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Carboxylic Acids MCQs

Carboxylic Acids MCQs are multiple-choice questions on the naming, structure, preparation and reactions of carboxylic acids and their conversion into acyl chlorides, anhydrides, esters and amides. They follow the MDCAT chemistry curriculum, and every question on MCQs360 shows its correct answer instantly so you can revise reagents and products with quick feedback.

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About Carboxylic Acids MCQs

Questions in this topic begin with IUPAC names such as propanoic acid and 2-methylpropanoic acid, the structure of the carboxyl group and preparation by oxidation or hydrolysis of nitriles. Acidity questions compare carboxylic acids with phenols and alcohols and include pH calculations for ethanoic acid from its Ka value. Reaction questions cover reduction with lithium aluminium hydride, decarboxylation of sodium ethanoate with soda lime, the formation of amides by heating ammonium salts and the conversion of acids into acyl chlorides, anhydrides and esters. You will also meet the hydrolysis of ethanoyl chloride and the alkaline hydrolysis of esters.

Key facts to remember

  • Carboxylic acids contain the –COOH group and are named with the suffix -oic acid, for example CH₃CH₂COOH is propanoic acid.
  • Ethanoic acid is a weak acid with Ka = 1.8 × 10⁻⁵ mol dm⁻³ (pKa 4.74); its anion is stabilised by resonance.
  • Carboxylic acids liberate CO₂ from sodium hydrogencarbonate, which distinguishes them from phenols.
  • SOCl₂, PCl₅ or PCl₃ convert a carboxylic acid into an acyl chloride, and heating with an alcohol and concentrated H₂SO₄ gives an ester.
  • Lithium aluminium hydride, LiAlH₄, reduces carboxylic acids to primary alcohols.
  • Heating sodium ethanoate with soda lime removes CO₂ and gives methane.

Exams that include Carboxylic Acids MCQs

Pakistan

  • MDCAT
  • ECAT
  • NUMS
  • AKU
  • FSc boards

India

  • NEET
  • JEE Main

Bangladesh

  • HSC
  • Medical Admission Test

How to prepare for Carboxylic Acids MCQs

  1. Draw a conversion map linking the acid to its acyl chloride, anhydride, ester and amide with the reagents on each arrow.
  2. Use pH = ½(pKa − log c) for quick weak acid pH calculations.
  3. Learn the reactivity order of acid derivatives: acyl chloride > anhydride > ester > amide.
  4. Remember that alkaline ester hydrolysis gives the carboxylate salt and an alcohol, not the free acid.

Frequently asked questions

What does the MDCAT syllabus include in Carboxylic Acids?

The PMDC MDCAT curriculum covers the nomenclature, structure and preparation of carboxylic acids, their reactivity and their conversion to acyl halides, anhydrides and esters, along with interconversions between these derivatives.

Which exams ask Carboxylic Acids MCQs?

Carboxylic acid questions appear in MDCAT, ECAT, NUMS and AKU entry tests and FSc board papers in Pakistan, in NEET and JEE Main in India, and in HSC and medical admission tests in Bangladesh.

Why are carboxylic acids stronger acids than alcohols?

When a carboxylic acid loses a proton, the negative charge on the carboxylate ion is shared equally between two oxygen atoms by resonance. The alkoxide ion from an alcohol has no such stabilisation, so carboxylic acids ionise more readily.

Last reviewed October 2026