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Will the diketone formed in the final reaction tautomerize to the enol product since the pi bonds will be conjugated and then there are h-bonding interacts between the alcohol and carbonyl groups?
Mechanisms missing..! Kindly show the mechanisms in detail too.. That how a pyrrolidine got attached to ketone? 8:19 Is there any hydrogen bond formation? TIA
Wouldn't the nitrogen of the enamine be methylated preferrentially and just become a leaving group. I read that enamines work best with larger r groups
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MAY GOD BLESS YOU! You are truly a blessing to many of us here!! I am in uni and your videos helped me pass and understand Orgo1 and now I am here for Orgo2. wish all the best y'all!
THANK YOU SO MUCH, I HAVE AN EXAM THIS WEEK !
how did it went
Will the diketone formed in the final reaction tautomerize to the enol product since the pi bonds will be conjugated and then there are h-bonding interacts between the alcohol and carbonyl groups?
my quiz is in 20 minutes, good thing this is a 16 minute video
14 mins
Hello 👋 I wish you more more more prosperity. You have helped immensely. I hope I can meet you someday and personally thank you or give you a gift.
Thank you once again.
Sir. Please explain the equivalent of LDA reagents also...will helpful for us
Mechanisms missing..! Kindly show the mechanisms in detail too..
That how a pyrrolidine got attached to ketone? 8:19
Is there any hydrogen bond formation?
TIA
the steriochemistry is missing in LL THE FINAL PRODUCTS. We should have 2 products right One with wedge and dash?
Only if it began with stereochemistry.
Thank you so much because I have got in chemistry /1
Thanks 👍✌️
what happens with the kinetic product if there’s water (humidity) during the dry ice bath of the formation of LDA?
Wouldn't the nitrogen of the enamine be methylated preferrentially and just become a leaving group. I read that enamines work best with larger r groups
Exactly my doubt. Less reactive alkylating agents like in this case methyl bromide prefer reacting at nitrogen than at carbon.
I guess cuz the lone pair on the nitrogen is sterically hindered (big compound) and is in conjugation with the double bond.
So if its LDA, THF as my reactent i would trade out the alpha hydrogen for THF?
No, LDA simply abstracts the H+ from alpha position leaving a negative charge there.
what is the website/app u use in the drawing thing pls tell me
Tysm sir😊
Good
Interesting called one of the green alpha hydrogens red🤔 might be colorblind which is cool
Prol a slip of tongue
Hi could you please put the carbohydrate reaction video up for organic chemistry/ intro to biochemistry. it was deleted for some reason