Stereoisomers and Stereodescriptors | How to Assign R and S Stereodescriptors | CIP Rules

[@nasooochemical3147]

Thank you very much for your presence 😊❤

[@akshadnimbarte]

Now this is what I really needed

[@VictortheOrganicChemistryTutor]

Glad it helps 😁

[@samoyedand2huskies]

I loveee your videos!!!! Thank you so much for helping me love orgo!!!!

[@VictortheOrganicChemistryTutor]

Thanks a ton! So happy you’re vibing with the orgo content! Keep on loving it!

[@eman4159]

Brilliant ! Thank youuu

[@VictortheOrganicChemistryTutor]

You're welcome!

[@ludovicaditucci87]

why doesn't this have many more views? great vid. thanks!

[@VictortheOrganicChemistryTutor]

Thanks to your comment, I’ll get a few more now 😅

[@longlifelearner2005]

This is just incredible, thank you alot!!!!

[@VictortheOrganicChemistryTutor]

You're very welcome!

[@sakacibiri]

thanks a lot

[@VvVv-x2u]

Sir I have a doubt why can't we keep lowest priority on wedge ,, are we changing the wedge and dash by rotating the molecule ??

[@VictortheOrganicChemistryTutor]

That’s precisely the point. In order to assign the stereodescriptor, the lowest priority group must be looking away from the observer.

[@eman4159]

Can you tell me the meaning of non superimposable?

[@VictortheOrganicChemistryTutor]

It’s when two objects are not the same no matter how much you rotate them in space.