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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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