Easy R-S Configuration of Complex Molecules

An Easy Way To Determine R-S Configuration Of COMPLEX Chiral Compounds:
A Lot Of Examples
For a better understanding, it may help to watch our video "Easy R-S Configuration of Fischer Projections": • Easy R-S Configuration...
*Content Correct at ~8:30: oops... my bad... the alpha carbon below the chiral carbon is tertiary, while the carbons on the left and right are only secondary, which means the tertiary alpha carbon below the chiral carbon is priority 1 because it is higher order than the two secondary alpha carbons on the left and right; then the side with the carbonyl (C=O) on the beta carbon (right side) would be priority 2, and then left-side would be priority 3... minor but important oversight on my part
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[@ajaydugamer6433]

WOOOOO, what an eye opener vedio. Finally, my doubt got clear. Thank you :)

[@JohnJiap-dd1mr]

Thank you so much the explanation is very clear, Try to do one with the ciral carbon attached to one benzine ring 🥰

[@pokawinkoni1754]

Thank you for this video, helpful. It will be more helpful if you explain also the 2nd chiral carbon in the last example.

[@PraxisAcademic]

Thank You for the suggestion! I will definitely consider that when I redo this video in animated form. Thank You for watching.

[@455tyra]

The best video ever. As someone who has struggled with this for years thank you !!!!!!

[@PraxisAcademic]

Thank You!

[@jayantajithazarika2619]

Dear Madam , Thank you very much for your nice and fàntastic video . Please keep uploading many more such videos related to Chemistry . With lots of lots of love 💕💕💕💕💕 and regards , Jayantàda ,

[@PraxisAcademic]

Thank You so much for the encouragement!! I am working on finishing more Chem and Orgo videos and will upload as soon as possible.

[@chavakavitha1368]

Madam, in the last question i think the order of priority is wrong, the down carbon is attached to 2 carbons and one hydrogen so it should get priority 1 (which u gave as 3)

[@PraxisAcademic]

Nice catch! You are absolutely correct! Just making sure everyone is paying attention and watching the video all the way through… haha… JK. My mistake-the bottom carbon is tertiary, whereas the left and right carbons are secondary, so the bottom carbon should have been assigned priority 1, and then the side with the carbonyl priority 2, and the side with the quaternary carbon priority 3. Good thing it will still be counter-clockwise rotation and S-configuration… I at least got that right. 😁Thank You for pointing that out!

[@chavakavitha1368]

How can I contact you, Madam??

[@PraxisAcademic]

@@chavakavitha1368 I have the social media links and our website links on my KZbin channel with you can contact me.

[@denizuludogan9365]

THANK YOU SO MUCH!! Finally this semester I’ll be able to pass pharmaceutical chemistry hopefully😅

[@PraxisAcademic]

I am glad this helped. Pharm Chemistry is definitely a tough course! Thank You for watching.

[@manarchadli397]

Thank you so much I'm médical student 🩺 from Algeria 🇩🇿🇩🇿❤️ I

[@منیرهمحبی]

خیلی خوب بود

[@WondimaghineHaile]

❤ I love your teaching thank you

[@anonanon-rc7ib]

👍🏻

[@grindingTogether]

Tbf all love on you

[@homemobile8362]

Thank you madam❤

[@salwashoaib2718]

Amazing and clear explanation for this important MCAT topic!

[@PraxisAcademic]

Glad you think so!

[@wuincy1]

i love you

[@PraxisAcademic]

lol... thanks! And I hope this helped in orgo!