I have a question for the last structure the one with 3 membered ring w/ a carbocation. I thought it was anti-Aromatic. My question is, do we take types of membered rings into consideration regarding its steric hindrance, angle strain? I remembered there was some cases that if it is 8 mb ring, or 3 mb ring have some exceptions right? Could you please help clarify, Sir? Thank you.
This was extremely helpful, everything finally clicked after the way you explained the concepts with so much detail. Thank you!
Many thanks, Sir. I am studying for an entrance exam to grad school now and it has helped me a lot!
This video help me a lot with chemistry exams in my university
BLESS x2 I love these videos where I can get so much practice
Glad they were helpful in your studies.
I thought when given the choice to be sp3 or sp2 it takes sp3 if it leaves it in a more stable conformation since nonaromatic is more stable than anti
very underrated
Excellent
Thank you, this is Amazing!
Why does the electron travel towards carbon if caron is not more electronegative?
Thx ❤
Excuse me sir.
The first question I thought the Hydrogen at the middle of the compound will make the compound not planar?
I have a question for the last structure the one with 3 membered ring w/ a carbocation. I thought it was anti-Aromatic. My question is, do we take types of membered rings into consideration regarding its steric hindrance, angle strain? I remembered there was some cases that if it is 8 mb ring, or 3 mb ring have some exceptions right? Could you please help clarify, Sir? Thank you.
Thank you ❤
Sir.., if I may ask, how we determine the total of phi electrons if the N atom no shows the lone pair?
In advance thank you very much for the video..
i didn't understand