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Hydroxylamine NH2OH Uses (and Production)
Uses of hydroxylamine..... How about converting ketones to amides?
Mix it with a ketone. This for ...
16-3-2005 at 21:21
by: Caffinehog
R-OH to R-leaving group?
I'm familiar with tosylates and mesylates, but has anyone made anything like them at home? And ...
7-3-2005 at 18:24
by: Caffinehog
help:The synthesis of N,N-dimethylformamide di-tert-butyl acetal
Is the product more volatile than the reactants? On the off chance that it is, you could distill it ...
5-3-2005 at 17:48
by: Caffinehog
N-bromo Succinimide
Just remember that this stuff is good for radical reactions, too.
5-3-2005 at 17:47
by: Caffinehog
aniline impurities
Aniline is very easily oxidized, so if you distill it, you're going to get some impurities back ...
5-3-2005 at 17:45
by: Caffinehog
Ethyl ether distillation and synthesis
WOOT! Thanks for the link!
Sodium ethoxide would be best! The carbonate was just an idea to gen ...
3-3-2005 at 23:03
by: Caffinehog
Ethyl ether distillation and synthesis
[quote][i]Originally posted by sparkgap[/i]
That was elaborate, but IIRC, just boiling [b]concentra ...
3-3-2005 at 22:16
by: Caffinehog
Ethyl ether distillation and synthesis
[quote][i]Originally posted by garage chemist[/i]Do you know which reaction happens when a ketone is ...
3-3-2005 at 22:11
by: Caffinehog
Ethyl ether distillation and synthesis
Ethyl ether should be quite easy to make.
Reflux ethanol with sulfuric acid and sodium or potassium ...
3-3-2005 at 21:50
by: Caffinehog
Sciencemadness Discussion Board
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Fundamentals
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» Beginnings
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» Miscellaneous
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» Reagents and Apparatus Acquisition
» Electronics
» Process Engineering
» Materials and Metallurgy
Special Topics
» Analytical Chemistry
» Electrochemistry
» Energetic Materials
» Biochemistry
» Radiochemistry
» Computational Models and Techniques
Literature and Documentation
» Sciencemadness Wiki
» Prepublication
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» Forum Matters
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