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Organic reactions database
This is an excellent collection of bare-bones information on organic reactions.
http://www.chempe ... |
28-4-2003 at 19:23
by: madscientist |
Whoopsie
Yes, other people's posts are safe. |
28-4-2003 at 14:38
by: madscientist |
nitrobenzoyl peroxide
Don't nitrate benzoyl peroxide. Nitrate toluene, oxidize to the nitrobenzoic acid, then prepare ... |
27-4-2003 at 16:44
by: madscientist |
Glad to hear you're okay so far
Here's a good page with information on pulmonary edema. Check it out. http://www.nlm.nih.gov/me ... |
27-4-2003 at 16:38
by: madscientist |
nitrobenzoyl peroxide
Nitrobenzoyl peroxide will probably be extremely sensitive! The nitro groups on the aromatic rings w ... |
27-4-2003 at 15:41
by: madscientist |
SECURE YOUR GAS MASK!!
As for pulmonary edema: you know you have it if you have trouble breathing when lying down, but don& ... |
27-4-2003 at 15:34
by: madscientist |
Willgerodt Reaction
Quite a useful synthetic reaction! Some of us probably immediately thought "phenylacetic acid!& ... |
19-4-2003 at 08:56
by: madscientist |
Willgerodt Reaction
<b>This post is an excerpt from an advanced organic chemistry textbook.</b>
ArCOCH< ... |
19-4-2003 at 08:52
by: madscientist |
Reduction of carbonyl groups
I'm guessing he was wondering how to prepare an oxazoline from propenylbenzene.
How about us ... |
18-4-2003 at 19:50
by: madscientist |
Reduction of carbonyl groups
The molecules you diagrammed are the ones I had in mind.
I actually was shooting for a different ... |
16-4-2003 at 00:47
by: madscientist |
Nitric acid
The purpose of the electric arc isn't really to electrolyze air - it's to create temperatu ... |
15-4-2003 at 23:08
by: madscientist |
Reduction of carbonyl groups
I'm not sure what those acronyms stand for. 
I'm wanting to dehydrate 1-phenylpropan- ... |
15-4-2003 at 23:05
by: madscientist |
H2SO4
Yes, that will increase the concentration. Typical H<sub>2</sub>SO<sub>4</sub&g ... |
15-4-2003 at 22:24
by: madscientist |
Had an acciedent.......
If you want a real mess, try dissolving nickel alloys in an aqueous solution of ~25% Caro's aci ... |
15-4-2003 at 22:22
by: madscientist |
Light sensitive compount storage
PE = polyethylene, which is susceptible to oxidation - nitric acid is a powerful oxidizing agent. Th ... |
15-4-2003 at 22:19
by: madscientist |
Reduction of carbonyl groups
The substrate for reduction would be 1-phenylpropan-1-one. |
15-4-2003 at 22:15
by: madscientist |
Elemental bromine isolation
Oops, I just realized that I forgot to post about the results of my second plan (the one involving n ... |
15-4-2003 at 12:16
by: madscientist |
Reduction of carbonyl groups
Will reduction of a carbonyl group with Al/Hg amalgam yield an alcohol, or will the reduction go all ... |
15-4-2003 at 09:36
by: madscientist |
Kitchen chemistry
[quote]Madscientist, if it´s your kitchen and you use it as lab...[/quote]
Huh? I hadn't po ... |
13-4-2003 at 20:35
by: madscientist |
Sodium Azide
I think sodium azide simply isn't a very powerful explosive.
Lead is definitely worse for th ... |
13-4-2003 at 19:25
by: madscientist |
Sodium carbonate?
Merck on Na<sub>2</sub>O: "Melts at a dull red heat and begins to dec >400degree ... |
12-4-2003 at 18:29
by: madscientist |
Readily Available Chemicals Website
Trichloroethene is sold as "Carbo Sol," a solvent. Glycolic acid is sold as "Sucanat, ... |
12-4-2003 at 16:09
by: madscientist |
Sodium carbonate?
Cappy, H<sub>2</sub> isn't generated by heating sodium bicarbonate, it was a typo. ... |
12-4-2003 at 14:51
by: madscientist |
Separatory Funnel
What's slowing down the separation? I've never had troubles with separation taking forever ... |
12-4-2003 at 04:34
by: madscientist |
Sodium carbonate?
The reaction requires fairly high temperatures, isn't exactly furiously rapid, and there is no ... |
11-4-2003 at 20:08
by: madscientist |
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