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Polymers and Life

Optical isomerism

  • 2 things to know
  • Components 01, 02 and 03

Overview

Recall questions on what a chiral centre is, identifying one in a structure, why the isomers are drawn in three dimensions, and racemic mixtures.

What you need to know

Answer each one before you reveal it.

Your recallNot started
Process

How do you decide whether a carbon is a chiral centre, why must enantiomers be drawn three-dimensionally, and why does a laboratory synthesis give a racemic mixture?

Key term

Why is optical isomerism a form of stereoisomerism rather than structural isomerism?

Questions from this subtopic

Each one with the model answer underneath.

  1. 1

    What does it mean to describe a molecule as chiral?

    Model answer

    It means the molecule cannot be superimposed on its own mirror image.

  2. 2

    What is a chiral centre?

    Model answer

    It is a carbon atom that is bonded to four different atoms or groups.

  3. 3

    Define the term enantiomers.

    Model answer

    They are two forms of a compound that are non-superimposable mirror images of each other.

  4. 4

    How would you decide whether a given carbon atom in a structure is a chiral centre?

    Model answer

    Follow all four groups attached to it outwards and check that no two of them are identical.

  5. 5

    How is a chiral centre shown in a three-dimensional representation of a molecule?

    Model answer

    Two bonds are drawn in the plane of the paper, one as a solid wedge coming towards the viewer and one as a dashed wedge going away.

  6. 6

    Why must the two forms be drawn three-dimensionally rather than flat?

    Model answer

    Flat structures for the two enantiomers are identical, so the difference only appears once the arrangement in space is shown.

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