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carbene reaction conditions?
Only a tiny bit may have reacted I suppose; chloroform isn't appreciably soluble in a concentra ... |
22-5-2005 at 04:49
by: sparkgap |
carbene reaction conditions?
Yes, reacting chloroform with a strong, concentrated base will produce dichlorocarbene.  However, ... |
22-5-2005 at 03:21
by: sparkgap |
Permangates
Don't you mean "sodium permang[b]an[/b]ate", NaMnO<sub>4</sub>? If so, do ... |
21-5-2005 at 17:33
by: sparkgap |
What th..? (multi member bug?)
It also happens that after deleting what was supposedly one of your double posts, both posts are gon ... |
21-5-2005 at 06:51
by: sparkgap |
Stupid nomenclatura question
I was going to post a reply after seeing ORG's question, but apparently Mr. Wack and Kinetic be ... |
21-5-2005 at 01:55
by: sparkgap |
Sodium Aluminate
It's actually more of a complexation than a hydration in the particular reaction you mentioned, ... |
20-5-2005 at 23:01
by: sparkgap |
Sodium Aluminate
Something seems missing... isn't H<sub>2</sub> gas supposed to be evolved in this r ... |
20-5-2005 at 22:48
by: sparkgap |
Bismuth Crystals, etc.
"...you can use it as a laxative..."
Yeah, but lipid pneumonia isn't nice to have, ... |
20-5-2005 at 22:36
by: sparkgap |
Chromium isolation
From your description, the transient blue color does seem to be due to peroxychromate production. Th ... |
20-5-2005 at 03:28
by: sparkgap |
Indole from feces
"...has to be one of the nastiest extractions you could ever hope to do..."
You think? ... |
19-5-2005 at 08:38
by: sparkgap |
Question on making CH3NO2?
I see no reason for ammonium ion to readily cleave a nice and stable C-O bond.
That, and -OH is a ... |
18-5-2005 at 08:53
by: sparkgap |
Rotting Meat - a graphical treatise....
Where I'm from, [i]L. plantarum[/i] is commonly used for fermented sausages.
So what if chee ... |
18-5-2005 at 08:43
by: sparkgap |
Stove Elements?
Some engineers still tend to report quantities in English units (right, Magpie? 
), so deprecation ... |
18-5-2005 at 08:09
by: sparkgap |
How do I store I2?
Heating a bottle containing a substance that sublimes at whim is not exactly a good idea...
sp ... |
11-5-2005 at 07:46
by: sparkgap |
How do I store I2?
To answer cyclonite4's question, an iodine flask is utilized in the analytical technique of iod ... |
11-5-2005 at 07:29
by: sparkgap |
The recent unscheduled downtime
Man, all is good now. I thought someone was screwing around with our beloved board. What a relief.
... |
8-5-2005 at 06:07
by: sparkgap |
Theoretical Synthesis of 4-Piperidone/Piperidine
Were you referring to the "thiambutenes", Sandmeyer? I can attest to
that; when I tried ... |
7-5-2005 at 04:50
by: sparkgap |
Pseudonitrosites
Uh, chemoleo, sorry to burst your bubble, but any vinyl alcohol you might produce would spontaneousl ... |
6-5-2005 at 21:40
by: sparkgap |
retarding the growth to monocots
No, not the amine salt. I meant 2,4-D itself. Isn't it still available? I know it ain't ba ... |
6-5-2005 at 19:24
by: sparkgap |
Theoretical Synthesis of 3,4,5-Alkoxy-PEA
That was very funny, Sandmeyer. 
PainKilla:
"...if you don't mind me asking, do yo ... |
6-5-2005 at 18:23
by: sparkgap |
retarding the growth to monocots
If 2,4-D is still available there, that might work.
Otherwise, Google for "auxin analogs&quo ... |
6-5-2005 at 18:15
by: sparkgap |
My Chemistry book collection
Yep, but this guy is different (note the capitalization).
Don't we have "Experimental O ... |
5-5-2005 at 17:11
by: sparkgap |
home made damp rid
He lives in New Zealand (see his profile), so I doubt people would be selling de-icing salt there.
... |
5-5-2005 at 17:08
by: sparkgap |
Baking soda and gatorade... good sport drink?
With the carbonate buffer protecting the bloodstream and phosphate buffer protecting the kidneys, th ... |
5-5-2005 at 06:14
by: sparkgap |
Experimental Preparation of Chlorobutanol
Chloroform is very slightly polar, tom. The reason it's traditionally classed as a nonpolar sol ... |
4-5-2005 at 20:09
by: sparkgap |
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