This video shows how the powerful electrophile, NO2+, can react with toluene to give the ortho nitro toluene molecule. It is a must-see video for fans of electrophilic aromatic substitution.
Thank you so much Sir. You are a life saver ❤. Because I swear these teachers that they have as teachers is useless. They just fly through the PowerPoint with no thorough explanation.
@pratimathapa65
3 жыл бұрын
Thank you,, sir It's a great to see your video,, u is more good than my teacher
@summerandfall1362
Жыл бұрын
This guy is too beast 🧠
@nika3666
4 жыл бұрын
Thank you so much!
@ВикторияШтейнера
4 жыл бұрын
thank you !! it’s really good explanation !
@atsedemariam-r5s
Ай бұрын
👏
@asasdfdd1238
7 ай бұрын
So does excess of sulphuric and nitric acid form tnt ?
@privatekitty6621
8 күн бұрын
yah
@abhay.maurya548
Жыл бұрын
Ya kyon se language hai
@joshuahisoler8589
3 жыл бұрын
does it form a oily layer?
@DrBob-fp6gp
3 жыл бұрын
I have not done this reaction. I presume the aqueous acidic layer separates from the organic layer and the product would be in the organic layer.
@darioferraris1121
3 жыл бұрын
how do you prevent over nitration?
@DrBob-fp6gp
3 жыл бұрын
If you monitor the course of the reaction with thin layer chromatography, you can see when the over nitration starts. Because the nitro group is deactivating, the second nitration is slower than the first one, so with careful monitoring you can get a high yield of the mono-nitro toluene.
@vatsaldhanuka3030
3 жыл бұрын
Does major product is Ortho and why not para
@DrBob-fp6gp
3 жыл бұрын
Both ortho and para are significant products of this reaction. You get about 2:1 ortho to para, mainly because there are twice as many ortho positions.
@vatsaldhanuka3030
3 жыл бұрын
@@DrBob-fp6gp NO BUT THIS REASON IS NOT FARE COZ IN OTHER REACTION PARA IS THE MAJOR PRODUCT
Пікірлер: 16