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Alibi
Old 12-07-2007, 05:40 AM     Post subject: BOC #1 (permalink)  
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givememyleg
Old 12-07-2007, 10:21 AM #2 (permalink)  
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BOC YO

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givememyleg
Old 12-07-2007, 10:21 AM #3 (permalink)  
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no seriously WTF is that?!

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bode
Old 12-07-2007, 10:23 AM #4 (permalink)  
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Originally Posted by givememyleg
no seriously WTF is that?!
Quote:
eeevees are not monies yet...they are like baby monies.
 
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2_Thumbs_Up
Old 12-07-2007, 11:00 AM #5 (permalink)  
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some kind of ketone
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ProZachNation
Old 12-07-2007, 11:35 AM #6 (permalink)  
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a t-butyl on that carbonyl son
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I didn't think its Bold to bang some chick with my bro. but i guess so... thats +EV in my book.
 
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vqc
Old 12-07-2007, 11:52 AM #7 (permalink)  
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i <3 ochem!

how u enjoyin school alibi?
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Alibi
Old 12-07-2007, 02:48 PM #8 (permalink)  
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Originally Posted by ProZachNation
a t-Butyl On that Carbonyl son
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Alibi
Old 12-07-2007, 02:50 PM #9 (permalink)  
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vqc,

I love school so much it's becoming a problem for my gambling
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ProZachNation
Old 12-07-2007, 03:51 PM #10 (permalink)  
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organic chem final in 6 days, is cumulative from the past 2 semesters
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I didn't think its Bold to bang some chick with my bro. but i guess so... thats +EV in my book.
 
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Alibi
Old 12-07-2007, 07:36 PM #11 (permalink)  
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here are the answers to your exam

1) steric hindrance at the circled carbon determines the chemoselectivity
2) when you open an epoxide under lewis acid conditions, the regioselectivity is determined by the carbon that can best stabilize a positive charge, not the carbon that is the least sterically hindered
3)
a) TsCl, pyridine
b) DBU
giving you the alkene, followed by mCPBA
4) False, the pKa of acetic acid is too low.
TrapperAB: you know, I really should have named myself after the mandibles of a homeless person
 
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bigred
Old 12-07-2007, 07:52 PM #12 (permalink)  
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5) Profit
LOL OPERATIONS
 
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ProZachNation
Old 12-07-2007, 07:55 PM #13 (permalink)  
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Quote:
Originally Posted by Alibi
here are the answers to your exam

1) steric hindrance at the circled carbon determines the chemoselectivity
2) when you open an epoxide under lewis acid conditions, the regioselectivity is determined by the carbon that can best stabilize a positive charge, not the carbon that is the least sterically hindered
3)
a) TsCl, pyridine
b) DBU
giving you the alkene, followed by mCPBA
4) False, the pKa of acetic acid is too low.

if you can give me the next 71 answers you would be BOC
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iolzizlyi
Old 12-07-2007, 08:10 PM #14 (permalink)  
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organic chemistry is the reason i quit school. i'm back but now i'm a computer science major
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donkbee
Old 12-07-2007, 08:40 PM #15 (permalink)  
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I took two terms of organic chem and they are the only courses in my history of going to school where I went into the final exams failing

Needless to say, I dropped biochem as my major.



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ProZachNation
Old 12-07-2007, 08:52 PM #16 (permalink)  
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I AM THE SMARTEST MAN ALIVE because I'm probably gona get a solid C
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I didn't think its Bold to bang some chick with my bro. but i guess so... thats +EV in my book.
 
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vqc
Old 12-08-2007, 01:06 AM #17 (permalink)  
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Originally Posted by Alibi
vqc,

I love school so much it's becoming a problem for my gambling
same thing happened to me.
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Alibi
Old 12-08-2007, 02:38 AM #18 (permalink)  
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vqc, I think I'm going to an ACS conference sometime next year... if I do and you're going we should meet up
TrapperAB: you know, I really should have named myself after the mandibles of a homeless person
 
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jyms
Old 12-08-2007, 02:41 AM #19 (permalink)  
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I used to work with a shitload of N-butyls, normal propyls, Isobutyls and Methyl Ehtels. Do I get any points. Mostly alchohols, acetates and ketones. mostly dealt with drying times and pigments.
 
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Alibi
Old 12-08-2007, 02:47 AM #20 (permalink)  
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also, to address all of you who asked wtf that was, it's the group called tert-Butyloxycarbonyl, or BOC for short, used to protect alcohol groups
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Galapogos
Old 12-08-2007, 03:16 AM #21 (permalink)  
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Quote:
Originally Posted by Alibi
also, to address all of you who asked wtf that was, it's the group called tert-Butyloxycarbonyl, or BOC for short, used to protect alcohol groups
Umm yeah, no shit Sherlock


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ProZachNation
Old 12-08-2007, 04:17 AM #22 (permalink)  
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Quote:
Originally Posted by Alibi
vqc, I think I'm going to an ACS conference sometime next year... if I do and you're going we should meet up

Im taking the ACS test as a final... you wouldnt happen to have the study guide you could scan for me would ya?
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swiggidy
Old 12-08-2007, 04:23 AM #23 (permalink)  
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One of the greatest days of my life. End of 2nd quarter freshmen year, I find out I only need 2 quarters of english and 2 quarters of chem so I'm mother-fucking-done.

ship it
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(")_(")
 
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Alibi
Old 12-08-2007, 05:01 AM #24 (permalink)  
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Quote:
Originally Posted by ProZachNation
Quote:
Originally Posted by Alibi
vqc, I think I'm going to an ACS conference sometime next year... if I do and you're going we should meet up

Im taking the ACS test as a final... you wouldnt happen to have the study guide you could scan for me would ya? :D
bah I'm morally opposed to ACS standardized exams for ochem... they ask more about memorization than understanding of mechanisms and concepts. you're more likely to be penalized for not knowing the name of the reaction than the arrow-pushing.
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vqc
Old 12-08-2007, 06:50 AM #25 (permalink)  
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Quote:
Originally Posted by Alibi
vqc, I think I'm going to an ACS conference sometime next year... if I do and you're going we should meet up
being that im in Law School and all, I don't know if I will ever make it out to an ACS conference. =).

My intro to O-Chem class was all about theory, then Ochem 2 and 3 were pretty much all reaction memorization. Granted, its easier to memorize a reaction if you know how to push electrons. Also, the tests gave us a beginning product and an end product and we had to use all the reactions we memorized to piece together the reaction process.
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Miffed22001
Old 12-08-2007, 11:48 AM #26 (permalink)  
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Quote:
Originally Posted by Alibi
here are the answers to your exam

1) steric hindrance at the circled carbon determines the chemoselectivity
2) when you open an epoxide under lewis acid conditions, the regioselectivity is determined by the carbon that can best stabilize a positive charge, not the carbon that is the least sterically hindered
3)
a) TsCl, pyridine
b) DBU
giving you the alkene, followed by mCPBA
4) False, the pKa of acetic acid is too low.
now i know why my major is in english+politics!
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bigred
Old 12-08-2007, 03:05 PM #27 (permalink)  
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I'll take an econ optimization or a data modeling problem over this stuff anyday
LOL OPERATIONS
 
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