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	<id>http://organicchem.sites.grinnell.edu/wiki/spring19/api.php?action=feedcontributions&amp;feedformat=atom&amp;user=Jennings</id>
	<title>Organic Chemistry Wiki Spring 2019 - User contributions [en]</title>
	<link rel="self" type="application/atom+xml" href="http://organicchem.sites.grinnell.edu/wiki/spring19/api.php?action=feedcontributions&amp;feedformat=atom&amp;user=Jennings"/>
	<link rel="alternate" type="text/html" href="http://organicchem.sites.grinnell.edu/wiki/spring19/Special:Contributions/Jennings"/>
	<updated>2026-11-06T06:16:31Z</updated>
	<subtitle>User contributions</subtitle>
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	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Nitrile&amp;diff=853</id>
		<title>Talk:Nitrile</title>
		<link rel="alternate" type="text/html" href="http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Nitrile&amp;diff=853"/>
		<updated>2017-05-12T19:09:50Z</updated>

		<summary type="html">&lt;p&gt;Jennings: /* Jennings_4th pass_Synthesis of 2-(1H-indol-3-yl)acetonitrile via NaCN and 3-(chloromethyl)-1H-indole */ new section&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Main_Page]]&lt;br /&gt;
__TOC__&lt;br /&gt;
&lt;br /&gt;
== Nitrile (Hannah Hong) ==&lt;br /&gt;
&lt;br /&gt;
A reaction of an amide with thionyl chloride to form a nitrile.&lt;br /&gt;
&lt;br /&gt;
[[File:Nitrile.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Hydrolysis of Nitrile ==&lt;br /&gt;
&lt;br /&gt;
A process of Nitrile hydrolysis (Two H2O attacks) that generates carboxylic acid with no change to the carbon chain.&lt;br /&gt;
[[File:Hydrolysis_of_nitrile.png]]&lt;br /&gt;
&lt;br /&gt;
== Creating a Nitrile using an amide and phosphorus(V) oxide (Guzman, Iridian) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Making Nitriles from amides.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Jennings_4th pass_Synthesis of 2-(1H-indol-3-yl)acetonitrile via NaCN and 3-(chloromethyl)-1H-indole ==&lt;br /&gt;
&lt;br /&gt;
[[File:Acetonitrile.png]]&lt;/div&gt;</summary>
		<author><name>Jennings</name></author>
	</entry>
	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Amine&amp;diff=851</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=851"/>
		<updated>2017-05-12T18:55:45Z</updated>

		<summary type="html">&lt;p&gt;Jennings: /* Synthesis of 2-aminobutanoic acid_jennings */&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;br /&gt;
&lt;br /&gt;
== Formation of aniline with nitrobenzene and tetrahydrothiophene 1,1-dioxide :Jason Jennings  ==&lt;br /&gt;
&lt;br /&gt;
[[File:Amine.png]]&lt;br /&gt;
&lt;br /&gt;
== Reduction with an amide (Hannah Hong) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Wiki_3.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Synthesis of 2-aminobutanoic acid_jennings_3rd pass ==&lt;br /&gt;
&lt;br /&gt;
[[File:Aminobutanoic_acid.png]]&lt;/div&gt;</summary>
		<author><name>Jennings</name></author>
	</entry>
	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Amine&amp;diff=850</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=850"/>
		<updated>2017-05-12T18:55:28Z</updated>

		<summary type="html">&lt;p&gt;Jennings: /* Synthesis of 2-aminobutanoic acid_jennings */&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;br /&gt;
&lt;br /&gt;
== Formation of aniline with nitrobenzene and tetrahydrothiophene 1,1-dioxide :Jason Jennings  ==&lt;br /&gt;
&lt;br /&gt;
[[File:Amine.png]]&lt;br /&gt;
&lt;br /&gt;
== Reduction with an amide (Hannah Hong) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Wiki_3.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Synthesis of 2-aminobutanoic acid_jennings ==&lt;br /&gt;
&lt;br /&gt;
[[File:Aminobutanoic_acid.png]]&lt;br /&gt;
3rd pass&lt;/div&gt;</summary>
		<author><name>Jennings</name></author>
	</entry>
	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Amine&amp;diff=849</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=849"/>
		<updated>2017-05-12T18:55:15Z</updated>

