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Author: Subject: Nitrostyrene-like reduction
lestimao
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[*] posted on 4-10-2012 at 04:13
Nitrostyrene-like reduction


Hello,

to perform a nitrostyrene reduction, I've read that is needed acetic acid. I know the acetic acid is a polar protic solvent, so is that why we need the acid, to dissolve the nitrostyrene? Could anyone please explain me this point? Thanks you all!
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hissingnoise
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[*] posted on 4-10-2012 at 04:25


Obvious cooks looking for info are shown little shrift here!
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lestimao
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[*] posted on 4-10-2012 at 04:29


No idea what do you mean about "obvius cooks", I'm only trying to understand that reduction mechanism.
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hissingnoise
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[*] posted on 4-10-2012 at 06:23


Energetic polymers? Yeah, right!
Like this?

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mr.crow
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[*] posted on 4-10-2012 at 06:56


I don't think its cooking, he wants to understand a reaction that interests him



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lestimao
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[*] posted on 4-10-2012 at 07:43


Quote: Originally posted by hissingnoise  
Energetic polymers? Yeah, right!
Like this?



No, nothing like that. Nothing like erowid-related.

I'm interested in halogenated benzene ring, its polymers and redox reactions of different "strenght" (sorry for the lack of chemical language, amateur chemist here).

So, I want to understand why they mention to use acetic acid, and if its to dissolve the nitrostyrene, should it work with halogenated compounds?
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Ephesian
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[*] posted on 4-10-2012 at 07:55



Quote:

Obvious cooks looking for info are shown little shrift here!


Why is there even a science forum, when every question gets belittled with drug cook acquisitions?

Keep being interested in chemistry lestimao, regardless if your interest lies with making "illegal substances"



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hissingnoise
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[*] posted on 4-10-2012 at 08:22


Quote:
Keep being interested in chemistry lestimao, regardless if your interest lies with making "illegal substances"

That's my attitude too . . .
I'll never be into meth, but 'blues' had me for a while in the early seventies; my staple now is sativa-dominant skunk!

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Nicodem
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4-10-2012 at 09:18
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[*] posted on 4-10-2012 at 09:54


Quote: Originally posted by lestimao  
Hello,

to perform a nitrostyrene reduction, I've read that is needed acetic acid.

If you were able to read that, you might as well read also the forum guidelines and learn that we are not clairvoyant. How could you ever expect a meaningful reply, if you don't even give the reference for the reaction you talk about?




…there is a human touch of the cultist “believer” in every theorist that he must struggle against as being unworthy of the scientist. Some of the greatest men of science have publicly repudiated a theory which earlier they hotly defended. In this lies their scientific temper, not in the scientific defense of the theory. - Weston La Barre (Ghost Dance, 1972)

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ChemistryGhost
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[*] posted on 4-10-2012 at 13:03


Now's my chance before this possibly gets sent to detritus!
It's pronounced Cule (like in cube). Nothing personal. It's more directed toward life and not you. Study up though. Try to not look foolish.



U R K3wl!.png - 132kB

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Edit: I added something


Sci cool.png - 51kB <-- Cool

[Edited on 4-10-2012 by ChemistryGhost]




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SM2
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[*] posted on 4-10-2012 at 13:08


so politically correct, it's just wrong.
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