Sciencemadness Discussion Board
Not logged in [Login ]
Go To Bottom

Search
ethyl acetate
Sorry to bump an old topic, but I thought I'd share my revised synthesis of this sweet smelling solv ...
26-5-2011 at 23:32
by: cheeseandbaloney
oxidizing limonene to carvone/carveol
[rquote=206051&tid=15938&author=Nicodem]
Which reaction are talking about? Do you mean the ...
6-4-2011 at 17:18
by: cheeseandbaloney
oxidizing limonene to carvone/carveol
[rquote=205953&tid=15938&author=blogfast25]cheeseandbaloney:

The choice of trihaloacetic ...
5-4-2011 at 19:26
by: cheeseandbaloney
oxidizing limonene to carvone/carveol
[rquote=205801&tid=15938&author=blogfast25]Much of organic chemistry is a bit of a distant h ...
4-4-2011 at 20:45
by: cheeseandbaloney
help with mechanisms
hmmmm so first hope your holidays went fantastically grand, second! Sandmeyer, goofed around with it ...
25-12-2010 at 23:13
by: cheeseandbaloney
help with mechanisms
yo sandmeyer! does it involve any tautomerization out of curiosity?
23-12-2010 at 21:57
by: cheeseandbaloney
Make Potassium (from versuchschemie.de)
I'm more of a browser than a poster, but I just wanted to say that I fucking love you sciencemadness ...
18-12-2010 at 13:38
by: cheeseandbaloney
help with mechanisms
yo Arrhenius! Why does the iodide specifically attack the methyl group and not the carbonyl carbon? ...
14-10-2010 at 00:43
by: cheeseandbaloney
help with mechanisms
Hey, another quick mechanistic question! Was flipping through some of the chapters in one of my orgo ...
2-10-2010 at 21:43
by: cheeseandbaloney
Anyone got ideas? MCPA to 2,5-dihydroxytoluene...
[rquote=186921&tid=14351&author=Sandmeyer][rquote=186007&tid=14351&author=Nicodem]
...
6-9-2010 at 02:01
by: cheeseandbaloney
Strange purple compound when oxidizing p-aminophenol
could it be a compound like methyl yellow perhaps?
4-9-2010 at 00:25
by: cheeseandbaloney
Piperic acid oxidation to Piperonal
[rquote=186187&tid=13857&author=Hexagon][rquote=186176&tid=13857&author=cheeseandbal ...
26-8-2010 at 12:09
by: cheeseandbaloney
Piperic acid oxidation to Piperonal
I would think the reason the oxidation of piperic acid usually fails because the strong oxidizers co ...
25-8-2010 at 20:39
by: cheeseandbaloney
help with mechanisms
great discussion! love this shit.

[b]un0me2[/b]

Is there a '3d' mode for Symyx Draw? I do like ...
18-8-2010 at 21:54
by: cheeseandbaloney
p-hydroxybenzaldehyde?
I would think that since -H has a higher 'migratory aptitude' (faster than a -Ph group) Baeyer-Villi ...
16-8-2010 at 18:53
by: cheeseandbaloney
help with mechanisms
[rquote=185220&tid=14305&author=kmno4]
"Very strong understanding of mechanism" is not the ...
14-8-2010 at 13:06
by: cheeseandbaloney
help with mechanisms
Thanks Arrhenius, and everybody! I feel I basically mastered everything in orgo 1 in my opinion, wit ...
13-8-2010 at 20:28
by: cheeseandbaloney
help with mechanisms
[rquote=185095&tid=14305&author=Arrhenius]If you enjoy pondering or working through organic ...
13-8-2010 at 01:16
by: cheeseandbaloney
help with mechanisms
oh wow, I was just overlooking the chloride shifting over a carbon! derp. I knew the ring strain was ...
12-8-2010 at 22:23
by: cheeseandbaloney
help with mechanisms
I wasn't sure where to put this, so I thought I'd ask here first. For any of the organic chemists ou ...
12-8-2010 at 15:40
by: cheeseandbaloney
chloral hydrate synthesis
Hey I'm young (my birth year is '84), but people like this are what give amateur chemists a bad name ...
4-7-2008 at 21:28
by: cheeseandbaloney

  Go To Top