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

7953 Views

See similar Chemistry A Level tutors

Related Chemistry A Level answers

All answers ▸

Draw the reaction mechanism for the formation of ethanol from bromoethane and water and name the mechanism.


What is a rate of reaction? How can we calculate the rate of reaction?


Calculate the standard enthalpy of combustion of a methane sample by using the standard enthalpies of formation.


What is chirality/optical isomerism?


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:

© 2025 by IXL Learning