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	<id>http://organicchem.sites.grinnell.edu/wiki/spring19/api.php?action=feedcontributions&amp;feedformat=atom&amp;user=Sandsbri</id>
	<title>Organic Chemistry Wiki Spring 2019 - User contributions [en]</title>
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	<updated>2026-11-06T06:36:34Z</updated>
	<subtitle>User contributions</subtitle>
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	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Nitro_compound&amp;diff=721</id>
		<title>Talk:Nitro compound</title>
		<link rel="alternate" type="text/html" href="http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Nitro_compound&amp;diff=721"/>
		<updated>2017-02-20T02:16:42Z</updated>

		<summary type="html">&lt;p&gt;Sandsbri: /* Reduction of Nitrobenzene by HCl, Sn Brian Sands */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Main_Page]]&lt;br /&gt;
__TOC__&lt;br /&gt;
&lt;br /&gt;
== Nitrobenzene (Lila Cardozo) ==&lt;br /&gt;
A reaction of benzene with nitric acid to form nitrobenzene.&lt;br /&gt;
[[File:Wiki1 nitro.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== By treating tertiary amines with alkaline KMnO4 this gives tertiary nitro compounds. Only with tertiary amines. Alfredo Villalobos-Perez ==&lt;br /&gt;
&lt;br /&gt;
[[File:Formation of Nitromethane.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Reduction of Nitrobenzene by HCl, Sn Brian Sands ==&lt;br /&gt;
&lt;br /&gt;
[[File:Nitrobenzene-reduction.png]][http://organicchem.sites.grinnell.edu/wiki/spring19/images/9/98/Nitrobenzene-reduction.png]&lt;/div&gt;</summary>
		<author><name>Sandsbri</name></author>
	</entry>
	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Nitro_compound&amp;diff=720</id>
		<title>Talk:Nitro compound</title>
		<link rel="alternate" type="text/html" href="http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Nitro_compound&amp;diff=720"/>
		<updated>2017-02-20T02:16:12Z</updated>

		<summary type="html">&lt;p&gt;Sandsbri: /* Reduction of Nitrobenzene by HCl, Sn */ new section&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Main_Page]]&lt;br /&gt;
__TOC__&lt;br /&gt;
&lt;br /&gt;
== Nitrobenzene (Lila Cardozo) ==&lt;br /&gt;
A reaction of benzene with nitric acid to form nitrobenzene.&lt;br /&gt;
[[File:Wiki1 nitro.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== By treating tertiary amines with alkaline KMnO4 this gives tertiary nitro compounds. Only with tertiary amines. Alfredo Villalobos-Perez ==&lt;br /&gt;
&lt;br /&gt;
[[File:Formation of Nitromethane.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Reduction of Nitrobenzene by HCl, Sn ==&lt;br /&gt;
&lt;br /&gt;
[[File:Nitrobenzene-reduction.png]][http://organicchem.sites.grinnell.edu/wiki/spring19/images/9/98/Nitrobenzene-reduction.png]&lt;/div&gt;</summary>
		<author><name>Sandsbri</name></author>
	</entry>
	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Amine&amp;diff=650</id>
		<title>Talk:Amine</title>
		<link rel="alternate" type="text/html" href="http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Amine&amp;diff=650"/>
		<updated>2017-01-29T22:07:21Z</updated>

		<summary type="html">&lt;p&gt;Sandsbri: /* Brian Sands Week 1 Submission: Simple Amine reacts with Grignard Reagent */ new section&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Main_Page]]&lt;br /&gt;
__TOC__&lt;br /&gt;
&lt;br /&gt;
== Reduction reaction with lithium aluminium hydride gives a phenylmethanamine from a benzonitrile (Rong Guo)==&lt;br /&gt;
&lt;br /&gt;
[[File:Untitled.png|900px]]&lt;br /&gt;
&lt;br /&gt;
== Synthesis of Second-Degree Amine from Aldehyde - Emma Olson ==&lt;br /&gt;
&lt;br /&gt;
[[File:2Amine_Synthesis.png|800px]]&lt;br /&gt;
&lt;br /&gt;
== Brian Sands Week 1 Submission: Simple Amine reacts with Grignard Reagent ==&lt;br /&gt;
&lt;br /&gt;
[http://organicchem.sites.grinnell.edu/wiki/spring19/images/9/9e/Screenshot_%2833%29.png]&lt;/div&gt;</summary>
		<author><name>Sandsbri</name></author>
	</entry>
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