THANK YOU for showing that intramolecular hydrogen bond! It was not explained in my notes or textbook and I could not understand how that enol was being formed. bless you!!
I normally watch these to study for engineering exams. Today I’m watching to see how the THC-A in my cannabis turns into the neutral THC in my edibles ;)
Why did the reaction have to pass through an Enol form? Would it be correct for the Carbanion formed on the alpha-Carbon to react directly with the first H+ lost from the --OH group to give us the desired ketone product instead of forming a double bond with the beta-carbon?
I didn't understand chemistry enough to get this. But I still want to know what goes on. What does the acid turn into or where does it go and how does that help your body accept it better. And does it really help it accept it better,? Or does it just make it into something that effects us in a way that we understand
@@whatthehell7975 but ,if the tautomerisation is occurring in a ring compound and the alpha hydrogen is present at the double bonded carbon atom , then tautomerisation won't occur
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20 essay and the deadline is tonight😭😭😭 thank you
THANK YOU for showing that intramolecular hydrogen bond! It was not explained in my notes or textbook and I could not understand how that enol was being formed. bless you!!
Cool, this is what happens when people heat up THC-acid to get THC molecule. Amazing stuff.
I normally watch these to study for engineering exams. Today I’m watching to see how the THC-A in my cannabis turns into the neutral THC in my edibles ;)
Best channel for class 11th students !!! Appreciate your hard work ☺️
For all
@@tanavposwalhe knows organic not like indian teacher who tells to cram everything
@@jyotisharma-le7fuif your teacher is bad doens't mean all Indians teach in the same way 🦆👍
@@adarshsuvedi2524 plz suggest me any good organic teacher in online platform in whole India who doesn't tell to cram organic.
Thank you for the mechanism! This helps me a lot.
You are amazing. Please continue the great work!
Why did the reaction have to pass through an Enol form? Would it be correct for the Carbanion formed on the alpha-Carbon to react directly with the first H+ lost from the --OH group to give us the desired ketone product instead of forming a double bond with the beta-carbon?
Heyy can you please make a video on Decarboxylation from sodium salts of carboxylic acid? Thanks!!
man is straight up carrying us
thank you so much for ur videos! you are amazing!
I didn't understand chemistry enough to get this. But I still want to know what goes on. What does the acid turn into or where does it go and how does that help your body accept it better. And does it really help it accept it better,? Or does it just make it into something that effects us in a way that we understand
acid turns into carbon dioxide (COOH --> CO2)
2:00 6 MCTS
Your voice is so good to hear
Zdravo pacenici i ja se patim
Thanks 😊
💖
Can tautomerization occur without water?
No
It only needs alpha hydrogen
@@whatthehell7975 but ,if the tautomerisation is occurring in a ring compound and the alpha hydrogen is present at the double bonded carbon atom , then tautomerisation won't occur
Thanks!
Can I say I love you?
thumbs down bc you literally drew one molecule at the beginning and then started the reaction with another.
Thanks
Stop using blue colors..., they are not clear visible