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Author: Subject: Urea explorations
guaguanco
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[*] posted on 11-2-2004 at 13:11


Quote:
Originally posted by Friedrich Wöhler
It should be able (I read) to add *CO*-group from urea on carbonyl-building metals such as nickel.


I don't think so. Ni(CO)4 is produced by passing CO gas over powdered Ni, not from solutions of nickel ions. And urea is quite a polar molecule; the carbonyl portion isn't going to easily fly off as a carbon monoxide molecule.
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Friedrich Wöhler
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[*] posted on 11-2-2004 at 14:47


Quote:
not from solutions of nickel ions


Where did you read this...?? I have this not written.

But...I had that could write. Because of its correctly!

Quote:
Ni(CO)4 is produced by passing CO gas over powdered Ni, not from solutions of nickel ions


False!

Generally there are different methods getting carbonyles in addition of that gas - metal-powder - reaction. For example:
~ CO under high pressure on Me-sulfides or Me-chlorides (Hieber-Method) (known carbonyles from minimal 12 metals.)
~ Cr(CO)6 Effect of CO at a etheric solution of CrCl3 under presence of Grignard-compounds
~ [Mn(CO)5]2 CO under pressure at activatet MnI2 in ether, catalysed by Mg
~ Ni(CO)5 already from shaking an alcalic suspension of fresh NiS2 with CO-gas

Get knowledge from chemistry books before contradict so strictly!

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guaguanco
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[*] posted on 11-2-2004 at 15:25


You are correct, I did insufficient homework, you can use nickel ions. :( I still don't think you'll be able to use urea as a carbonyl source. :)
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Polverone
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[*] posted on 11-2-2004 at 15:52


See <A HREF="http://www.sciencemadness.org/talk/viewthread.php?tid=1128">this thread</A>. The use of nickel and urea for producing hydrazine has been patented, but the nickel is supposed to act catalytically, its carbonyl decomposing to again yield metallic nickel and CO.



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guaguanco
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[*] posted on 11-2-2004 at 17:27


Well, my humiliation is well and truly complete.:cool:
My wife still likes me, anyway...
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Friedrich Wöhler
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[*] posted on 12-2-2004 at 11:38


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My wife still likes me, anyway...


I know why: she didn't read this forum. :D:D:D:D:D

Ok ok, don't make suicide, the life will continue! ;)




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Axt
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[*] posted on 1-10-2004 at 19:08


What is the correct term for salts of nitrourea? Ive been using "nitrocarbamate" but now im not entirely sure??
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Theoretic
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[*] posted on 2-10-2004 at 08:56


I'd just say "nitrourate".



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Organikum
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[*] posted on 24-5-2006 at 18:31


Thats a old one but hey!

Polyethlene is a nice reducing agent. isn´t it`?

Melts better into the brew then charcoal.
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[*] posted on 3-2-2008 at 04:23
urea


What real uses has urea , besides a good way of neutralizing NOx vapors?
I used UTFSE , but only came across organic synthesis and preparation of potassium/sodium cyanate (this one needs temperatures around 250C, wich is no options as I only have a spiritus burner (altho I will get a propane/butane one later on))
I do not have a fumehood.


Edit by Chemoleo: You didn't search well enough. Merged with urea exploration thread.

[Edited on 3-2-2008 by chemoleo]
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[*] posted on 3-2-2008 at 04:56


You might start your research here ..........

http://en.wikipedia.org/wiki/Urea

.....then move on with some of the references given to get a deeper view of the compound.

http://webmineral.com/data/Urea.shtml




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YT2095
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[*] posted on 3-2-2008 at 09:22


Quote:
Originally posted by Jor
preparation of potassium/sodium cyanate (this one needs temperatures around 250C, wich is no options as I only have a spiritus burner


your Alcohol burner Should be quite capable of well over 3x this heat (250c). ;)




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[*] posted on 19-7-2016 at 15:08


Quote: Originally posted by Polverone  


I know it's rather silly of me to just start trying things when I could look them up, but I love the hands on parts of chemistry and I was disconnected from the net at the time.



I have the same situation going right now. I don't know what to do with all of this urea.




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