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OpenStudy (nincompoop):
OpenStudy (nincompoop):
hero (hero):
Hmm, this group could probably use an expert in Chemistry.
OpenStudy (nincompoop):
@mathblonde
OpenStudy (nincompoop):
@zbay
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OpenStudy (nincompoop):
@satellite
OpenStudy (anonymous):
is satellite a chem expert too lol
OpenStudy (nincompoop):
@Callisto @radar @85295james @robtobey
OpenStudy (anonymous):
sorry i dont know =(
OpenStudy (nincompoop):
@Carl_Pham
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OpenStudy (bakonloverk):
im so sorry but idk
OpenStudy (nincompoop):
thermal isomerization
OpenStudy (abb0t):
Which one am I looking at @nincompoop haha
OpenStudy (nincompoop):
any
OpenStudy (abb0t):
The first one looks like a reaction within itself. Kind of like decarboxylation of beta-ketoacids. The second one I don't know the detailed mechanism, but I do know that it forms aromatic rings with alkynes, in room temp.
And the last one, I would use resonance to argue the 1,3-methyl shift :)
RESONANCE is everything in o-chem II, haha.
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OpenStudy (nincompoop):
LOL
OpenStudy (abb0t):
Do you have the answers? I am curious abt the second one.
The first one i probably could of answered 2 years ago. haha. I'd have to dig in my notes tho. But it seems it has something to do with resonance and temp haha.
OpenStudy (abb0t):
The second one looks familiar. Lol.
OpenStudy (abb0t):
I feel like a failure now :( Lol
OpenStudy (nincompoop):
lots of chemical biology
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