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9701 · 29.4

Isomerism: optical

Some molecules exist as a pair of 'left-handed' and 'right-handed' versions, known as enantiomers. They are mirror images of each other but cannot be perfectly overlapped, just like your hands.

Need to know

What you need to know

  • Chirality: The property of a molecule being non-superimposable on its mirror image.
  • Chiral Centre: A carbon atom bonded to four distinct groups.
  • Achiral: A molecule that *is* superimposable on its mirror image. It will have a plane of symmetry.

Explanation

Mirror Image Molecules

  1. Chiral centre: carbon with four different groups. | Sim hint: Asymmetric carbon — no plane of symmetry.
  2. Enantiomers are non-superimposable mirror images. | Sim hint: Rotate molecule — cannot align all groups.
  3. Optical activity — rotate plane-polarised light. | Sim hint: Racemic mixture: equal enantiomers — no net rotation.
  4. Biological significance — enzyme stereospecificity. | Sim hint: One enantiomer active, other inert/harmful.