In the second case with Carbon and Na the partially negative Carbon closest to the Na should attract electrons from the other carbons and not share negative charges. Also when you have a carbonyl group you have partial charges, the oxygen has a parital negative charge and the carbon a paritla positively charge. If you take the two electrons of the pi bond and you make the oxygen fully negatively charge, the carbon which is now positively charge too helps the stabilization of thevnegwtive charge but it doesnt become paritally negative as you show here. Very bad represenration of the matter.
![Lp. Сердце Вселенной #60 РОЖДЕНИЕ ЛОЛОЛОШКИ [Финал] • Майнкрафт](http://i.ytimg.com/vi/YoR0pAV9FVQ/mqdefault.jpg)
Make videos on hyperconjugation and resonance too
Very nicely explained. Thankyou.
Make more organic chemistry video
thank you. this one is so helpful. easy to understand.
Wow! Thank you so much🙏
Thank you 😊 😊 💕 💕💕💕
THANK YOU! very simple explained :))
Thanks!!
Masterclass
Who is the teacher?
Doesn't O has more en than c?
yes
O has more EN than C, but O- is already negatively charged so it doesn't want any more electrons, and pushes them away.
He explained why he did that. It's O-
In the second case with Carbon and Na the partially negative Carbon closest to the Na should attract electrons from the other carbons and not share negative charges. Also when you have a carbonyl group you have partial charges, the oxygen has a parital negative charge and the carbon a paritla positively charge. If you take the two electrons of the pi bond and you make the oxygen fully negatively charge, the carbon which is now positively charge too helps the stabilization of thevnegwtive charge but it doesnt become paritally negative as you show here. Very bad represenration of the matter.