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All Comments (11)
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These video are amazing!!! Thank u so much from italy :)
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like someone already said, UR THE MAN :]
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I have watched all your videos. THEY ARE AWEEEEEEEEEEEEESOME. thank you.
Do you have "Nitration of benzene mechanism"?
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Why did the base go for the hydrogen instead of the carbocation?
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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!
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Oh my goodness!! Just what I need!!!
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Great videos...thank you! What program/hardware are you using to draw/record?
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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.
Thank you sooo much. You are going to help me pass my finals!
rosefiona22 1 year ago 11
"It wants electrons really, really, really, really, REALLY bad!!" haha you are the man , thanks so much for this.
manutdfan4321 3 months ago 6