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Manganese Carbonate
Hold on. Way safer way to make it without chlorine. Mix and acid and H2O2 and MnO2. H2O2 will be ... |
8-7-2006 at 12:31
by: guy |
Are NaOH and KOH Interchangeable for Basification?
Why the heck do people still use mass percent? Molarity is so much better. Everyone one on earth s ... |
7-7-2006 at 20:13
by: guy |
Carboxylic acid strengths
Hey how come HClO is weaker than HCl. I think it is because the O is less withdrawing because it al ... |
6-7-2006 at 22:23
by: guy |
Mechanism of Permanganate/oxalate reaction
Does anyone have any idea how this reaction works? I found an online journal (ACS) but I didn't hav ... |
6-7-2006 at 21:10
by: guy |
Decomposition of sulfamate
Well to from ammonia, one of the hydrogen has to break of from another -NH2, and don't see why it wo ... |
5-7-2006 at 11:47
by: guy |
i need sulfer
Those are two very different things. Sulfur can be found in some gardening stores, and in some smal ... |
4-7-2006 at 17:14
by: guy |
Decomposition of sulfamate
I don't see how ammonia could have possibly be produced from a sulfamate. The nitrogen has to be oxi ... |
3-7-2006 at 17:16
by: guy |
Decomposition of sulfamate
Well I decomposed some Ferric sulfamate today. I gave of white fumes of gas (but not like ammonium s ... |
3-7-2006 at 15:47
by: guy |
Higher oxidation states of caesium.
There's no way to form anions of noble gases because there is not enough affinity for the electron w ... |
30-6-2006 at 18:10
by: guy |
Acetaldehyde synthesis
That's probably why drinking IS bad for you. 
http://www.reboundhangover.com/acetaldehyde.htm |
30-6-2006 at 17:46
by: guy |
Decomposition of sulfamate
How is the hydrogen on the N reducing? If anything it should be oxidizing. I imagine that the N--S ... |
30-6-2006 at 17:21
by: guy |
Decomposition of sulfamate
I searched google and found that salts of sulfamic acid produce NOx and SOx. Is this possible becau ... |
30-6-2006 at 13:26
by: guy |
H2SO4 consentration for esters?
Just wondering, how come 3% H2O2 works just as fine as concentrated H2O2 for AP synthesis? Water is ... |
30-6-2006 at 11:44
by: guy |
H2SO4 consentration for esters?
Concentrated acid is used. All the other reactants are usually very pure without a lot of water. I ... |
29-6-2006 at 18:45
by: guy |
Synthesis of 2 Chloropropane?
Is it possibe to just use isopropyl alcohol and HCl to form isopropyl chloride by nucleophilic subsi ... |
28-6-2006 at 19:54
by: guy |
Synthesis of 2 Chloropropane?
The best choice is propene. The H+will attack the double bond as a electrophile, and the the Cl- wi ... |
28-6-2006 at 18:18
by: guy |
Weird compound
No you can make ethyl acetate from hypochlorite. See here http://www.erowid.org/archive/rhodium/che ... |
24-6-2006 at 14:07
by: guy |
Weird compound
About a week ago I made some ethyl acetate by sodium hypochlorite and ethanol. Then I added some am ... |
24-6-2006 at 12:43
by: guy |
Cobalt Chloride
[quote]
Hydrogen peroxide is a reducing agent here? I always saw it as an oxidizing agent in this t ... |
22-6-2006 at 14:13
by: guy |
Cobalt Chloride
Yea sure you can get cobalt chloride by dissolving the hydroxide or carbonate. If it is Co(III) hyd ... |
20-6-2006 at 22:51
by: guy |
Alkylamines via gas phase alkylation
Why use AlCl3, use Al2O3 it is more stable at higher temperatures. And how will you prevent the amm ... |
18-6-2006 at 10:29
by: guy |
CaHPO4
Try to see how much acid is needed to dissolve it, forming Ca(H2PO4)2 which is soluble. |
8-6-2006 at 16:41
by: guy |
pH
Yeah I figured it out |
8-6-2006 at 14:13
by: guy |
Question on making CH3NO2?
O I see now. For some reason I was thinking the carbon had a negative charge, duh.
Then how does ... |
7-6-2006 at 19:26
by: guy |
Question on making CH3NO2?
Wouldn't a nitration produce a nitro compound, not a nitrite ester? But anyways I found the answer, ... |
7-6-2006 at 18:54
by: guy |
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