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ONTA
There's still a mistake in figure 1 - you've drawn an sp2 hybridised carbon without a 180* bond angl ... |
8-8-2006 at 07:25
by: Nick F |
The Ultimate Energetic Compound
Please, do some reading. TeNM is often discussed. |
1-8-2006 at 17:28
by: Nick F |
ONTA
NTO is easier. Nitrourea reduction with acid/Zn, followed by precipitation of the semicarbazide prod ... |
31-7-2006 at 07:17
by: Nick F |
Idea for bottling chlorine...
Has anyone ever made any liquid chlorine? I was thinking about making some and ampouling it next tim ... |
24-7-2006 at 15:23
by: Nick F |
Super-Containment?
Yeah, you don't want to be using cast, and you might like to try more than a lb of steel if you're u ... |
21-7-2006 at 06:37
by: Nick F |
Super-Containment?
Reminds me of something interesting I learned a little while back.
If you mix hydrogen and oxygen i ... |
20-7-2006 at 12:34
by: Nick F |
Electrolytic Nitration
Ethene may be hard to buy, but it's easy to make.
Everything I've read suggests that these types ... |
20-7-2006 at 12:25
by: Nick F |
Ethyl amine from Acetonitrile
Acid catalysis will tend to result in acetic acid. After protonation of the nitrogen, you'll still n ... |
20-7-2006 at 12:18
by: Nick F |
Enolate Alkylation
Well...
Low temperatures and strong bases will favour the kinetic enolate, ie, deprotonation from ... |
19-7-2006 at 11:21
by: Nick F |
How can I get started?
Ebay can be surprisingly good for standard lab equipment. You can find some nice chemicals as well.. ... |
18-7-2006 at 13:33
by: Nick F |
doubt about benzene
It is unsaturated, but aromatic. This aromaticity stabilises the molecule by ~150 kJmol-1, which acc ... |
18-7-2006 at 05:16
by: Nick F |
How can I get started?
What do you mean by "study"? What do you want to do? To say that you want to study "gases," an entir ... |
15-7-2006 at 17:01
by: Nick F |
How can I get started?
Books. |
15-7-2006 at 11:11
by: Nick F |
ethyl rocket motors
Lol, when I was younger one of my favourite mixtures was potassium permanganate with red phosphorus ... |
14-7-2006 at 09:24
by: Nick F |
Carboxylic acid strengths
Yeah, I've had both Keeler and Wothers as lecturers, they are very good at explaining things and I i ... |
9-7-2006 at 16:46
by: Nick F |
Anyone interested in sulfur nitride?
I haven't studied it very much. I had a lecture course on p-block inorganic rings, chains and networ ... |
7-7-2006 at 05:58
by: Nick F |
Carboxylic acid strengths
I actually used to hate physical organic chemsitry, but the more I learn, the more interesting it be ... |
6-7-2006 at 14:51
by: Nick F |
Carboxylic acid strengths
Hehehe  .
To be fair, it would have taken me a very long time to come up with the answer if I ha ... |
6-7-2006 at 14:40
by: Nick F |
Carboxylic acid strengths
Rogue: that has an effect, but it is not the major one  .
Not so easy!!
Edit: your clue is th ... |
6-7-2006 at 03:30
by: Nick F |
Carboxylic acid strengths
Here's an interesting question, let's see if anyone gets it :
Why is trichloroacetic acid abou ... |
5-7-2006 at 15:46
by: Nick F |
Anyone interested in sulfur nitride?
"Yes I am very interested and not so much for its explosive properties, rather
for it's properties ... |
5-7-2006 at 12:52
by: Nick F |
Tetramethylenehexaamine
Look at DABCO (1,4-diazo[2.2.2]bicyclooctane), for example. pKaH of diprotonated DABCO is 3.0, that ... |
30-3-2006 at 18:56
by: Nick F |
Dissolving Radium and Friends
Hey, I'm doing the same thing myself! Mainly because I want some radium, although if I can get enoug ... |
28-3-2006 at 19:34
by: Nick F |
Naphthol anologs of TNP
Nitration of napthalene at lower temperatures gives 1-nitronapthalene due to kinetics, since the car ... |
27-3-2006 at 11:07
by: Nick F |
nitration without sulfuric acid
But they can lead to (potentially dangerous) side reactions. |
25-1-2006 at 15:52
by: Nick F |
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