(i) Compound 'X' is Ethanoic acid (CH₃COOH).
Structure:
$$\text{CH}_3 - \text{COOH}$$
(Two carbon atoms: a methyl group attached to a carboxyl group –COOH)
(ii) Ethanoic acid is a weak acid — it does not ionise completely in water, so its pH is higher (less acidic) than a mineral acid like HCl or H₂SO₄, which are strong acids and ionise completely, giving a much lower pH.
(iii) The reaction is called Esterification. When ethanoic acid reacts with ethanol (in the presence of conc. H₂SO₄), a sweet-smelling ester is formed:
$$\text{CH}_3\text{COOH} + \text{C}_2\text{H}_5\text{OH} \xrightarrow{\text{conc. H}_2\text{SO}_4} \text{CH}_3\text{COOC}_2\text{H}_5 + \text{H}_2\text{O}$$
(Ethyl ethanoate is the ester produced.)
(iv) The salt produced is Sodium ethanoate (CH₃COONa). The gas evolved is CO₂.
$$2\text{CH}_3\text{COOH} + \text{Na}_2\text{CO}_3 \rightarrow 2\text{CH}_3\text{COONa} + \text{H}_2\text{O} + \text{CO}_2\uparrow$$
Source: Carbon and its Compounds, Sections 4.3.2–4.3.3
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