No, Shems, thank YOU for watching! Make sure to check out my actual website joechem.io for all my videos + guided worksheets & solutions (still working on finishing the worksheets for the tail end of OChem II). And, if you'd subscribe to my RUclips channel, I'd be forever grateful.
Hey Caio! I salute right back atcha, and as far as I know, thank you watching/being the first jOeCHEMist from Québec 🤓! Without seeing a specific problem, it's hard for me to definitively say, but it sounds like your rearrangement situation might lend itself to forming an enamine, which could remain as it is or (if in acidic conditions + H2O) could unravel and become a carbonyl. I hope that answers your question, and thank you again so much for watching!
im not a industrial chemist but by looking at it i can logically come at a conclusion about what could be its use. we can find hydrocarbons from oil , coal, and if we find some hydrocarbons which can be modified via this reaction to provide much more useful hydrocarbons then it is very much efficient since all we need to do is just heat and there will be high yield for the required compound. so its important in some cases.
Omg you're the best. TYSM
You're the best! Thanks for watching 🤓
OMG THANK YOU!!!
I think the last reaction is called an Oxy-Cope Rearrangement, but I might be wrong.
thank you :)
No, Shems, thank YOU for watching! Make sure to check out my actual website joechem.io for all my videos + guided worksheets & solutions (still working on finishing the worksheets for the tail end of OChem II). And, if you'd subscribe to my RUclips channel, I'd be forever grateful.
Hey Joe, all my salute from Québec to you, I have a question. If we had a secondary amine instead of the alcohol, would we still have tautomérisation?
Hey Caio! I salute right back atcha, and as far as I know, thank you watching/being the first jOeCHEMist from Québec 🤓!
Without seeing a specific problem, it's hard for me to definitively say, but it sounds like your rearrangement situation might lend itself to forming an enamine, which could remain as it is or (if in acidic conditions + H2O) could unravel and become a carbonyl.
I hope that answers your question, and thank you again so much for watching!
Could you do more complicated ones that requires correct stereochemistry?
ty
yw!
where can I find the worksheets?
@lore I've just updated the video description with the worksheet links -- let me know if you have any issues accessing it or the solutions!
thank you very much!!!! 😊
what even is the purpose of this reaction
im not a industrial chemist but by looking at it i can logically come at a conclusion about what could be its use.
we can find hydrocarbons from oil , coal, and if we find some hydrocarbons which can be modified via this reaction to provide much more useful hydrocarbons then it is very much efficient since all we need to do is just heat and there will be high yield for the required compound. so its important in some cases.