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

12895 Views

See similar Chemistry A Level tutors

Related Chemistry A Level answers

All answers ▸

How does the reactivity change down Group 1 elements, and why?


How would you synthesise an carboxylic acid just from a primary haloalkane like bromoethane?


Elements in the Periodic Table often show periodic trends. Describe and explain the periodic trend in atomic radius and electronegativity from Na to Cl.


What is the mechanism for nucleophilic addition reactions at carbonyls?


We're here to help

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

MyTutor is part of the IXL family of brands:

© 2026 by IXL Learning