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Help separating HCl from n-butanol
Add excess base cautiously (NaOH, CaO, or so on) and frac dist?
Unlike HCl they arent volatile thus ... |
28-12-2014 at 00:21
by: Pomzazed |
Nomenclature - group abbreviations
These shorthand name are quite widely accepted. They are commonly used "formula" even in the publica ... |
13-7-2014 at 06:13
by: Pomzazed |
Why is there no such compound as H3NO4 ?
d-orbital absent? |
22-3-2014 at 02:53
by: Pomzazed |
Cool product from aldol condensation of acetone
eh? can I bump this?
Althought its 2012 now I still find this interesting, as I could not produce t ... |
23-7-2012 at 20:57
by: Pomzazed |
Making KOH from wood ashes why is it yellow ?
And those mentioned polyaromatics are [b]in[/b]soluble in water, so I doubt this would be the case.
... |
11-9-2010 at 00:24
by: Pomzazed |
Propyl-Iodide Preparation?
[quote]
Also, keep in mind that the potential presence of isomeric alkyl halides in the nucleophili ... |
2-5-2010 at 11:47
by: Pomzazed |
chloric acid solution becomes yellow ...produces a peculiar noise
"produces a peculiar noise"
still wonder what this is xD |
29-4-2010 at 11:02
by: Pomzazed |
Propyl-Iodide Preparation?
[b]@Nicodem[/b]
Yes I know that. But that's why i said i "doubt" he will get [i]"pure"[/i] 1-halopr ... |
29-4-2010 at 10:01
by: Pomzazed |
Acetic Acid substitution in Al/Hg red.
"substrate" went red?
can you specify the reaction you were doing? There are too many reactant that ... |
29-4-2010 at 09:53
by: Pomzazed |
hOW TO PRODUCE HBr INSITU???
KBr + Acid |
28-4-2010 at 17:43
by: Pomzazed |
Propyl-Iodide Preparation?
I doubt you'll get pure 1-halopropane.
acid attacks the alcohol, resulting in a primary carbocation ... |
28-4-2010 at 17:26
by: Pomzazed |
Column chromatography materials
I tend to use the cat-pee sand of the cheapest price bought from the supermarket. It works like sili ... |
19-4-2010 at 02:35
by: Pomzazed |
Camphor: Any interesting experiment?
Aw, wouldn't camphorsultam require reductive amination, sulfonation, and condensation in some order? ... |
16-4-2010 at 11:01
by: Pomzazed |
Camphor: Any interesting experiment?
Beside of sulfonating it to camphorsulfonic acid (and use it as organic acid), or oxidize it to its ... |
14-4-2010 at 02:15
by: Pomzazed |
Determining the configuration at a stereocenter
[IMG]http://i40.photobucket.com/albums/e210/pomzazed/temp-5.jpg[/IMG] |
11-4-2010 at 19:43
by: Pomzazed |
Regioselective sulfonation of Naphthalene?
Wah, thanks [i]UnintentionalChaos[/i]. Don't know how I skipped this topic in the search result, my ... |
8-4-2010 at 23:14
by: Pomzazed |
Regioselective sulfonation of Naphthalene?
Here I got bunchs of >97% Naphthalene in the form of commercial mothballs, and 18M of sulfuric ac ... |
8-4-2010 at 22:09
by: Pomzazed |
Chemical equations in MS Word
Magpie, just drag at the corner in MSWord to reduce the size instead,
Also, applying the ACS styl ... |
11-12-2009 at 20:54
by: Pomzazed |
SnI4: A nice covalent compound of tin
Ah, my bad forgetting the 18 e- things, thanks for refreshing my memory UnintentionalChaos  |
24-9-2009 at 23:25
by: Pomzazed |
SnI4: A nice covalent compound of tin
[rquote=162499&tid=12826&author=Jor]
I'm not sure but if using such a large excess of tin, ... |
24-9-2009 at 19:51
by: Pomzazed |
Straight to base extractions
Arrhenius;
Thanks for posting that. It was basically what I tried to say but at the time i posted ... |
24-5-2009 at 22:22
by: Pomzazed |
Straight to base extractions
This might be possible if the alkaloids is in the form of salt in the plant itself, forming ammonium ... |
22-5-2009 at 17:35
by: Pomzazed |
converting 85-90% KOH to anhydrous KOH?
panziandi, even so, the silver contamination is bad for many reactions! On organic synthesis silver ... |
20-5-2009 at 05:28
by: Pomzazed |
converting 85-90% KOH to anhydrous KOH?
I think there will be alteration at the silver surface, and after then, the inner mass too.
This mi ... |
19-5-2009 at 21:00
by: Pomzazed |
'splain something to me about matter
"Density" ? |
28-4-2009 at 13:02
by: Pomzazed |
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