Explain why alkenes can have stereoisomers

"Stereo-" refers to 3D space, like with stereo sound involving sound from all directions.  The C=C double bond has no free rotation, as this would require breaking the pi bond, which is energetically unfavourable. This leads to the occurencce of stereoisomers whereby the constituents attached to the C=C can be in a different orientation in space, while maintaining the molecular formula. E (entgegen = german for opposite) and Z (zusammen = german for together) are the two isomers possible around a C=C. E is when the two largest constituents are across from each other ie bottom right and top left, and Z is when they are together ie bottom right and bottom left.  

KB
Answered by Kieran B. Chemistry tutor

3532 Views

See similar Chemistry A Level tutors

Related Chemistry A Level answers

All answers ▸

Explain the delocalised model of benzene, and hence why it is less reactive with electrophiles than cyclohexene


Why does a sample containing compounds with chiral carbons have no effect on plane polarised light?


Describe a two step reaction route that can convert 1-Butene (CH2CHCH2CH3) into a compound that is more soluble in water. Use mechanisms to aid your answer (HINT: one of the steps involves nucleophilic substitution)


Why is the first ionisation energy of Potassium less than Sodium?


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