Stereoisomers and Stereodescriptors | How to Assign R and S Stereodescriptors | CIP Rules
In this video we'll go over the two types of the stereoisomers: enantiomers and diastereomers, and talk about the CIP rules for the R and S stereodescriptors.
#organicchemistry #organicchemistrytutor #stereochemistry
00:00 Types of Isomers
02:34 What is Non-Superimposable
03:21 Enantiomers
05:14 Diastereomers
06:10 Stereoisomerism Recap
07:09 Stereodescriptors
08:10 CIP Rules for the R and S Stereodescriptors
19:49 Example 1
21:42 Example 2
24:08 Example 3 -- Double Flip Trick
28:15 Example 4 -- Using the Double Flip Trick Again
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Пікірлер: 13
Now this is what I really needed
@VictortheOrganicChemistryTutor
10 ай бұрын
Glad it helps 😁
This is just incredible, thank you alot!!!!
@VictortheOrganicChemistryTutor
23 күн бұрын
You're very welcome!
Brilliant ! Thank youuu
@VictortheOrganicChemistryTutor
5 ай бұрын
You're welcome!
why doesn't this have many more views? great vid. thanks!
@VictortheOrganicChemistryTutor
4 ай бұрын
Thanks to your comment, I’ll get a few more now 😅
thanks a lot
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
5 ай бұрын
That’s precisely the point. In order to assign the stereodescriptor, the lowest priority group must be looking away from the observer.
Can you tell me the meaning of non superimposable?
@VictortheOrganicChemistryTutor
5 ай бұрын
It’s when two objects are not the same no matter how much you rotate them in space.