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Heating element temperatures?
[rquote=220325&tid=17372&author=Acetic Acid]What are the normal temperatures for some common ... |
27-8-2011 at 17:02
by: redox |
Phenol From Glow Sticks
[rquote=220315&tid=17354&author=ab5000]Making it from Aspirin tablets is simplier.
First, e ... |
27-8-2011 at 12:28
by: redox |
Benzyl Alcohol -> Benzaldehyde via Silica Gel Supported Jones Reagent
[rquote=220257&tid=6671&author=questions]Our friend "cyclonknight" described an attractive p ... |
27-8-2011 at 08:01
by: redox |
cinnamon oil to benzaldehyde
A concentrated solution of NaOH will in fact disproportionate aldehydes. However, this is by far not ... |
27-8-2011 at 06:59
by: redox |
Thermite problem
[rquote=220232&tid=17369&author=labworm]I've tried to make thermite, using a VERY fine alumi ... |
26-8-2011 at 14:59
by: redox |
Lab Safety
[rquote=220231&tid=17339&author=MeSynth]FUME HOOD | GOGGLES/GLASSES AND A FACE SHIELD | GLOV ... |
26-8-2011 at 14:49
by: redox |
Synthesis of malonic acid
[rquote=219985&tid=1600&author=querjek]I'm not too sure if this pathway would work--what abo ... |
26-8-2011 at 07:06
by: redox |
Grease sources for glassware joints?
[rquote=220190&tid=17312&author=MeSynth]Like I said before lube is not needed unless your gl ... |
26-8-2011 at 06:48
by: redox |
Preparation of Sodium Nitrite NaNO2
[rquote=220178&tid=16941&author=Chemistry Alchemist]Heating up Nitrates make them loose a ox ... |
26-8-2011 at 06:37
by: redox |
Grease sources for glassware joints?
[rquote=220161&tid=17312&author=CuriosityKilledtheKat]here is a website that teaches you how ... |
25-8-2011 at 19:49
by: redox |
S02 gas
Is there a specific reason why ammonium chloride allows lower temperatures than, say, sodium chlorid ... |
25-8-2011 at 12:40
by: redox |
S02 gas
[rquote=220122&tid=17348&author=White Yeti]Solution to these problems: liquefying the gas en ... |
25-8-2011 at 10:40
by: redox |
Phenol From Glow Sticks
Isn't this the [i]fourth [/i] topic you have started today? Whatever, it doesn't matter.
I was un ... |
25-8-2011 at 08:09
by: redox |
Lithium from Batteries
[rquote=220070&tid=17352&author=blogfast25]
Lemmesee, so you’re going to extract some Li ... |
25-8-2011 at 07:21
by: redox |
S02 gas
One disadvantage for burning sulfur to generate SO2 is the fact that it is difficult to lead the SO2 ... |
25-8-2011 at 06:23
by: redox |
S02 gas
You can generate sulfur dioxide by the reaction of sulfite, bisulfite, or metabisulfite salts with a ... |
24-8-2011 at 18:40
by: redox |
Extract of Benzene thread
[rquote=219998&tid=4902&author=MeSynth][rquote=180101&tid=4902&author=white rabbit]I ... |
24-8-2011 at 17:33
by: redox |
Make Potassium (from versuchschemie.de)
Toluene as a solvent? It boils a 110 or so. That is [i]much[/i] too low a temperature for this react ... |
24-8-2011 at 09:16
by: redox |
Toluene Directly to Benzene?
Somewhere there was a thread about benzene production that detailed the freidel-crafts method, just ... |
24-8-2011 at 09:14
by: redox |
Nitromethane, Nitro methanol and Methyl nitrate !!
No, No, that's not what I mean. I know that a nitro group on an oxygen is then nitrate. I'm asking i ... |
24-8-2011 at 08:47
by: redox |
Nitromethane, Nitro methanol and Methyl nitrate !!
Well, yeah, but does nitromethanol exist? Can a nitro group be on the same carbon as a hydroxyl? I h ... |
24-8-2011 at 08:20
by: redox |
Nitromethane, Nitro methanol and Methyl nitrate !!
How come a nitro group cannot be on an alcohol? |
24-8-2011 at 08:09
by: redox |
Toluene Directly to Benzene?
You could try a friedel-crafts dealkylation disproportionation reaction. One could combine toluene w ... |
24-8-2011 at 08:02
by: redox |
Nitromethane, Nitro methanol and Methyl nitrate !!
The first picture is nitromethane. It is a nitroalkane.
The second picture is nitromethanol. It ... |
24-8-2011 at 07:54
by: redox |
Isobutyl Nitrite
[rquote=219913&tid=5598&author=sonottawa][rquote=219154&tid=5598&author=redox][rquot ... |
24-8-2011 at 05:42
by: redox |
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