You remind me of Joey from Friends, just smarter. Thanks for your work bro.
@Tina-xw8mbАй бұрын
This! 👆
@mitcho54523 күн бұрын
I WAS JUST THINKING THIS AHH😂
@jeremyharrison92654 жыл бұрын
you are awesome, just came across your channel and these are one of the best explanations I have seen. Thanks!!
@jOeCHEM4 жыл бұрын
Jeremy, thanks a ton, man! I've since made a second video on this topic kzbin.info/www/bejne/hpqpoYdoj92qntk (I go a bit more in depth because you can get a different double bond if you have a ylide thats attached next door to an aromatic system). Make sure to check out joechem.io/videos/38 where I have a worksheet + solutions linked (literally for free). And if you subscribe that would be H U G E L Y appreciated :)
@kenhagiya565 Жыл бұрын
JoeChem saving my ass once again. Thank you for the videos!
@mohammadsaifullahkhan533 жыл бұрын
This channel is awesome!!!
@tharushimunasinghe17164 ай бұрын
Thank you soomuch ❤
@meryammaryam43482 жыл бұрын
Thank you my friend🤗
@Sophia-rl5ph2 жыл бұрын
Thank you so much, I really appreciate you!
@irem99556 ай бұрын
would be better if you also solve questions which wittig is involved as a step. more complex questions pls
@jOeCHEM6 ай бұрын
Check out kzbin.info/www/bejne/hpqpoYdoj92qntk
@stormydoctor90096 ай бұрын
hi you know for the lda how it deprotonates less sterically hindered alpha hydrogens why did it deprotonate the sterically hindered alpha H's
@stormydoctor90096 ай бұрын
why not just use NaOme if you deprotonated the least sterically hindered H's
@jOeCHEM6 ай бұрын
It does because LDA is VERY large, so it is hard to reach more "crowded" alpha H's. So it is lazy and opts for alpha H's that are less sterically hindered, aka more accessible. Something like NaOMe is MUCH smaller, so it can access more "crowded" alpha H's.