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MEG
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 |
Hive
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
http://chemistry.about.com/library/weekly/aa040902a.htm
http://www.howstuffworks.com/light-stick4 ... |
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 |
Oops
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 |
Whoa
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 |
Flaming
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 |
Nope
[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 |
Replies:
Madscientist:
[quote]Nitration of 1-aminobenzene in mixed acid - I'm not sure if the nitration wi ... |
24-10-2002 at 13:35
by: PrimoPyro |
Hexanitrobenzene
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 |
Shit
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
Tired.......
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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