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Decarboxylation-what is soda lime for?
"Calcium would also have a natural affinity for CO2."
Yes, and so does NaOH, which is the ... |
23-1-2004 at 10:35
by: Theoretic |
Decarboxylation-what is soda lime for?
Now, I think this belongs in the Beginnings section. The soda lime is actually the thing that decarb ... |
23-1-2004 at 07:23
by: Theoretic |
HexaChloroEthane Synthesis?
Maybe addition of hydrogen chloride to cyanogen (addition across the triple bind) will help...  |
22-1-2004 at 07:17
by: Theoretic |
h202 concentration?
Another way to concentrate H2O2 is to add an anhydrous salt that forms hydrates readily. For example ... |
21-1-2004 at 07:26
by: Theoretic |
Understanding detonation alittle better
Hmmm... ...so why, in almost every article about high explosive compounds I meet there's inform ... |
21-1-2004 at 02:06
by: Theoretic |
New sections
"Maybe we should have a poll about this."
by chemoleo.
I think so too, so let's see ... |
16-1-2004 at 11:01
by: Theoretic |
New sections
“PS2 So now there are two suggestions for New Forum Fields:
1. A section for all the clo ... |
16-1-2004 at 05:55
by: Theoretic |
Bogus posters
The option I propose is: just ignore it! Continue the discussion like it's not there. This was ... |
16-1-2004 at 05:37
by: Theoretic |
Acetic acid/ sodium hydroxide
Maybe it will form acetone and copper carbonate (like the calcium salt) and then the carbonate will ... |
16-1-2004 at 02:56
by: Theoretic |
metallic acetelydes!!!
Just SEARCH. Google usually works.
*fume* |
15-1-2004 at 10:50
by: Theoretic |
Bogus posters
I think so too. |
15-1-2004 at 08:25
by: Theoretic |
SnCl2 or SnCl4
Sn IS more reactive than H2, its oxidation potential is -0.136 V, which is why it can dissolve in ac ... |
14-1-2004 at 10:42
by: Theoretic |
Chlorine
Decomposition of nitrogen trichloride... |
14-1-2004 at 05:30
by: Theoretic |
OMG, What the f--- Please I need help!!!
"BRIGHT orange"
I have once hydrolysed some Fe(lll) salt in very hot water, in hope of ma ... |
13-1-2004 at 10:46
by: Theoretic |
OMG, What the f--- Please I need help!!!
The oil on top...
Well, the only thing I can think of is chromyl chloride, the formula is CrO2Cl2, ... |
13-1-2004 at 07:28
by: Theoretic |
Sodium!
On the topic of separation of sodium from carbon that fell off the electrode... ...sodium forms sodi ... |
13-1-2004 at 05:38
by: Theoretic |
Ancient Potash Making.
Mr. Wizard:
See my post at "User names and boredom..." in Whimsy. |
12-1-2004 at 11:20
by: Theoretic |
Bogus posters
I think Acid Test resurfaced again.. ...this time it's Sean Ambrose. I think he changed his IP ... |
12-1-2004 at 08:10
by: Theoretic |
copper fulminate
"I read somewhere that methylene group in neighborhood with a carbonyl group reacts with nitrou ... |
12-1-2004 at 07:44
by: Theoretic |
copper fulminate
What I mean is that nitrous acid bonds to the intermediates in the process by eliminating an oxygen ... |
10-1-2004 at 03:06
by: Theoretic |
Bogus posters
I've deleted all of my irrelevant posts myself and stayed a regular... ...just. |
9-1-2004 at 11:30
by: Theoretic |
Acid Test
"Why do you need my pager number?"
No one, no more...
Acid Test could just use a differe ... |
9-1-2004 at 11:05
by: Theoretic |
Chlorination of Alkylamines to Nitrogen Mustards
"Actually I think that SO2+2HCl=H2O2+SCl"
No. That, and it's not balanced. |
9-1-2004 at 10:43
by: Theoretic |
copper fulminate
It looks like COPAE's reaction only differs in that formic acid is oxidized with more nitric ac ... |
8-1-2004 at 08:02
by: Theoretic |
Ethylene explorations
I take that as a "no".
BTW, this is my 250-th post. Now I'm a regular!  
& ... |
7-1-2004 at 10:08
by: Theoretic |
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