An aldehyde CH3CH2CH2CHO reacts with potassium cyanide (KCN) to form a racemic mixture of two stereoisomers of CH3CH2CH2CH(OH)CN. A)Explain why a racemic mixture is formed and b)describe how you would distinguish between 2 samples of the stereoisomers

A) The aldehyde contains a planar carbon group which can be attacked from both sides. Each side has equal probability of being attacked resulting in a racemic compound containing equal amounts of each stereoisomer.B) Shine plane polarised light on the compounds, each will rotate light in opposite directions.

IW
Answered by Isobel W. Chemistry tutor

8216 Views

See similar Chemistry A Level tutors

Related Chemistry A Level answers

All answers ▸

Why is there a difference in mechanism between tertiary halogenoalkanes and primary halogenoalkanes in nucleophilic substitution?


Why is methylamine a stronger base than phenylamine?


State why it is initially unexpected for alkenes to undergo electrophilic addition with bromine. Explain why this reaction does indeed occur.


Why do we use the n+1 rule in proton NMR?


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