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9701 · 33.1

Carboxylic acids flashcards

Revision flashcards for Cambridge 9701 Carboxylic acids (syllabus 33.1). Flip, recall, then mark a real past-paper question.

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    What is the functional group of a carboxylic acid?

    The carboxyl group, written as –COOH. It consists of a carbonyl group (C=O) and a hydroxyl group (–OH) attached to the same carbon atom.

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    Why do carboxylic acids have higher boiling points than alcohols of similar molar mass?

    Carboxylic acids can form dimers through hydrogen bonding. Each molecule forms two hydrogen bonds with a neighbour, requiring more energy to separate the molecules and vaporise the liquid.

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    What is a dimer?

    A molecule made of two identical smaller molecules (monomers) linked together. In the case of carboxylic acids, two molecules are held together by two hydrogen bonds.

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    Are carboxylic acids strong or weak acids? Explain.

    They are weak acids. They only partially dissociate (ionise) in aqueous solution to release H⁺ ions, establishing an equilibrium. `RCOOH(aq) ⇌ RCOO⁻(aq) + H⁺(aq)`.

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    What is the standard test for a carboxylic acid?

    Add a small amount of sodium carbonate (Na₂CO₃) or sodium hydrogencarbonate (NaHCO₃). Effervescence (fizzing) will be observed as carbon dioxide gas is produced. This test distinguishes them from less acidic phenols.

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    What are the products of the reaction between ethanoic acid and magnesium?

    Magnesium ethanoate and hydrogen gas. `Mg(s) + 2CH₃COOH(aq) → (CH₃COO)₂Mg(aq) + H₂(g)`.

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    What type of reaction occurs between a carboxylic acid and an alkali like NaOH?

    A neutralisation reaction, forming a salt and water. For example, `CH₃COOH + NaOH → CH₃COONa + H₂O`.

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    What reagent is used to reduce a carboxylic acid to a primary alcohol?

    Lithium tetrahydridoaluminate, `LiAlH₄`, in dry ether, followed by aqueous workup. This is a powerful reducing agent.

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    Why is `NaBH₄` (sodium tetrahydridoborate) not used to reduce carboxylic acids?

    `NaBH₄` is a milder reducing agent and is not powerful enough to reduce the carboxyl group. It can, however, reduce aldehydes and ketones.

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    How can ethanoic acid be formed from ethanol?

    By oxidation using a strong oxidising agent, such as acidified potassium manganate(VII) (`KMnO₄/H⁺`) or acidified potassium dichromate(VI) (`K₂Cr₂O₇/H⁺`), under reflux.

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    What is the name of the salt formed from propanoic acid and potassium hydroxide?

    Potassium propanoate.