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Chloroacetic acid...
Well the reaction of alkyl halides with alkali nitrites produces nitro AND nitrito compounds - accor ... |
10-11-2003 at 09:03
by: Theoretic |
Nitromethane extraction
Nitromethane is in fact very hard to ignite with a match, and if it does burn, it does so with a laz ... |
10-11-2003 at 08:32
by: Theoretic |
Ethylene explorations
Quote:
"The hypochloric acid will actually go to chlorine gas, hydrochloric acid, and water in ... |
10-11-2003 at 08:03
by: Theoretic |
Chloropicrin and its Odor
I think the crusty stuff was a trichloronitronate of the metal of the lid (or a mixture of trichloro ... |
10-11-2003 at 07:45
by: Theoretic |
Ethylene explorations
1)Saturated hydrocarbons (preferably from petrol) => cracking it as far as it goes over a broken ... |
31-10-2003 at 08:40
by: Theoretic |
Eliminating NO2 from HNO3
"Something seems fishy with the H2O2 idea. After the H2O2 has given up an O to become H2O, why ... |
31-10-2003 at 06:49
by: Theoretic |
Extracting Sodium from Sodium Chlorate
"That Reaction is incorrect
That last reaction does not happen."
What, 2K+2KOH=>2K2 ... |
31-10-2003 at 06:43
by: Theoretic |
PVN
I think you can use straight polymer to make PVN. I suggest:
1)Dissolve PVC in a polar organic solv ... |
31-10-2003 at 06:26
by: Theoretic |
Concentrated nitric acid storage tank(98% HNO3)
Aluminium carbonate doesn't exist, actually. |
24-10-2003 at 10:51
by: Theoretic |
I need some backup
Your teacher should have said that water doesn't wet wax because it's polar, so surface te ... |
24-10-2003 at 06:21
by: Theoretic |
nitroglycerin
Not that I actualy used the method, first I came up with the idea, then I searched the net. Nothing ... |
22-10-2003 at 06:32
by: Theoretic |
Deuterium toxicity
If lab animals are given D2O instead of H2O, they die, because, I think, deuterium-element bonds are ... |
17-10-2003 at 04:49
by: Theoretic |
Urea explorations
No, cyanides don't form at temperatures that low.
So, since urea and ammonium salts form guani ... |
15-10-2003 at 06:45
by: Theoretic |
nitroglycerin
What I wanted to say is just that the Ca(OH)2 method is more convenient for laboratory preparation, ... |
15-10-2003 at 04:37
by: Theoretic |
Sodium Synthesis
The mistake I see is using Al to dehydrate the NaOH. They react:
6NaOH+2Al=>2NaAlO2+2Na2O+3H2.
... |
15-10-2003 at 04:21
by: Theoretic |
nitroglycerin
By the way, if anyone is interested in how to get the precursor glycerine, it goes (supposedly) like ... |
14-10-2003 at 06:27
by: Theoretic |
Ammonium Nitrate and detonation
Well, by them, it's very easy to get AN to detonate (huh, chlorides! - mix AN with salt to deto ... |
13-10-2003 at 04:46
by: Theoretic |
Acidic water production...
I wonder what happens when a current with a voltage not big enough for electrolysis is run through, ... |
7-10-2003 at 06:31
by: Theoretic |
Ammonium Nitrate and detonation
"AMMONIUM NITRATE (NH4NO3)
SYNONYMS
None known.
CHARACTERISTICS
Colourless to white hyg ... |
6-10-2003 at 07:20
by: Theoretic |
The perfect explosive(s)
I was just thinking, could triazidoRDX (or even tetrazidoHMX) be prepared like this:
1)C3N3(NO2)3H3 ... |
3-10-2003 at 04:55
by: Theoretic |
HNO3????
Getting nitrites via the chloride route is impossible, NH4NO2 decomposes at low temperatures (hot wa ... |
3-10-2003 at 04:19
by: Theoretic |
HNO3????
An answer on the original question: H2O2 reacts with ammonia to give NH4NO2:
2NH3+3H2O2=>NH4NO2+ ... |
2-10-2003 at 07:27
by: Theoretic |
unconventional sodium
Not ionized? You mean floating around in clusters of anions and cations? Why would it dissolve then ... |
2-10-2003 at 04:30
by: Theoretic |
Making Nitrous Oxide
You mean NO and HNO3 and the like? Yes, they are formed, but not that much, otherwise a few members ... |
2-10-2003 at 04:24
by: Theoretic |
unconventional sodium
BUT!
"General
Synonyms: sodium acetate anhydrous
Molecular formula: CH3COONa
CAS No: 127- ... |
29-9-2003 at 06:16
by: Theoretic |
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