<p>calbear - I did something different, but what you said actually makes sense because the HSO4 then is reprotonated by the alcohol’s H.</p>
<p>what are these journals of organic chemistry that he’s getting problems from? anyone ever tried finding them and memorizing mechanisms? haha</p>
<p>i doubt they show mechs though…it’s probably just the rxn…there’s like 1000s of journals out there probably too. you’d have to have photographic memory…which would be ****** awesome for ochem</p>
<p>lol yeah. so i’ve been working on problem set 11 all day and i finally feel like i know what i’m doing 
got everything right for 2 pages in a row yayy. sigh.</p>
<p>i’m sorta screwed, i have 2 finals tomorrow that i’m pulling an all-nighter for, and then i have to pull another all-nighter to study for 3b. and i slept 4 hours last night.</p>
<p>this is wut death must feel like, seriously.</p>
<p>seriously mech…what happened to that thread?</p>
<p>you know what I’m talking about :D</p>
<p>yes!</p>
<p>I FOUND IT…<a href=“http://talk.collegeconfidential.com/university-california-berkeley/926306-whos-studying-main-stacks-right-now.html[/url]”>http://talk.collegeconfidential.com/university-california-berkeley/926306-whos-studying-main-stacks-right-now.html</a></p>
<p>search computer history win…</p>
<p>page 3 midterm 2 last problem with the deuterium. how does it add on to the nonenolizable side? :(</p>
<p>Remove a proton from that carbon with the Meo-, you can move the charge all the way to the oxygen. And then just go back the other way and grab a D. Hope that makes sense haha.</p>
<p>I still can’t figure out why my Haworth projections for 1B were marked wrong…</p>