Ogannessionn
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2,4,6-trinitrotoluene
In doing catalytic reforming of 1,3,5-trinitro heptane, using V2O5/MoO3/Cr2O3 as catalyst at high temperature and pressure,can i get
2,4,6-trinitrotoluene...
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CharlieA
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Do you have any reference for this reaction?
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Ogannessionn
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Nobelium
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fusso
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We want a full link, not a single word.
[Edited on 190101 by fusso]
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WGTR
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This has to be some weird form of spam, or trolling. Carry on.
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maximumrisk
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Seems to be sometimes crazy,
Missing Megas Sites to get Syntheses to some of the TNT-derivates !
(2-CH3, 2,4-CH3 and 2,4,6-CH3)
see: (see not !)
http://roguesci.org/megalomania
More than, some Errors seems to be in the Single Step Syntheses.
What should we do, discussing about theories, or about real working
Explosives.
It could be nice, someone would opening the Database to This !
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j_sum1
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Aaaaaand this one is going nowhere.
I will be generous and relegate it to Beginnings, but if discussion continues with no appreciable content it will end up in Detritus.
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j_sum1
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Thread Moved
16-1-2019 at 17:21 |
XeonTheMGPony
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sounds like a fitting place for this to be.
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Vomaturge
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@maximumrisk, I've been wondering about roguesci too. I have seen it mentioned, and linked to (all broken links, of course) many times in old
sciencemadness threads and not just for drugs/explosives/poisons. The Sciencemadness Wiki has a short article on it, decrying it as supposedly being mainly for the more dangerous/illegal applications of science.
What I know about it now, is that the site owner had a compilation of chemistry data, and also a discussion forum, whose posts have been archived in
two links from the wiki.
Do you know if those links have all the posts from before roguesci went down, or were only some of them archived?
Back on topic: organessionn what makes you think of this reaction? I don't know how 2,4,6 nitrotoluene is made, but I would assume it makes more sense
to start with toluene or benzene and add groups to it then to add all the nitro groups and then try and make it into an aromatic ring without
disturbing them.
Or, is this trolling/ignorance/joking at the lead tri-methane... "goes pop with a decent cap" level.
[Edited on 17-1-2019 by Vomaturge]
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DraconicAcid
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How many words does it take to say "No"?
There's no way you can convert any substituted heptane into toluene under conditions that won't wreck the nitro groups. It's a fantasy from someone
who is just learning chemistry.
Please remember: "Filtrate" is not a verb.
Write up your lab reports the way your instructor wants them, not the way your ex-instructor wants them.
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