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Preparation of ethylene
That is great to hear that the Al2O3/EtOH method works. I have a few questions though:
*How shou ... |
9-11-2006 at 13:18
by: guy |
Preparation of ethylene
I can probably purify it by absorbing most of the ethylene in a solution of [CuCl2]-.
Would thi ... |
8-11-2006 at 23:42
by: guy |
Preparation of ethylene
I'm not sure if there is already a thread on this, but I was wondering if anyone has ever made ethyl ... |
8-11-2006 at 17:24
by: guy |
Ozone perhaps?
I don't think you need Cu(NO3)2 in there, its just ClO2 gas from chlorate and acid. ClO2 probably c ... |
8-11-2006 at 12:51
by: guy |
HF and SrTiO3
You might not want to work with HF.
NaOH will do just fine, you will need to heat it though. |
8-11-2006 at 12:47
by: guy |
addition to alkenes
[quote][i]Originally posted by Sandmeyer[/i]
Damn, I wish I went to scool in America, they actually ... |
6-11-2006 at 20:53
by: guy |
addition to alkenes
[quote][i]Originally posted by Drunkguy[/i]
Actually, 4 is (b). [/quote]
Why would 4 be B? It w ... |
5-11-2006 at 18:06
by: guy |
addition to alkenes
2 - A, markinokov rule
9 - C? |
5-11-2006 at 12:46
by: guy |
High Yield Alcohol Chlorination Using Chloroform
Alcoholic hydroxide with chloroform makes mostly CO, C2H4, HCOO-. Those gases explain the vigourous ... |
3-11-2006 at 19:25
by: guy |
Fe(CO)5 and it's orbitals
No,because you have to follow the 18 electron rule, and plus, CO bonds are known for their pi backbo ... |
1-11-2006 at 11:42
by: guy |
High Yield Alcohol Chlorination Using Chloroform
Whatever it was, it was very exothermic and vigorous producing an orange color imediately with lots ... |
31-10-2006 at 23:55
by: guy |
High Yield Alcohol Chlorination Using Chloroform
http://pubs.acs.org/cgi-bin/abstract.cgi/jacsat/1971/93/i07/f-pdf/f_ja00736a064.pdf?sessid=6006l3
... |
31-10-2006 at 22:42
by: guy |
Fe(CO)5 and it's orbitals
Alright I think I got it figured out.
Fe(CO)5 has 4 pi bonded CO and one sigma bonded CO(followin ... |
31-10-2006 at 18:00
by: guy |
Fe(CO)5 and it's orbitals
Are you doing ligand field theory, or just simple coordiation complexes without MO theory? |
31-10-2006 at 13:59
by: guy |
Fe(CO)5 and it's orbitals
I think its because of pi backbonding, it interacts with only the dxy dxz and dyz, and fills it up w ... |
31-10-2006 at 13:13
by: guy |
HCN by chloroform and ammonia in base
YEs! I finally did it. At first I was mixing only a little of the cyanide solution in so I didnt ge ... |
31-10-2006 at 12:02
by: guy |
HCN by chloroform and ammonia in base
Wow, it seems I just have bad luck. Ill follow you procedure exactly tommorow and hope to get some ... |
30-10-2006 at 20:19
by: guy |
HCN by chloroform and ammonia in base
So I tried it again today. I didnt get it to work the Prussian blue test (I mixed the solution with ... |
30-10-2006 at 18:34
by: guy |
an inorganic chemistry mystery
[quote][i]Originally posted by Dr. Beaker[/i]
if you want something to be ionized you need the ions ... |
29-10-2006 at 15:18
by: guy |
an inorganic chemistry mystery
I dont see why it cant be an SN1 equivalent. Cl- are constantly in equilibrium, moving in and out o ... |
29-10-2006 at 14:03
by: guy |
Methane Hydrate
Have you seen the show Mythbusters?
Theres this episode where they did many KEWL experiments but ... |
27-10-2006 at 15:56
by: guy |
HCN by chloroform and ammonia in base
I used NaOH and (NH4)2SO4 to generate the gas. I think when water is present a phase transfer catal ... |
26-10-2006 at 15:29
by: guy |
HCN by chloroform and ammonia in base
I have a question, for the reaction with the quaternary ammonium salts, will 10% ammonia solution wo ... |
26-10-2006 at 15:14
by: guy |
HCN by chloroform and ammonia in base
[quote][i]Originally posted by Polverone[/i]
It is plausible and I have done it, confirmed by the p ... |
25-10-2006 at 21:13
by: guy |
HCN by chloroform and ammonia in base
I was thinking about bubbling gaseous ammonia into the solution. Actually the cyanide salt is what ... |
25-10-2006 at 11:29
by: guy |
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