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