Edexcel International A Level (IAL) Chemistry (YCH11) - Unit 4 - 15.3 Optical activity-Study Notes - New Syllabus
Edexcel International A Level (IAL) Chemistry (YCH11) -Unit 4 – 15.3 Optical activity- Study Notes- New syllabus
Edexcel International A Level (IAL) Chemistry (YCH11) -Unit 4 – 15.3 Optical activity- Study Notes -International A Level (IAL) Chemistry (YCH11) – per latest Syllabus.
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Edexcel International A Level (IAL) Chemistry (YCH11) -Concise Summary Notes- All Topics
15.3 Optical Activity
Optical activity is a characteristic property of substances containing chiral molecules. A single optical isomer can rotate the plane of plane-polarised light, demonstrating the presence of chirality.
Definition of Optical Activity
Optical activity is the ability of a substance to rotate the plane of polarisation of plane-polarised monochromatic light.
Conditions for Optical Activity
- Molecule must contain a single chiral centre.
- Substance must contain only one enantiomer.
- Light used is:
- Plane-polarised
- Monochromatic (single wavelength)
Plane-Polarised Light
Normal light vibrates in many planes.
Plane-polarised light vibrates in: One plane only
Effect of Enantiomers
- One enantiomer rotates light clockwise.
- The other rotates light anticlockwise.
- Rotation occurs by the same angle but in opposite directions.
Terms Used
- Dextrorotatory (+): rotates light clockwise
- Laevorotatory (−): rotates light anticlockwise
Important Note
- Direction of rotation cannot be predicted from structure alone at this level.
- It must be determined experimentally.
Racemic Mixture
A 50:50 mixture of both enantiomers is called a:
Racemic mixture
It is optically inactive because:
- Equal and opposite rotations cancel each other.
Examples of Optically Active Compounds
- 2-butanol
- Lactic acid
- Amino acids (except glycine)
Key Features
- Optical activity results from chirality.
- Single enantiomers rotate plane-polarised light.
- Enantiomers rotate light equally but oppositely.
- Racemic mixtures are optically inactive.
Example 1:
Explain why a pure sample of one enantiomer is optically active.
▶️ Answer/Explanation
The molecule contains a chiral centre.
It rotates the plane of plane-polarised light in one direction.
Since only one enantiomer is present, the rotation is not cancelled.
Example 2:
Explain why a racemic mixture does not rotate plane-polarised light.
▶️ Answer/Explanation
A racemic mixture contains equal amounts of both enantiomers.
One rotates light clockwise and the other anticlockwise by the same angle.
The rotations cancel, so there is no overall rotation.
