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Carboxylic acid -> Alkan
I tried this reaction once and the carboxylic acid was not reduced. I did a reflux and added all rea ... |
6-7-2007 at 04:40
by: chochu3 |
nitrostyrene
Organic Syntheses, Coll. Vol. 1, p.413 (1941); Vol. 9, p.66 (1929). has a few notes about this rxn.
... |
28-6-2007 at 22:17
by: chochu3 |
I need a cheap pH probe
Check out cynmar. Mightnot have that brand though, but may be interchangable. |
24-6-2007 at 15:01
by: chochu3 |
Is bracken fern carcinogenic when smoked?
Substances all have different vapor pressures, so when heated they go into gas form. They can be ove ... |
22-3-2007 at 23:07
by: chochu3 |
methylamine
Furch how did you work up the nitro reduction of nitromethane using iron and hydrochloric acid if yo ... |
16-2-2007 at 00:19
by: chochu3 |
post your favorite chemical reactions
[url=http://www.cci.ethz.ch/index.html]http://www.cci.ethz.ch/index.html[/url] has some nice expirem ... |
14-12-2006 at 19:50
by: chochu3 |
P2NP microwave crystallization problem
Its your nitroethane forming a salt with the sodium hydroxide if you search around you will find tha ... |
28-11-2006 at 19:01
by: chochu3 |
How did you find the Mad Science Discussion Board?
The HIVE |
12-10-2006 at 01:43
by: chochu3 |
After RXN how to extract aldehyde
sodium iodide I think can make a salt from an aldehyde. This may be found in Vogel's Pratical Chemis ... |
21-9-2006 at 02:33
by: chochu3 |
Bubbling ammonia gas into isopropanol
The old literature describes the procedure for using isopropanol as a solvent for birch reduction. |
12-9-2006 at 21:27
by: chochu3 |
What makes something able to accept NO2 groups?
pKa's also play factor in determining if NO2 will substitute or add unto a molecular substrate. |
13-6-2006 at 04:57
by: chochu3 |
fuckin plastic piece of shit hoses
That's why an authority always over checks the work of a techinician. |
13-6-2006 at 04:52
by: chochu3 |
Amphetamine via ephedrine?
It is possible as cherrybaby pointed out it can be used to reduce benzylic alcohol, but somethings w ... |
8-6-2006 at 22:52
by: chochu3 |
Reclaiming Iodine Crystals Does Not Work Why?
It dissipates, that's why they used to use the push/pull system.
[Edited on 1-6-2006 by chochu3] |
31-5-2006 at 20:44
by: chochu3 |
REQ: books on solid phase peptide synthesis
post in the correct thread. wanted books and references. |
23-5-2006 at 22:15
by: chochu3 |
books needed
post in the correct thread. wanted books and references. |
23-5-2006 at 22:15
by: chochu3 |
Nitrile to ketone? with EtMgBr
Are you asking for the mechanism or what is the product after 2,2-Diphenyl-3-methyl- 4-dimethylamino ... |
12-5-2006 at 23:21
by: chochu3 |
Imine Reduction with NaBH4
to reduce a carbonyl one could use wolf kishner reaction or clemmenson reaction. To get your ester b ... |
10-5-2006 at 03:54
by: chochu3 |
IMINE FORMATION
keep water out of the reaction as this reverses imine formation. You could boil with toluene in a de ... |
10-5-2006 at 03:50
by: chochu3 |
Michael addition
These type of reactions usally need to take out water by azetropic distillation for the reaction can ... |
10-5-2006 at 03:43
by: chochu3 |
HOW to control condition of experiment?
This can be controlled the same way as dienes can be, re-read up on thermodynamic and kinetic contro ... |
10-5-2006 at 03:21
by: chochu3 |
the most beautiful residue
neat |
29-4-2006 at 23:15
by: chochu3 |
Making Sodium Hydroxide (lye) ??
salt bridge will not dissolve because the solutions in each cell is saturated. |
22-4-2006 at 05:46
by: chochu3 |
Benzene Bromination
toluene forms an azetrope with water, so it could be the problem. |
10-4-2006 at 22:04
by: chochu3 |
books for students of pharmacy
Go to www.avaxhome.ru and type in pharmacy their. |
8-4-2006 at 20:03
by: chochu3 |
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