Feel I may get lost in the sea of compliments, but Sal..once again you have succeeded in helping a very confused, mature, Open University Student to become a LOT less confumbled! Keeping doing what you do best, stimulating neurons without scaring them lol!
If the electrophile is a halogen, the bond can be polarised by using a Lewis acid catalyst. If the electrphilic substitution is a sulphonation, then no Lewis acid is necessary, and the proton reacts with the sulphonate anion, forming the sulphonic acid.
Could you add/include an orbital visualization of these processes in organic chemistry? Maybe in all (following) chemistry videos? Thank you. Keep on going.
These video are amazing!!! Thank u so much from italy :)
folkytos 1 week ago
like someone already said, UR THE MAN :]
baby00040007 1 month ago
I have watched all your videos. THEY ARE AWEEEEEEEEEEEEESOME. thank you.
Do you have "Nitration of benzene mechanism"?
MrMedris 1 month ago
Why did the base go for the hydrogen instead of the carbocation?
kourosh89 2 months ago
"It wants electrons really, really, really, really, REALLY bad!!" haha you are the man , thanks so much for this.
manutdfan4321 3 months ago 6
Feel I may get lost in the sea of compliments, but Sal..once again you have succeeded in helping a very confused, mature, Open University Student to become a LOT less confumbled! Keeping doing what you do best, stimulating neurons without scaring them lol!
lynz60 3 months ago
Thank you sooo much. You are going to help me pass my finals!
rosefiona22 1 year ago 11
Oh my goodness!! Just what I need!!!
thenicolochy 1 year ago
Great videos...thank you! What program/hardware are you using to draw/record?
drjsteinberg 1 year ago
If the electrophile is a halogen, the bond can be polarised by using a Lewis acid catalyst. If the electrphilic substitution is a sulphonation, then no Lewis acid is necessary, and the proton reacts with the sulphonate anion, forming the sulphonic acid.
philsaspiezone 1 year ago
Could you add/include an orbital visualization of these processes in organic chemistry? Maybe in all (following) chemistry videos? Thank you. Keep on going.
norwayte 1 year ago