Talk:Nitro compound: Difference between revisions

From Organic Chemistry Wiki Spring 2018
Jump to navigation Jump to search
← Older edit
Parkgrac (talk | contribs)
7 edits
 
(8 intermediate revisions by 6 users not shown)
Line 2: Line 2:
__TOC__
__TOC__


== Nitrobenzene (Lila Cardozo) ==
== Nitration of Benzene through aromatic substitution. Jacob Byerly-Duke ==
A reaction of benzene with nitric acid to form nitrobenzene.
[[File:Wiki1 nitro.png|1100px]]


== By treating tertiary amines with alkaline KMnO4 this gives tertiary nitro compounds. Only with tertiary amines. Alfredo Villalobos-Perez ==
[[File:Byerlydu_benzene_nitration.png|700px]]


[[File:Formation of Nitromethane.png|1100px]]
== Nitration of Furan (Madison Wardlaw) ==


== Reduction of Nitrobenzene by HCl, Sn ==
[[File:Wiki_assignment_3.png|850px]]
Nitration of furan through electrophilic substitution mechanism and acid catalyst


[[File:Nitrobenzene-reduction.png]][http://organicchem.sites.grinnell.edu/s18/wiki/images/9/98/Nitrobenzene-reduction.png]
== Quinoline Reaction (Grace Park) ==
 
[[File:Untitled.png]]

Latest revision as of 13:54, 11 May 2018

Main_Page

Nitration of Benzene through aromatic substitution. Jacob Byerly-Duke

Nitration of Furan (Madison Wardlaw)

Nitration of furan through electrophilic substitution mechanism and acid catalyst

Quinoline Reaction (Grace Park)

Retrieved from "http://organicchem.sites.grinnell.edu/s18/wiki/index.php?title=Talk:Nitro_compound&oldid=1147"