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Organic Synthesis

Esters, acyl chlorides, condensation polymers and racemic mixtures

  • 4 things to know
  • Components 02 and 03

Overview

Recall questions on forming an ester and an acyl chloride, the products with amines and alcohols, the monomers of polyesters and polyamides, and why HCN addition gives a racemic mixture.

What you need to know

Answer each one before you reveal it.

Your recallNot started
Key term

What monomers are required to form a polyamide by condensation polymerisation?

Key term

What product forms when an acyl chloride reacts with an amine?

Key term

What is produced when an acyl chloride reacts with an alcohol?

Key term

Why does nucleophilic addition of HCN to an aldehyde produce a racemic mixture?

Questions from this subtopic

Each one with the model answer underneath.

  1. 1

    What reagent reacts with a carboxylic acid to form an ester?

    Model answer

    An alcohol (in the presence of an acid catalyst).

  2. 2

    Name a reagent that converts a carboxylic acid into an acyl chloride.

    Model answer

    SOCl₂ (thionyl chloride) or PCl₅ (phosphorus pentachloride).

  3. 3

    What product forms when an acyl chloride reacts with an amine?

    Model answer

    An amide (and HCl).

  4. 4

    What is produced when an acyl chloride reacts with an alcohol?

    Model answer

    An ester (and HCl).

  5. 5

    Why might the order of steps in a synthetic route be important?

    Model answer

    To protect certain functional groups from unwanted reactions or to ensure selectivity of reactions.

  6. 6

    What monomers undergo condensation polymerisation to form a polyester?

    Model answer

    A dicarboxylic acid and a diol.

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AThe first step is Cl• + O₃ → ClO• + O₂.
BThe second step is ClO• + O → Cl• + O₂.
CThe overall equation is O₃ + O → 2O₂.

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In ClO⁻, chlorine has oxidation number +1.
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