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Sodium carbonate? That won't work. However, you can convert sodium bicarbonate into sodium carbonate by heating o ... |
11-4-2003 at 13:41 by: madscientist |
Separatory Funnel What are you trying to separate? I'm not sure I quite understand what exactly the problem is yo ... |
11-4-2003 at 13:35 by: madscientist |
DNP -A great fatburner The body reduces the nitro groups, but nothing more. |
9-4-2003 at 04:29 by: madscientist |
new ernergetic materials Nick, you should try oxidizing the amino group in your 5-aminotetrazole to a nitro group, ozone bein ... |
7-4-2003 at 14:37 by: madscientist |
Mr. Anonymous: HgCl2 prep Mr. Anonymous, sodium polysulfide should work for arresting the rapid oxidation process of reactive ... |
7-4-2003 at 12:41 by: madscientist |
Power Source Several years ago, I electrolyzed a sodium chloride solution with wall current (as in, what Darkfire ... |
2-4-2003 at 20:34 by: madscientist |
Acetic anhydride, the 2nd. The seemingly ancient post to which I was referring to:
[quote]I'm not sure, but I think tha ... |
2-4-2003 at 20:17 by: madscientist |
Acetic anhydride, the 2nd. I'm guessing that what would happen with a SO<sub>3</sub>/acetic acid heating proce ... |
2-4-2003 at 13:16 by: madscientist |
Inert material in M-80 style firecrackers? It definitely is possible. Take me, for example. I'm sixteen and am breezing my way through a c ... |
2-4-2003 at 09:43 by: madscientist |
Readily Available Chemicals Website According to the organic chemistry textbook used by Princeton University, phenyl azide is also used ... |
2-4-2003 at 09:35 by: madscientist |
ICE-Advantages of N2O over O2 My guess would be that it has to do with the highly exothermic formation of N<sub>2</sub> ... |
31-3-2003 at 21:30 by: madscientist |
The Pet Store How much (as in, volume) of that formalin solution does $9.99 buy? |
27-3-2003 at 10:11 by: madscientist |
Benzene synthesis The third nitration of mesitylene is what makes it dangerous - it must not be conducted at elevated ... |
26-3-2003 at 13:23 by: madscientist |
Ni from coins The coins are Cu/Ni alloys though; and Cu/Ni alloy requires higher pressures/temperatures for the fo ... |
25-3-2003 at 19:43 by: madscientist |
Extracting Phosphorus from P2O5. White phosphorus and red phosphorus are both forms of elemental phosphorus (called allotropes). Whit ... |
19-3-2003 at 09:38 by: madscientist |
zincdust I would finely powder your ZnO and CaC<sub>2</sub>, mix as intimately as possible, and s ... |
19-3-2003 at 09:27 by: madscientist |
Ni from coins I've actually made efforts at isolating nickel from American nickels (which are made from a 25% ... |
18-3-2003 at 18:26 by: madscientist |
zincdust It would be a fuel/oxidizer reaction, as in:
3ZnO + CaC<sub>2</sub> ----> CaO + 2C ... |
17-3-2003 at 16:39 by: madscientist |
Nicotine Nitrated nicotine won't have unusually good explosive properties - I assume that's what th ... |
14-3-2003 at 13:56 by: madscientist |
formaldehyde from methanol Some CH<sub>2</sub>O should bubble out; bubble that into water and you'll get aqueo ... |
14-3-2003 at 13:53 by: madscientist |
substitution and oxidation Could you provide structural formulas, and state what "X" stands for? |
12-3-2003 at 19:06 by: madscientist |
Crazy Benzene-synthesis Ball and stick models may look pretty, but they're too cumbersome to be used for diagramming re ... |
12-3-2003 at 13:33 by: madscientist |
Crazy Benzene-synthesis You might want to consider downloading "ISIS Draw" for diagramming organic reaction scheme ... |
10-3-2003 at 17:53 by: madscientist |
Usability of Atmospheric Nitrogen The problem has to do with the extremely strong nitrogen-nitrogen triple bond in the diatomic N<s ... |
3-3-2003 at 15:59 by: madscientist |
Direct Esterification of Phosphoric Acid It probably would be possible to yield the dialkyl ester via direct esterification, but not the tria ... |
3-3-2003 at 15:51 by: madscientist |
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