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thank you so much, this made me understand the compounds better, also can you please put the handout in the discription?

You’re a life saver

Great work sir

Lanet olsun bu şeye

*Promosm*

Thank you very much for the only detailled step-by-step implementation in Python I could find! Really great, could follow along well and understood the concept. Yet, I seem to have an erorr in my code. The dictionary throws KeyErrors (even after the fix at 30:45) and when I fix that by using order_of_ids.get(), I still get different results than skimage. I will watch your video again, it must be my misstake. But it would be really nice if you share the code used so I can compare. The code in the repo is different (I guess from the soon-to-come part 2?) Anyways, thanks a lot :)

My lecturer gave me a tough time in class so backing up with this tutorial vid helped me a lot to name and be able to draw the structures Thanks so much

Azocine is the right answer at ,7:35

thank u

thank you man, beutiful series. thank god i was able to come across your videos

Thank you sir soooooooooo much for these educated videos Please sir do you have a Facebook account l have a questions regarding the organic chemistry. If you have please could you refer it to the comment

This was so incredible! Thank you so much for your help!

How about the rules for numbering Tricyclic structures?!? Including tricyclic structures that contain a combination of both benzene and cyclo fused rings?

Bu ne ya abi niye dünya ya bunu dayatiyirsunuz

Good

Good

Hello about the nomenclature of the heterocycle in minute 7:35 isn't the right answer azocine ? also thank you very much for this amazing video

Very good 👍

Thank you very much but please the screen is blur

Thank you very much but please the screen is blur

please the screen is blur

Nice class

CORRECTION !!!!! On page 18 at the top of the notes and at 0:52 it should say: Pyridines as Nucleophiles: Electrophilic Aromatic Substitution • 6-Membered heterocycles are electron poor so are not good NUCLEOPHILES. • The nucleophilic nitrogen lone pair reacts first, creating a pyridinium salt whose positive charge makes the system even less NUCLEOPHILIC. Then the electrophilic aromatic substitution occurs and finally, salt breaking delivers the product.

Haha is this babybell?