Hey your videos saved me for my second exam (rxns at the alpha carbon). Do you have any other videos up that would help with amines? other than this one
Ivan Duy fantastic question! hydroxide absolutely causes hydrolysis of amides. and i can understand your confusion, because in my mechanism i show ONLY the amide and hydroxide at the start of my mechanism. IF only amide and hydroxide were present, hydrolysis would occur. however, because BOTH bromine (Br2) and hydroxide are present at the start of this reaction, equilibrium favors the mechanism shown in the video.
Finally got it! thank you.. only person who knows how to explain it
Your explanation is very good
Thanks mam, love from India 😊❤️
Good efforts god bless you madam
Thank you
Appreciate your great effort
Nice explanation
Hey your videos saved me for my second exam (rxns at the alpha carbon). Do you have any other videos up that would help with amines? other than this one
WHAT PRODUCT WILL BE OBTAINED WHEN WE USE AMIDE HAVING -OH GROUP IN PARA POSITION IN HAFMANN REARRANGMENT
why does alkyl rearrangement happens?
Tnx mam
At decarboxylation stage at the end i think the lone pair of nitrogen supposed to attack the H bonded to Oxygen , is that possible ?
Why hydroxide ion doesn't hydrolysis amides ?
Ivan Duy fantastic question! hydroxide absolutely causes hydrolysis of amides. and i can understand your confusion, because in my mechanism i show ONLY the amide and hydroxide at the start of my mechanism.
IF only amide and hydroxide were present, hydrolysis would occur.
however, because BOTH bromine (Br2) and hydroxide are present at the start of this reaction, equilibrium favors the mechanism shown in the video.
Janci Despain Ok , thank you very much.
This mechm is a monster
i love u..
"Ugly orientation" 🤣🤣
your so beautiful 😍