Part 1: Two methods of preparation of monohydric alcohol.
Method 1: By hydration of alkenes.
Ethene reacts with water in presence of conc. H$_2$SO$_4$ or phosphoric acid catalyst to give ethanol:
\[
CH_2=CH_2 + H_2O \;\xrightarrow{H_2SO_4}\; CH_3CH_2OH
\]
Method 2: By reduction of aldehydes.
Acetaldehyde on reduction with hydrogen gives ethanol:
\[
CH_3CHO + H_2 \;\xrightarrow{Ni/Pt}\; CH_3CH_2OH
\]
Part 2: Reactions of ethyl alcohol with conc. H$_2$SO$_4$ at different temperatures.
(i) At 443 K (140$^\circ$C): Formation of diethyl ether.
\[
C_2H_5OH + C_2H_5OH \;\xrightarrow[443K]{conc. H_2SO_4}\; C_2H_5OC_2H_5 + H_2O
\]
(ii) At 443–463 K: Dehydration to form ethene.
\[
C_2H_5OH \;\xrightarrow[443-463K]{conc. H_2SO_4}\; CH_2=CH_2 + H_2O
\]
(iii) As oxidising agent: Formation of acetaldehyde.
\[
CH_3CH_2OH \;\xrightarrow{conc. H_2SO_4}\; CH_3CHO + H_2
\]
Conclusion:
Monohydric alcohols can be prepared by hydration of alkenes or reduction of aldehydes. Ethanol reacts with conc. H$_2$SO$_4$ differently depending on temperature, giving ether, ethene, or acetaldehyde.