Atropisomerism: An overview

[@danysharma4790]

12 people are impatient people. This lecture is very clear one.🤘
Thank u so much sir.!

[@ChemWis]

Thanks for watching!

[@alderamin1402]

Why if there is steric hindrance between hydrogens in biphenyl, how could it freely rotate

[@randomgyan6584]

u r awesm sir

[@ChemWis]

Thank you brother!

[@sumalya2251]

Sir, plz explain more example from P, M nomenclature . 🙏🙏🙏🙏
U are great sir .

[@ChemWis]

Sure I will

[@ChemWis]

Video on P, M nomenclature has been uploaded: th-cam.com/video/UQLlDdQsuEg/w-d-xo.html

[@vinay_1990]

nicely explained, Sir!!

[@anjalivijayan8984]

Sir ,why atropisomerism disappear on heating?? pls reply

[@ChemWis]

Thanks for watching this video. Atropisomerism does not disappear on heating in all the cases. It does disappear only in the cases where the ortho-substitutents are of medium of size. Upon heating the average length of pivotal bond increases that allows free rotation about this bond and hence atropisomerism disappears.

[@anjalivijayan8984]

Thank you sir 😊

[@jayprakashprajapati8883]

very helpfull video sir, can you please share some reference book for this topic, thanks you

[@ChemWis]

Thank you for watching this video. It is Organic chemistry Volume 2 by I. L. Finar

[@tejassharma9726]

thank you very much

[@tanvikamat1369]

8:30 rs configuration

[@hrushikeshbarik5158]

Way more great than what UNACADEMY teaches us....🙏🏻🙏🏻🙏🏻 Great sir keep going

[@hrushikeshbarik5158]

I love ur way of teaching

[@ChemWis]

Thank you, I will

[@hrushikeshbarik5158]

@@ChemWis welcome sir u r great

[@ushasingh9944]

Good sir

[@ChemWis]

Thanks

[@subrahmanyamponnada7159]

Lucid explanation

[@ChemWis]

Thank you!

[@jineshmenaria8748]

Nice

[@ChemWis]

Thanks

[@meghanamagi2475]

Nice sir

[@ChemWis]

Thank you!