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Crc Handbook
Axehandle hasn't been very active lately, though, so you could try asking MadHatter via U2U also for ... |
25-1-2006 at 17:43
by: sparkgap |
can fictional chemicals have a real life counterpart?
Might BZ (quinuclidinyl benzilate) be the ticket to goblin's first question? I know it's a hallucino ... |
25-1-2006 at 06:24
by: sparkgap |
Book of the Organics
May I suggest either McMurry's or Carey's books? I have found them to be novice friendly. 
I do ... |
25-1-2006 at 06:20
by: sparkgap |
say goodbye to azeotropes!!
daeron, sure hope the company you are (or should I now say were?) working for doesn't come across th ... |
25-1-2006 at 06:15
by: sparkgap |
Having troubles identifying an unknown.
"...Piss yellow..." "...C6H12OH..." Why do I have the sickening feeling that your sample is conjugat ... |
18-1-2006 at 04:53
by: sparkgap |
Formation of polyhalide salt KICl4
I've made tetramethylammonium and tetraethylammonium polyiodide salts in the past (during my undergr ... |
13-1-2006 at 04:41
by: sparkgap |
Preparation of Grignard reagents...
Yes, the sodium press you speak off was mentioned in Vogel's.
[quote]
...The (sodium press) c ... |
26-12-2005 at 02:43
by: sparkgap |
Nitromethane extraction
"...Beware, nitronate is very flammable..."
I seem to remember that the reaction between nitromet ... |
26-12-2005 at 02:16
by: sparkgap |
Suspicious company
White phosphorus isn't worthless; it's just that the red allotrope is much safer to handle and use f ... |
26-12-2005 at 02:10
by: sparkgap |
Heterocyclic aromaticity
I no longer remember the exact numbers  , but I do remember that it was calculated
that the stabili ... |
8-12-2005 at 05:20
by: sparkgap |
Heterocyclic aromaticity
Only the electron pair in the pyrrole-like nitrogen of the imidazole ring participates in electron d ... |
8-12-2005 at 04:20
by: sparkgap |
OF3+ compounds
Does anyone here have access to Elsevier publications? I found a journal article that might answer P ... |
8-12-2005 at 01:38
by: sparkgap |
Acetic anhydride preparation
Maybe not disallowed, Magpie, but for me, I don't see the point of making acetic anhydride if you ha ... |
6-12-2005 at 20:52
by: sparkgap |
Question on making CH3NO2?
"Another thing I wondered, would diazotization be possible?"
It's possible, but gnarly. The resul ... |
6-12-2005 at 19:51
by: sparkgap |
phenethylbromide synthesis
rogue chemist, "fent" is the street shorthand for the potent opiate fentanyl.
I'd understand why ... |
6-12-2005 at 19:42
by: sparkgap |
nitropropene via nitromethane?
Uh, which of the three nitropropenes did you want? 1- and 2-nitropropene can't be prepared via a con ... |
4-12-2005 at 19:17
by: sparkgap |
Forum upgraded!
Most of the other forums I frequent use Invision, so I thought all other forum software implemented ... |
4-12-2005 at 04:31
by: sparkgap |
Forum upgraded!
If you take a look at the U2U panel, you'll note that there are supposed to be images there on the t ... |
4-12-2005 at 01:31
by: sparkgap |
Forum upgraded!
Nice. Maybe we can get a rolleyes smiley now?
I don't know... Whimsy topics show up in Today's ... |
3-12-2005 at 23:38
by: sparkgap |
Non-element organic shorthand
A useful link for those curious about chemical acronyms and abbreviations:
http://www.chemie.fu-b ... |
3-12-2005 at 03:25
by: sparkgap |
Distilling listerine....
Poloxamer 407 is a block copolymer of oxirane (ethylene oxide) and 2-methyloxirane (propylene oxide) ... |
30-11-2005 at 22:57
by: sparkgap |
Distilling listerine....
From [url=http://www.pfizerch.com/product.aspx?id=428]here[/url]:
[quote]
Active ingredients:
... |
30-11-2005 at 06:20
by: sparkgap |
Help me please !!!!!!! I need answer today :)
hexaaquoaluminum(III) would be the proper name for *THAT* complex ion.
sparky (~_~) |
30-11-2005 at 01:10
by: sparkgap |
Parared preparation
Mephisto,
May I suggest p-Dimethylaminoazobenzene, a.k.a. "Butter Yellow" the next time ... |
29-11-2005 at 08:34
by: sparkgap |
NH3-water azeotrope?
LeChatelier tells me that gaseous ammonia should be released when you boil ammonia water.
sparky ... |
29-11-2005 at 08:18
by: sparkgap |
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