I don't get rid of the TPPO because I usually run Horner-Wadsworth-Emmons, aqueous workup

Very helpful and simple explanation thanks

It would be helpful to include detailed procedures for separation and purification, which are crucial steps in the synthesis process.This would greatly enhance the your videos educational value.

Thanks Sir

Poorly explained couldn't understand anything

great video where you have been all this time . thank god that i found this channel

Thanks for the clear and informative video! Great explanation of the Mitsunobu reaction! The detailed breakdown of the mechanism and experimental setup is really helpful for understanding this complex process.

Great walkthrough of the hydrogenation reaction setup! The detailed steps on reducing nitrobenzene to aniline, along with the emphasis on safety, make this video really informative. It's a great resource for anyone learning organic chemistry!

Thanks for the content! plz more of it :D

Which palladium catalyst you used?

cool

Give that pdf....na sir... In pdf manner

You did not have any problems with triphenylphosphine oxide and doing flash chromatography. I usually had to remove that first...by recrystallization of the oxide. There was no ZnCl/methanol method yet.

I love Sodium sulfide or Sodium bisulfite in aq. MeOH condition for -NO2 to -NH2 conversation

Really nice 😊

it would be nice if you make a video about meinwald rearrangement -a member of turkish chemistry olympiads

Mention name of product please

Greetings from the Turkish Chemistry Olympiads🫡

what is the name of the song used as the background music?

Hi what do you think is the pka of dimethylphenacylsulfonium tetrafluoroborate and do you think if there is any acidic protons that can dissociate?

Really cool chanel! I went and looked at Narasaka-Prasad, just as a refresher. Subscribed!

Acid chloride!!! column seperation????

Thanks for the detaild explanations ;)

Thanks for education

I want to synthesize the ganiothalamine and in my protocol, I have a step where I need to make the mitsunobou reaction. I need more information please.

Hello! Can you tell me how much réactifs you used? I mean the quantity of each réactif.

Beautiful, I admire your presence, the mechanism helps a lot

Cool reaction, nice music too 👌

Wow you are really good at typing and creating easy to follow diagrams. What program/platform do you use to make the process quicker?

Does this actually work well with tertiary alcohols? I learned it is not common to use it on tertiaries because it doesnt work that well.

nicely explained in short time.

and how do we remove an Alloc protective group for example ?

Best explanation of mechanism using chemdraw ❤

Will u put video on mc murray and metathesis reaction mechanism sir

Can you explain how to convert thionoester using H2S & pinner salt

Kia bakwas samjhaya he

Music made this 10x better

Hi Lluís! This is Robert. Great video! Nice addition to your book.😍

why would you choose to add LiOH as the powder separately and not as aqueous solution?

Cool!

Helpfull vid, thanks 🫶🏻

thank you so much!!!!!!! this was so helpful

PERFECT

for the carbonyl with alkene, why does r-nh2 attack alkene and not carboynl

Easy to understand tnks

Thank you for the video

je pense que ce type de video ou l'on cherche a comprendre sans que vous fasiez la moindre explications n'aide pas du tout

Obtaining primary amines from nitriles requires ammonia presence (or other organic base), not acetic acid; Additionally raney nickel requires really high pressure, over 30atm, not just baloon.. Did You received anything beside starting material here?

Fire Musics!!!🤯

Thank you so much❤can i ask what is the function of each chemical group in this molecule?