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Mr. Cool (nick's) website
Does anyone have Mr. Cool's (on E&W forum) website. I used to have it.....but i've los ... |
5-6-2003 at 02:23
by: fluffy bunny |
My Cr@Zy Nitrobenzene
thankyou for the suggestion a_bab, i'll try that....
However i had the conception that nitro ... |
5-6-2003 at 02:19
by: fluffy bunny |
My Cr@Zy Nitrobenzene
I have left my lab unnatended for a couple of months, and some nitrobenzene which was being stored t ... |
1-6-2003 at 20:45
by: fluffy bunny |
substance that creates heat
If its a solid material you are after which will produce considerable heat when dissolved/added to w ... |
5-5-2003 at 00:50
by: fluffy bunny |
DNPA
Sorry this post isn't very helpful, i don't know anything about the synthesis of DNPA, but ... |
22-4-2003 at 18:11
by: fluffy bunny |
trinitroresorcimol from picric acid
I thought that dichlorobenzene was impossible to nitrate because of the highly deactivating afect of ... |
12-4-2003 at 00:11
by: fluffy bunny |
Resorcinol synthesis
I'm trying to find a method for synthesising resorcinol, for producing styphnic acid (trinitror ... |
9-3-2003 at 19:41
by: fluffy bunny |
reduction of syphnic acid
Yes that is certainly possible! Theoretically, any aromatic-amine can be diazotised.
However, there ... |
1-3-2003 at 01:34
by: fluffy bunny |
Aniline
A_bab, if you could please post that synthesis of aniline whenever you get a chance, i would really ... |
24-2-2003 at 23:24
by: fluffy bunny |
Gringard' Regent
The Grignard reagent, is an organometallic reagent where magnesium is inserted between an alkyl grou ... |
22-2-2003 at 15:48
by: fluffy bunny |
Aniline
thanks for your help madscientist, and everyone else, and i'd really appreciate it if you wrote ... |
20-2-2003 at 21:29
by: fluffy bunny |
Aniline
Great thats really helpful, thanks.
But does anyone have an actual detailed synthesis with quantiti ... |
18-2-2003 at 12:40
by: fluffy bunny |
Aniline
I have recently synthesized about 25g of nitrobenzene and wish to form aniline by reduction, and the ... |
18-2-2003 at 02:59
by: fluffy bunny |
Aromatic substitution reactions
Damn the diagram didn't work. Oh well as long as you can understand the question. |
27-1-2003 at 16:47
by: fluffy bunny |
One more question?
Ok. i have read more about different groups and the aromatic ring and how they affect further substi ... |
27-1-2003 at 16:44
by: fluffy bunny |
Aromatic substitution reactions
Thanks alot for that polverone that was just what i was looking for.
Well, i do have a chemistry bo ... |
25-1-2003 at 15:40
by: fluffy bunny |
Aromatic substitution reactions
I'd just like to know what the variables are that make different aromatic rings harder or easier to ... |
24-1-2003 at 02:13
by: fluffy bunny |
Elemental bromine isolation
Madscientist, you do realise sulphuric acid reacts with KMnO4 to produce manganese septoxide don't y ... |
21-1-2003 at 22:36
by: fluffy bunny |
Phenol
Im confused. Someone sugggested turning, toluene to benzene with AlCl3, via the Friedel-Crafts react ... |
21-1-2003 at 04:45
by: fluffy bunny |
benzaldehyde
Interesting experiments. Is benzaldehyde your ultimate goal from all of these experiments?
If it i ... |
20-1-2003 at 16:10
by: fluffy bunny |
DDNP
Microtek, i don't think its the purity of your chemicals that is failing your DDNP synthesis, well, ... |
11-1-2003 at 00:43
by: fluffy bunny |
Sodium Azide
Nick F, i haven't tried the route for making semicarbazide myself, but another member (who seems to ... |
21-10-2002 at 00:18
by: fluffy bunny |
Sodium Azide
Yes, it can be made by the reaction of hydrazine hydrate with isopropyl/ethyl nitrite ([b]not nitrat ... |
19-10-2002 at 22:12
by: fluffy bunny |
