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abb0t
 one year ago
Best ResponseYou've already chosen the best response.1\(\sf \color{red}{[NOTE}\): \(\sf \color{}{this ~one ~is ~tough!]}\) Starting with \(benzene\) and using alkanes/ carbonyls with \(3\) carbons or less, propose a mechanism that will yield this product: dw:1382816587946:dw

aaronq
 one year ago
Best ResponseYou've already chosen the best response.2dw:1382837096210:dw dw:1382837326902:dw

aaronq
 one year ago
Best ResponseYou've already chosen the best response.2wait i would protect the carbonyls first with dw:1382837725077:dw

abb0t
 one year ago
Best ResponseYou've already chosen the best response.1Wow. Nicely done @aaronq you must be getting an A in orgo right now. This one gave me a headache when I first got it in class.

aaronq
 one year ago
Best ResponseYou've already chosen the best response.2thanks dude. I had orgo last semester (in the summer) and pulled off a decent mark. right now i have OC of biological molecules (carbohydrates, peptides) and theres so much going on, so this stuff seems a lot simpler now. Thanks for posting this up, they're good refresher exercises.

abb0t
 one year ago
Best ResponseYou've already chosen the best response.1I never got into that, we did it briefly in OChem. but I did do biosynthesis of macromolecyles, but that was my last biochem course.
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