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NH3 gas + CuCl2....preciptate at first..but then dissapears...why?
Read up on coordination compounds. |
16-12-2007 at 15:13
by: guy |
Very large needles in my H2SO4/KNO3 mix?
KNO3 is needle shaped. You probably dissolved a large amount of KNO3 when the solution was hot from ... |
4-12-2007 at 23:21
by: guy |
Coordination chemistry of nickel(II)
If you can get any phosphite esters or triphenylphosphine, you can make Ni(0) complexes which are us ... |
4-12-2007 at 23:18
by: guy |
Substitution reactions (Alkyl Halide)
Iodine is not strong enough to oxidize a C-H bond |
26-11-2007 at 19:14
by: guy |
Oxidation of metals by acids
What is the 'mechanism' for the oxidation of metals by protons? I ask because I am trying to figure ... |
24-11-2007 at 19:02
by: guy |
Substitution reactions (Alkyl Halide)
You better shine some UV light on the chlorination reaction. That is the only way Cl2 can react with ... |
24-11-2007 at 11:38
by: guy |
FA polymerization
As you can see, furfural has a nice aldehyde, which when protonated is a good electrophile. Then the ... |
24-11-2007 at 11:30
by: guy |
Fun Reactions from Houshold Reagents
Wow that Copper(II) - dichlorocyanurate compound looks awesome |
22-11-2007 at 23:59
by: guy |
Secondary and benzylic alcohols oxydations using various oxydants
[quote][i]Originally posted by Klute[/i]
How much triacetoneamine did you roughly obtain?[/quote]
... |
22-11-2007 at 16:23
by: guy |
Secondary and benzylic alcohols oxydations using various oxydants
Unfortunately at the time I didn't have any Oxone. |
22-11-2007 at 14:58
by: guy |
Secondary and benzylic alcohols oxydations using various oxydants
Preparation of Triacetoneamine(4-Oxo-2, 2, 6, 6-tetramethylpiperidine), an Improved Method
G SOSNO ... |
20-11-2007 at 16:59
by: guy |
Secondary and benzylic alcohols oxydations using various oxydants
I wasn't really sure. Nicodem said it was a yellow liquid but all other sources say its a solid.
... |
20-11-2007 at 13:13
by: guy |
OTC PTC (Phase Transfer Catalysts)
Pool algaecide has a lot of quat salts. They also add a dye though. |
18-11-2007 at 23:33
by: guy |
Moving to New Orleans in Spring... Good Schools?
What about Tulane which is in New Orleans?
Emory University is in Atlanta |
18-11-2007 at 19:03
by: guy |
Lead Nitrate
NO because lead sulfate will precipitate out |
18-11-2007 at 16:17
by: guy |
Storage of Di-ethylether
[quote][i]Originally posted by Centimeter[/i]
You asked how these explosive properties are evolved ... |
18-11-2007 at 15:01
by: guy |
Secondary and benzylic alcohols oxydations using various oxydants
[quote][i]Originally posted by Klute[/i]
Thanks for the link not_important, speaking of TEMPO, my 2 ... |
18-11-2007 at 14:22
by: guy |
Secondary and benzylic alcohols oxydations using various oxydants
For reactions using TCCA/ KBr ...Im assuming the active species formed is BrO-. Why is BrO- better ... |
15-11-2007 at 19:29
by: guy |
Oxidation of tartaric acid
Ok Thanks. Ethylene glycol is easy to get.
Alkaline KMnO4 can do the job...but I would like to kno ... |
8-11-2007 at 21:04
by: guy |
Oxidation of tartaric acid
@Sauron,
I see...do you know of any good oxidizer that can oxidize it to oxalic acid that will n ... |
8-11-2007 at 13:25
by: guy |
Oxidation of tartaric acid
Is it possible to oxidize tartaric acid with some mild oxidizing agent to either glyoxal or oxalic a ... |
8-11-2007 at 00:25
by: guy |
mechanism of benzoic acid formation from butyl lithium
Are you sure those are all of the steps?
The only thing that is possible is the formation of 1-Bu ... |
30-10-2007 at 21:53
by: guy |
Good book on bonding theory?
FYI, hybridization is not really how bonding works, its just useful for predicting geometries of org ... |
30-10-2007 at 15:48
by: guy |
Is MSG useful for anything?
I mixed it with NaOH soln and I definitely got an ammonia smell.
I guess this is pretty consisten ... |
17-10-2007 at 20:00
by: guy |
Is MSG useful for anything?
I used Fehling's test and got no results. I think this may be 3-cyanopropanoic acid. I think the c ... |
17-10-2007 at 17:43
by: guy |
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