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.

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