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Ever read about the MEG? Very controversial, many people don't believe it works even with poor ...
29-10-2003 at 23:26
by: PrimoPyro
Try using the search engine at the Hive for this topic, in the serious chem forum.

I know it has ...
8-11-2002 at 19:30
by: PrimoPyro
What the hell?
Why does this board add characters out of nowhere every time I post a url? this "/>" character makes ...
3-11-2002 at 20:06
by: PrimoPyro
Search ...
3-11-2002 at 20:04
by: PrimoPyro
Of Course
And you are right, I was only being sarcastic. N2O5 could be put to much better use than nitration, ...
2-11-2002 at 06:53
by: PrimoPyro
Thats why you dont use HNO3 :P
Thats why you use N2O5 as the nitrating agent. Yields are better, but there are more side reactions ...
1-11-2002 at 19:45
by: PrimoPyro
The procedure is valid, but I stated the wrong catalyst. It is Zn(CN)2 not CuCN, sorry. Where I got ...
30-10-2002 at 04:53
by: PrimoPyro
I dont understand
I dont understand your question. Could you re-word it please?
28-10-2002 at 15:07
by: PrimoPyro
Urushibara Nickel + H2
Prepare precipitated nickel from NiCl2 via Urushibara methods, and use either H2 or ammonium formate ...
28-10-2002 at 15:02
by: PrimoPyro
AlB12 wouldn't that be um 'good' for thermite fuel?

Is it especially dense?
27-10-2002 at 13:49
by: PrimoPyro
Alkalai Aluminum Hydrides
Well, what about Fe3O4 and KAlH4? (shiver in fear at the thought of its sensitivity)

That should ...
27-10-2002 at 13:46
by: PrimoPyro
Unless that was some weird personal inside joke between the two of you, that was highly uncalled for ...
26-10-2002 at 03:56
by: PrimoPyro
[quote]Start with p-DCB mothballs, nitrate as much as you can, then reflux with NH3, then nitrate mo ...
25-10-2002 at 14:12
by: PrimoPyro

[quote]Nitration of 1-aminobenzene in mixed acid - I'm not sure if the nitration wi ...
24-10-2002 at 13:35
by: PrimoPyro
Would be pretty strong wouldn't it? One would think so. But hard to prepare. Couldn't be done by nit ...
24-10-2002 at 06:21
by: PrimoPyro
That is sooo vague though
There are billions of types of plastic. Also note that some of these must be imperveous to alcoholic ...
24-10-2002 at 01:12
by: PrimoPyro
Mechanics of Aromatic Diazotization (with diagrams!)
1.I dont have an O-chem teacher. I am self taught and have yet to go to professional school.

2.I ...
22-10-2002 at 03:45
by: PrimoPyro
ClO- ?
Where are you getting hypochlorite ions in solution from? Am I missing something?

For the synthes ...
21-10-2002 at 13:17
by: PrimoPyro
Starter Fluid
Go to Thrifties/Rite-Aid/Walmart, etc.

Get the aerosol engine starter fluid that contains diethyl ...
20-10-2002 at 17:33
by: PrimoPyro
Acidic Medium
Yes, as was shown in my mechanism for diazotization thread, O=N-Cl is made by protonation and dehydr ...
20-10-2002 at 17:20
by: PrimoPyro
Man, my fatigue is making me stupid, lol. I forgot to link the picture, doh!

It would [i]really[/ ...
20-10-2002 at 06:49
by: PrimoPyro
Mechanism: N2H4 + NaNO2 ----> NaN3 + 2H2O

Detailed explanation to come in a couple hours, after some sleep. Wanted to get this ...
20-10-2002 at 06:47
by: PrimoPyro
Damn man.....
WTF is up lately??

These threads all seem so active, and then I make a post and they die instantl ...
9-10-2002 at 04:03
by: PrimoPyro
Hm I wonder
I wonder if concentrated solutions of HCl and KHSO4 could cause the following reaction, which is hig ...
8-10-2002 at 03:30
by: PrimoPyro
I doubt it
It sounds to me like what happened was you polymerized your acetone with the HCl, and then depolymer ...
8-10-2002 at 03:25
by: PrimoPyro
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