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).

Answered by Labiba H. Chemistry tutor

5177 Views

See similar Chemistry A Level tutors

Related Chemistry A Level answers

All answers ▸

Describe, in three steps, how you would synthesise phenylethylamine (C6H5CH2CH2NH2) from methylbenzene, giving reagents and conditions for each step. For each step, state the type of reaction that occurs.


How does the mechanism for electrophilic addition work?


Describe the Kekule and delocalised model of benzene and explain some of the reasons why the kekule is disproved


You have 3.51g of hydrated zinc sulphate. You heat up the zinc sulphate until all the water has evaporated from it. The weight after heating is 1.97g. Find how many H2O molecules per zinc sulphate molecule there are in the hydrated form of it.


We're here to help

contact us iconContact usWhatsapp logoMessage us on Whatsapptelephone icon+44 (0) 203 773 6020
Facebook logoInstagram logoLinkedIn logo

© MyTutorWeb Ltd 2013–2024

Terms & Conditions|Privacy Policy