H_2O \;\xrightarrow{H_2SO_4}\; CH_3CH_2OH
\]
Step 2: Mechanism.
\begin{enumerate}
\item
Protonation of alkene:
\[
CH_2 = CH_2 + H^+ \;\longrightarrow\; CH_3-CH_2^+
\]
(formation of carbocation)
\item
Nucleophilic attack by water:
\[
CH_3-CH_2^+ + H_2O \;\longrightarrow\; CH_3-CH_2OH_2^+
\]
\item
Deprotonation:
\[
CH_3-CH_2OH_2^+ \;\longrightarrow\; CH_3-CH_2OH + H^+
\]
\end{enumerate}
Conclusion:
The final product is an alcohol, and the reaction is catalysed by an acid (usually \(H_2SO_4\)).