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carboxylic acid functional group
Why do you reply to threads you have not even bothered reading first?  |
18-10-2007 at 09:35
by: Nicodem |
carboxylic acid functional group
Still that is not a mechanism. And the solvent used must be aprotic and not an acid. Besides it was ... |
18-10-2007 at 09:31
by: Nicodem |
KOCN
If you have some primary or secondary amine, or an aniline, you can do a primitive organic test (tho ... |
17-10-2007 at 10:27
by: Nicodem |
Choosing a research article for discussion
Just check the latest three issues of the top journals from the field your presentation is supposed ... |
17-10-2007 at 10:11
by: Nicodem |
Solubility of NBS and succinimide in diethyl ether
Why don't you just measure it up? It is the fastest way to find out since it is very unlikely anybod ... |
17-10-2007 at 09:57
by: Nicodem |
Bromine Source and Synthesis
[quote][i]Originally posted by Antwain[/i]
Can someone tell me why my bromine was so reluctant to l ... |
15-10-2007 at 07:01
by: Nicodem |
Oxidation of THF with nitric acid
TCCA alone only oxidizes THF. The product(s) depends on the presence/absence of water or other proti ... |
14-10-2007 at 00:14
by: Nicodem |
Reduction of Aromatic Nitro compounds with Zn / HCl A write up
Reading this thread, I can not help asking myself why people use messy metal dissolving reductions w ... |
13-10-2007 at 04:00
by: Nicodem |
Reduction of Aromatic Nitro compounds with Zn / HCl A write up
This actual example (o- vs. p-toluidine) does not fit the basic requirements I described above: it d ... |
13-10-2007 at 02:31
by: Nicodem |
Bromine Source and Synthesis
[quote][i]Originally posted by Antwain[/i]
Also, Whilst I was able to come up with the ratio BCDMH ... |
13-10-2007 at 02:03
by: Nicodem |
Reduction of Aromatic Nitro compounds with Zn / HCl A write up
The compounds that can efficiently H-bond with water deviate a lot from the steam distillation laws. ... |
13-10-2007 at 00:55
by: Nicodem |
iodation of double bond benzalacetone
There are no carbocations or tautomers involved (except for the tautomerisation in the last step). I ... |
13-10-2007 at 00:29
by: Nicodem |
3 dimethylamino indole ?
Glycolic acid is used in the Org. Synth. method and not acetic acid.
Forgotten, your posts and qu ... |
12-10-2007 at 00:10
by: Nicodem |
instrumental methods of analysis
What you need for a proper characterization of a new organic compound is at least 1H & 13C NMR, ... |
11-10-2007 at 23:45
by: Nicodem |
iodation of double bond benzalacetone
Filemon: That double bond is too electrophilic to getting iodinated to a stable product. Only very n ... |
11-10-2007 at 23:34
by: Nicodem |
SnCl4:5H2O to SnCl4
Heating over HCl atmosphere is a bit impossible given the volatility of SnCl4.
I guess the simplest ... |
8-10-2007 at 23:29
by: Nicodem |
Bromine Source and Synthesis
Antwain, I'm sorry to hear about the disaster and wish you had no permanent lung damage or other con ... |
7-10-2007 at 12:22
by: Nicodem |
Bromine Source and Synthesis
If you didn't understood then say so. I will gladly explain if I can. But accusing me of sarcasm jus ... |
6-10-2007 at 11:52
by: Nicodem |
Bromine Source and Synthesis
Sarcasm? WTF? Where? 
I answered your questions and even told you where you can find more deta ... |
6-10-2007 at 11:03
by: Nicodem |
Bromine Source and Synthesis
But why? It simply does not make any sense when you can simply reduce BCDMH directly to Br2 and chlo ... |
6-10-2007 at 10:45
by: Nicodem |
Bromine Source and Synthesis
[quote][i]Originally posted by Antwain[/i]
Interesting thread. I have 1kg of bromochlorodimethlyhyd ... |
6-10-2007 at 10:16
by: Nicodem |
Frozen Glass joint?
Besides heating, beating with a wooden hammer and WD40, another thing that sometimes help is to drip ... |
6-10-2007 at 02:12
by: Nicodem |
carboxylic acid functional group
Is that supposed to be a retrosynthetic arrow or a reaction arrow? It does not fit the standards for ... |
3-10-2007 at 11:13
by: Nicodem |
Drying solvents with Al.
It mostly depends on how effective it is in drying THF or other inert solvents. I doubt it can appro ... |
2-10-2007 at 13:50
by: Nicodem |
Reduction Al-Hg
In that case it is isopropanol that is the reducent, not the aluminium ions. The isopropoxide groups ... |
2-10-2007 at 13:35
by: Nicodem |
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