		<summary type="html">&lt;p&gt;Jennings: /* Synthesis of 2-aminobutanoic acid_jennings */&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;br /&gt;
&lt;br /&gt;
== Formation of aniline with nitrobenzene and tetrahydrothiophene 1,1-dioxide :Jason Jennings  ==&lt;br /&gt;
&lt;br /&gt;
[[File:Amine.png]]&lt;br /&gt;
&lt;br /&gt;
== Reduction with an amide (Hannah Hong) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Wiki_3.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Synthesis of 2-aminobutanoic acid_jennings ==&lt;br /&gt;
&lt;br /&gt;
[[File:Aminobutanoic_acid.png]]&lt;/div&gt;</summary>
		<author><name>Jennings</name></author>
	</entry>
	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Amine&amp;diff=848</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=848"/>
		<updated>2017-05-12T18:53:59Z</updated>

		<summary type="html">&lt;p&gt;Jennings: /* Synthesis of 2-aminobutanoic acid_jennings */&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;br /&gt;
&lt;br /&gt;
== Formation of aniline with nitrobenzene and tetrahydrothiophene 1,1-dioxide :Jason Jennings  ==&lt;br /&gt;
&lt;br /&gt;
[[File:Amine.png]]&lt;br /&gt;
&lt;br /&gt;
== Reduction with an amide (Hannah Hong) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Wiki_3.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Synthesis of 2-aminobutanoic acid_jennings ==&lt;br /&gt;
&lt;br /&gt;
[[File:Aminobutanoic acid.png&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Jump to: navigation, search ]]&lt;/div&gt;</summary>
		<author><name>Jennings</name></author>
	</entry>
	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Amine&amp;diff=847</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=847"/>
		<updated>2017-05-12T18:51:03Z</updated>

		<summary type="html">&lt;p&gt;Jennings: /* Synthesis of 2-aminobutanoic acid_jennings */ 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;br /&gt;
&lt;br /&gt;
== Formation of aniline with nitrobenzene and tetrahydrothiophene 1,1-dioxide :Jason Jennings  ==&lt;br /&gt;
&lt;br /&gt;
[[File:Amine.png]]&lt;br /&gt;
&lt;br /&gt;
== Reduction with an amide (Hannah Hong) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Wiki_3.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Synthesis of 2-aminobutanoic acid_jennings ==&lt;br /&gt;
&lt;br /&gt;
[http://organicchem.sites.grinnell.edu/wiki/spring19/File:Aminobutanoic_acid.png]&lt;/div&gt;</summary>
		<author><name>Jennings</name></author>
	</entry>
	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Amine&amp;diff=728</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=728"/>
		<updated>2017-02-20T04:30:48Z</updated>

		<summary type="html">&lt;p&gt;Jennings: /* Formation of aniline with nitrobenzene and tetrahydrothiophene 1,1-dioxide :Jason Jennings  */ 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;br /&gt;
&lt;br /&gt;
== Formation of aniline with nitrobenzene and tetrahydrothiophene 1,1-dioxide :Jason Jennings  ==&lt;br /&gt;
&lt;br /&gt;
[[File:Amine.png]]&lt;/div&gt;</summary>
		<author><name>Jennings</name></author>
	</entry>
	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Ether&amp;diff=639</id>
		<title>Talk:Ether</title>
		<link rel="alternate" type="text/html" href="http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Ether&amp;diff=639"/>
		<updated>2017-01-29T20:38:19Z</updated>

		<summary type="html">&lt;p&gt;Jennings: /* Formation of Enol Ether via Acid Catalyst of Acetal_jennings */ new section&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Main_Page]]&lt;br /&gt;
__TOC__&lt;br /&gt;
&lt;br /&gt;
== Williamson Ether Synthesis (Ian Windham) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Ether_Example.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Formation of Enol Ether via Acid Catalyst of Acetal_jennings ==&lt;br /&gt;
&lt;br /&gt;
[[File:Formation of Enol Ether.png]]&lt;/div&gt;</summary>
		<author><name>Jennings</name></author>
	</entry>
</feed>