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Nicotine Extration. (At Home) you know I already explained to you via U2U how to purify this, using methods that are doable at hom ... |
4-2-2012 at 16:03 by: ThatchemistKid |
Nicotine Extration. (At Home) Well, you lucked out the PKa of one of the nitrogens on nicotine is 8.1 and the Pka of citric acid f ... |
4-2-2012 at 09:41 by: ThatchemistKid |
Calcium acetate + hydrogen peroxide will give acetone peroxide http://www.chemguide.co.uk/organicprops/alcohols/oxidation.html
well here is a standard start
mayb ... |
2-2-2012 at 22:12 by: ThatchemistKid |
Calcium acetate + hydrogen peroxide will give acetone peroxide Vikascoder, you seem to be asking to be spoon fed about how to make explosives, and showing that you ... |
2-2-2012 at 08:16 by: ThatchemistKid |
Preparation of Styrene and Phenylacetylene from Polystyrene I preformed this scheme a few months ago, though I stopped at the dibromo compound, grad school now ... |
1-2-2012 at 22:17 by: ThatchemistKid |
Change wavelength of light? Maybe this will give you a couple of ideas, I do not know much about this so here is my 2 cents
h ... |
1-2-2012 at 17:46 by: ThatchemistKid |
Calcium acetate + hydrogen peroxide will give acetone peroxide I would think that if anything it would make peroxy acetic acid.
so If you feel like doing some epo ... |
31-1-2012 at 08:54 by: ThatchemistKid |
A small quantity of gallium available for interest Do you ship to the US? |
22-1-2012 at 09:01 by: ThatchemistKid |
Benzaldehyde + Dimethylether => 3-methoxybenzaldehyde? First off you are suggesting that the protonated positively charged ether will be attacked by the be ... |
20-1-2012 at 11:56 by: ThatchemistKid |
Acetylene + 2-propanol both my graduate organometallic courses ( one taught by an inorganic chemist and one taught be an or ... |
15-1-2012 at 17:34 by: ThatchemistKid |
Acetylene + 2-propanol Foot in mouth! actually you can form that product from those reactants using chemistry known as Repp ... |
15-1-2012 at 11:03 by: ThatchemistKid |
Acetylene + 2-propanol I Cannot figure out a mechanism or conditions to make that work, I searched through some radical rea ... |
15-1-2012 at 10:57 by: ThatchemistKid |
Tert-Butyl Lithium "tertiary-alcohol based organolithium reagent", you stated a specific one was mentioned just out of ... |
9-1-2012 at 14:20 by: ThatchemistKid |
Substituting transitional metal catalysts if yields were all in the 95% range they would have most certainly reported it. I doubt that your th ... |
7-1-2012 at 19:03 by: ThatchemistKid |
A puzzle from the Mitsunobu reaction Are you sure the DIAD is not a solution of 40% concentration in toluene...generally from what I have ... |
25-12-2011 at 11:33 by: ThatchemistKid |
Most extreme compounds known to man Dicyanoacetylene, highest flame temp achieved by burning an organic compound when it is burned with ... |
21-12-2011 at 21:35 by: ThatchemistKid |
Reaction of 1-Phenyl-2-chloropropane with methylamine? I think i found an answer, check M6[?]
http://docs.google.com/viewer?a=v&q=cache:joLPGiYqausJ:w ... |
21-12-2011 at 16:49 by: ThatchemistKid |
Oxidation of Isopropanol You will get oxidation of the alcohol to acetone with that reaction but it will not stop there you w ... |
8-12-2011 at 22:27 by: ThatchemistKid |
Allyl chloride (bromide) The first part did come from orgsynth, I have used that procedure before in an attempt to make allyl ... |
21-11-2011 at 12:19 by: ThatchemistKid |
Protein Kinase A / Pyruvate Kinase Regulation Confusion I see how this is confusing, I could not see the reason why this occurred either. You are missing a ... |
12-11-2011 at 08:35 by: ThatchemistKid |
Chloroform -> Formic Acid The reaction between chloroform and NaOH Intially forms the trichloromethyl anion but that quickly c ... |
11-10-2011 at 09:10 by: ThatchemistKid |
Sodium chloride when using hydrogen chloride This drivel about atomic orbitals was me sick and delusional last night, Luckly I am feeling better. ... |
9-10-2011 at 17:51 by: ThatchemistKid |
Sodium chloride when using hydrogen chloride I am a little sick at the moment, and maybe not thinking clearly, but I was wondering about electron ... |
8-10-2011 at 19:38 by: ThatchemistKid |
Removal of alkyl ramifications Well, I think probably the easiest way in the situation with xylene or toluene would be the oxidatio ... |
5-10-2011 at 10:10 by: ThatchemistKid |
A new solvent from a nailpolish remover It could be a complicated mixture of things, I have seen nail polish removers contain a mixture of b ... |
2-10-2011 at 11:05 by: ThatchemistKid |
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