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thionyl chloride synthesis
This ties in very nicely with the chlorination of CS2 to make CCl4.
Because that reaction produce ... |
4-2-2009 at 06:57
by: Sauron |
To hissingnoise:
Yes, it's a recent pro model and I keep the firmware updated.
[Edited on 4-2-2009 by Sauron] |
4-2-2009 at 06:34
by: Sauron |
Alcohol from wheat
The inescapable fact is that we are using too much fossil fuel and so called alternative energy cann ... |
4-2-2009 at 03:30
by: Sauron |
On the subject of ORMUS
Don't waste your breath. The true believers will just curse you for a heretic and continue in their ... |
4-2-2009 at 02:37
by: Sauron |
thionyl chloride synthesis
It should be obvious to anyone reading the Inorg.Syn. article that the preparation of Cl2O in situ i ... |
3-2-2009 at 23:39
by: Sauron |
thionyl chloride synthesis
You continue to obfuscate, Len1, ZnCl2 is not the succesful catalyst in the benzotrichloride or HCMX ... |
3-2-2009 at 21:19
by: Sauron |
thionyl chloride synthesis
Also for those who prefer not to work with S2Cl2, CCl4 is a suitable replacement. I wonder whether ... |
3-2-2009 at 12:32
by: Sauron |
Alcohol from wheat
Automobile engines before the 1970s were capable of running on ethanol-water mixtures (no petrol) wi ... |
3-2-2009 at 10:09
by: Sauron |
On the subject of ORMUS
If I want to visit a fantasy world I'll go see LORD OF THE RINGS.
When I do science I do science ... |
3-2-2009 at 09:25
by: Sauron |
thionyl chloride synthesis
Len1's experiment with benzotrichloride was not supported by the literature. He did not employ any c ... |
3-2-2009 at 08:23
by: Sauron |
On the subject of ORMUS
Worth chucking out is more like it.
It;s all blather intended to fool the gullible and ignorant.
... |
3-2-2009 at 03:58
by: Sauron |
preparation of salicylic acid from anthranilic acid
In what country? |
3-2-2009 at 03:42
by: Sauron |
On the subject of ORMUS
The wise man picks his fights and does not fritter away his time and energies on trivialities like t ... |
3-2-2009 at 02:07
by: Sauron |
On the subject of ORMUS
The word is "misled"
No one needs to waste their time on this obvious chicanery. No one needs to ... |
2-2-2009 at 22:54
by: Sauron |
On the subject of ORMUS
This entire thread is an insult to everything that this forum is supposed to stand for. |
2-2-2009 at 19:10
by: Sauron |
On the subject of ORMUS
ZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZZNext stop: antigravity.
Bullshit! |
2-2-2009 at 08:33
by: Sauron |
On the subject of ORMUS
Hermes T. was right. This bullshit.
File this one next Red Mercury and the imaginary isotopes und ... |
2-2-2009 at 04:02
by: Sauron |
thionyl chloride synthesis
And the matching US patents
I had a go round with Len1 about this. He was pushing the oxidati ... |
1-2-2009 at 20:38
by: Sauron |
thionyl chloride synthesis
Read Kyrides. You do not need PCl5 to make phthaloyl chloride. You make it from phthalic anhydride a ... |
1-2-2009 at 20:24
by: Sauron |
thionyl chloride synthesis
Why not use CCl4 with sulfur instead of S2Cl2 to moderate the rxn w/ Cl2O?
The Cl2O producing rea ... |
1-2-2009 at 13:17
by: Sauron |
Practical Vacuum Distillation
Nope.
An aspirator (vacuum) pump is a metal or more usually plastic, inverted L-shaped device tha ... |
1-2-2009 at 04:23
by: Sauron |
thionyl chloride synthesis
That's for sure.
Jor told me he already has HgO.
He was going to make his own PCl5 from red P ... |
1-2-2009 at 02:05
by: Sauron |
thionyl chloride synthesis
CS2 is expensive and a fire hazard, combining something that flammable with a gas that is known to b ... |
1-2-2009 at 01:18
by: Sauron |
Practical Vacuum Distillation
That's the simplest possible setup for a vacuum distillation with no provision for fractionation.
... |
1-2-2009 at 01:05
by: Sauron |
thionyl chloride synthesis
I like this Cl2O reaction more and more. You need some S2Cl2 as solvent, which is reusable. You need ... |
31-1-2009 at 22:47
by: Sauron |
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