What is a racemic mixture and why is it not optically active?

A racemic mixture contains a 50-50 mixture of two optical isomers. Optical isomers are identical in molecular structure but rotate the plane of polarized light in different directions (one rotates clockwise, the other anticlockwise).As a racemic mixture contains an equal amount of both isomers, they cancel out each other's effect on light and the mixture is notoptically active as a result. An example of this is the formation of the two isomers of 2-hydroxypropanoic acid from ethanal (which can be shows on a whiteboard).

LH
Answered by Labiba H. Chemistry tutor

10452 Views

See similar Chemistry A Level tutors

Related Chemistry A Level answers

All answers ▸

What is the geometry of a ClF3 molecule? (AQA Unit 1 2015 1d)


What is meant by terms 'saturated' and 'unsaturated' when applied to alkanes and alkenes? Describe a chemical test to distinguish between the liquids hexane and hexene.


State how you would test a solution for the presence of sulfate ions? Explain, using an ionic equation, what you would expect to observe in the presence of sulfate ions.


Unsaturated fats change bromine water from orange to colourless. How?


We're here to help

contact us iconContact ustelephone icon+44 (0) 203 773 6020
Facebook logoInstagram logoLinkedIn logo

© MyTutorWeb Ltd 2013–2025

Terms & Conditions|Privacy Policy
Cookie Preferences