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Alcohols and Phenols

Reactions of primary and secondary alcohols

  • 3 things to know
  • A2 Unit 4

Overview

Recall questions on Reactions of primary and secondary alcohols.

What you need to know

Answer each one before you reveal it.

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Key term

Why is concentrated phosphoric acid, rather than concentrated sulfuric acid, used with potassium iodide to make an iodoalkane?

Key term

Place primary, secondary and tertiary alcohols in order of how readily they react with hydrogen halides.

Key term

What extra reagent helps a primary alcohol react with hydrochloric acid, in what order do the classes of alcohol react, and what forms when a primary alcohol meets ethanoyl chloride?

Questions from this subtopic

Each one with the model answer underneath.

  1. 1

    What type of compound is formed when an alcohol reacts with a hydrogen halide?

    Model answer

    A halogenoalkane, together with water. The hydroxyl group is replaced by the halogen atom, so ethanol and hydrogen bromide give bromoethane.

  2. 2

    Write the equation for the reaction of ethanol with hydrogen bromide.

    Model answer

    C₂H₅OH + HBr → C₂H₅Br + H₂O. The product is bromoethane and the reaction is a substitution.

  3. 3

    How is the hydrogen bromide usually supplied when a bromoalkane is prepared from an alcohol?

    Model answer

    It is generated in the flask by warming sodium bromide with concentrated sulfuric acid, NaBr + H₂SO₄ → NaHSO₄ + HBr, and the alcohol is present so that the hydrogen bromide reacts as it forms. The mixture is then heated under reflux.

  4. 4

    Why is concentrated phosphoric acid, rather than concentrated sulfuric acid, used with potassium iodide to make an iodoalkane?

    Model answer

    Concentrated sulfuric acid is a strong enough oxidising agent to oxidise iodide ions to iodine, so much of the halide would be destroyed before it could form hydrogen iodide. Phosphoric acid is not an oxidising agent, so it liberates hydrogen iodide cleanly.

  5. 5

    What extra reagent helps a primary alcohol react with concentrated hydrochloric acid?

    Model answer

    Anhydrous zinc chloride is added as a catalyst, and the mixture is warmed. Without it a primary alcohol reacts only very slowly with hydrogen chloride, whereas a tertiary alcohol reacts on shaking at room temperature.

  6. 6

    Place primary, secondary and tertiary alcohols in order of how readily they react with hydrogen halides.

    Model answer

    Tertiary reacts fastest, then secondary, then primary. The reaction proceeds most easily when the carbon bearing the hydroxyl group can support a positive charge, and alkyl groups attached to that carbon release electron density towards it, so more alkyl groups make substitution easier.

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