From Organic Chemistry Wiki Spring 2019
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| == Nitrobenzene (Lila Cardozo) ==
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| A reaction of benzene with nitric acid to form nitrobenzene.
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| [[File:Wiki1 nitro.png|1100px]]
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| == By treating tertiary amines with alkaline KMnO4 this gives tertiary nitro compounds. Only with tertiary amines. Alfredo Villalobos-Perez ==
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| [[File:Formation of Nitromethane.png|1100px]]
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| == Reduction of Nitrobenzene by HCl, Sn Brian Sands ==
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| [[File:Nitrobenzene-reduction.png]][http://organicchem.sites.grinnell.edu/wiki/spring19/images/9/98/Nitrobenzene-reduction.png]
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| == Nitration of Pyrrole: Sophie Banegas ==
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| [[File:Nitration of Pyrrole.png]]
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| == Nitration of Indole - Emma Olson ==
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| [[File:Indole_Nitration.jpg|900px]]
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Revision as of 18:31, 19 January 2018