(a) Ethanol under high pressure and low temperature when treated with oxidising agent like acidified potassium dichromate produces ethanoic acid (acetic acid).
C 2 H 5 OH ethanol[ethyl alcohol] → K 2 Cr 2 O 7 [O] CH 3 CHO ethanal [acetaldehyde] → K 2 Cr 2 O 7 [O] CH 3 COOH ethanoic acid[acetic acid] \underset{ \text{ ethanol[ethyl alcohol]}}{\text{C}_2\text{H}_5\text{OH}} \xrightarrow[\text{K}_2\text{Cr}_2\text{O}_7]{\text{[O]}} \underset{\text{ethanal [acetaldehyde] }}{\text{CH}_3\text{CHO}} \xrightarrow[\text{K}_2\text{Cr}_2\text{O}_7]{\text{[O]}} \underset{ \text{ethanoic acid[acetic acid]} }{\text{CH}_3\text{COOH}} ethanol[ethyl alcohol] C 2 H 5 OH [O] K 2 Cr 2 O 7 ethanal [acetaldehyde] CH 3 CHO [O] K 2 Cr 2 O 7 ethanoic acid[acetic acid] CH 3 COOH
(b) Acetylene is first converted to acetaldehyde by passing it through a 40 percent H2 SO4 solution at 60°C in the presence of 1% Mercury(II) Sulphate [HgSO4 ].
C 2 H 2 acetylene + H 2 O → H 2 SO 4 (dil) , HgSO 4 CH 3 CHO ethanal [acetaldehyde] \underset{\text{acetylene}}{\text{C}_2\text{H}_2} + \text{H}_2\text{O} \xrightarrow{\text{H}_2\text{SO}_4\text{(dil) , HgSO}_4}\underset{\text{ethanal [acetaldehyde] }}{\text{CH}_3\text{CHO}} acetylene C 2 H 2 + H 2 O H 2 SO 4 (dil) , HgSO 4 ethanal [acetaldehyde] CH 3 CHO
The acetaldehyde is oxidised to acetic acid by passsing a mixture of acetaldehyde vapous and air over manganese acetate at 70°C
2 CH 3 CHO ethanal [acetaldehyde] + O 2 → Catalyst Δ 2 CH 3 COOH ethanoic acid[acetic acid] \underset{\text{ethanal [acetaldehyde] }}{2\text{CH}_3\text{CHO}} + \text{O}_2 \xrightarrow[\text{Catalyst}]{\Delta} \underset{ \text{ethanoic acid[acetic acid]} }{2\text{CH}_3\text{COOH}} ethanal [acetaldehyde] 2 CH 3 CHO + O 2 Δ Catalyst ethanoic acid[acetic acid] 2 CH 3 COOH