Carboxylic acids are identified by their acidity. They are weak acids, but strong enough to react with carbonates and release carbon dioxide.Method: add aqueous sodium carbonate (or sodium hydrogencarbonate, or solid carbonate) to the sample.• Positive result: effervescence (fizzing).
• Bubble the gas through limewater: it turns milky (cloudy), confirming CO2.With ethanoic acid:2CH3COOH + Na2CO3 → 2CH3COONa + H2O + CO2 The salt formed is sodium ethanoate. The ionic equation is the same for any carboxylic acid:2H+ + CO32− → H2O + CO2 Why this test is useful: phenols and alcohols are too weakly acidic to react with carbonates, so only the carboxylic acid fizzes. This makes the carbonate test a way to distinguish a carboxylic acid from a phenol.Worked example: how many moles of CO2 form when 0.020 mol of propanoic acid reacts with excess sodium carbonate?
From the equation, 2 mol acid gives 1 mol CO2.
So 0.020 mol acid gives 0.020 ÷ 2 = 0.010 mol CO2.The same reaction happens with metal carbonates such as CaCO3, and carboxylic acids also react with reactive metals (giving H2) and with bases.
• Bubble the gas through limewater: it turns milky (cloudy), confirming CO2.With ethanoic acid:
From the equation, 2 mol acid gives 1 mol CO2.
So 0.020 mol acid gives 0.020 ÷ 2 = 0.010 mol CO2.The same reaction happens with metal carbonates such as CaCO3, and carboxylic acids also react with reactive metals (giving H2) and with bases.