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	<id>http://organicchem.sites.grinnell.edu/wiki/spring19/api.php?action=feedcontributions&amp;feedformat=atom&amp;user=Guorong</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=Guorong"/>
	<link rel="alternate" type="text/html" href="http://organicchem.sites.grinnell.edu/wiki/spring19/Special:Contributions/Guorong"/>
	<updated>2026-11-06T06:36:38Z</updated>
	<subtitle>User contributions</subtitle>
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	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Ether&amp;diff=755</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=755"/>
		<updated>2017-05-08T18:43:15Z</updated>

		<summary type="html">&lt;p&gt;Guorong: /* Claisen Condensation: RongGuo */ 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;br /&gt;
&lt;br /&gt;
== formation of methyl benzoate (Yun Tang) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Wiki2.png|500px]]&lt;br /&gt;
&lt;br /&gt;
== Claisen Condensation: RongGuo ==&lt;br /&gt;
&lt;br /&gt;
[[File:Esterguorong.png|900px]]&lt;/div&gt;</summary>
		<author><name>Guorong</name></author>
	</entry>
	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Ketone&amp;diff=699</id>
		<title>Talk:Ketone</title>
		<link rel="alternate" type="text/html" href="http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Ketone&amp;diff=699"/>
		<updated>2017-02-18T20:04:51Z</updated>

		<summary type="html">&lt;p&gt;Guorong: /* The Clemmensen Reduction  Rong Guo*/&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Main_Page]]&lt;br /&gt;
__TOC__&lt;br /&gt;
&lt;br /&gt;
== Hydrolysis to from Acetone ==&lt;br /&gt;
&lt;br /&gt;
Heather Roesch[[File:Ketone (Acetone).png]]&lt;br /&gt;
&lt;br /&gt;
== Rachel Tappe: Oxidation of an alcohol into a ketone ==&lt;br /&gt;
&lt;br /&gt;
[[File:Screenshot_2017-01-28_15.16.43.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Frieden Crafts Acylation  (Katie McDonald) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Friedel_Crafts_Acylation.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Nucleophilic Addition to Alkyne (Lauren MacKenzie ==&lt;br /&gt;
&lt;br /&gt;
[[File:Rxn_2.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
The product easily transforms between the keto and enol forms (hence the double arrows), but the keto form is predominant.&lt;br /&gt;
&lt;br /&gt;
== Dimethyl ketone by ozonolysis (Kyra Neylan) ==&lt;br /&gt;
&lt;br /&gt;
2,3-dimethylbut-2-ene reacts with ozone and then dimethyl sulfide to form dimethylketone (acetone).&lt;br /&gt;
[[File:Ozonolysis.png|900px]]&lt;br /&gt;
&lt;br /&gt;
== The Clemmensen Reduction Rong Guo==&lt;br /&gt;
&lt;br /&gt;
[[File:The Clemmensen Reduction Rong Guo.png|500px]]&lt;/div&gt;</summary>
		<author><name>Guorong</name></author>
	</entry>
	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Ketone&amp;diff=698</id>
		<title>Talk:Ketone</title>
		<link rel="alternate" type="text/html" href="http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Ketone&amp;diff=698"/>
		<updated>2017-02-18T20:03:48Z</updated>

		<summary type="html">&lt;p&gt;Guorong: /* The Clemmensen Reduction Rong Guo */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Main_Page]]&lt;br /&gt;
__TOC__&lt;br /&gt;
&lt;br /&gt;
== Hydrolysis to from Acetone ==&lt;br /&gt;
&lt;br /&gt;
Heather Roesch[[File:Ketone (Acetone).png]]&lt;br /&gt;
&lt;br /&gt;
== Rachel Tappe: Oxidation of an alcohol into a ketone ==&lt;br /&gt;
&lt;br /&gt;
[[File:Screenshot_2017-01-28_15.16.43.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Frieden Crafts Acylation  (Katie McDonald) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Friedel_Crafts_Acylation.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Nucleophilic Addition to Alkyne (Lauren MacKenzie ==&lt;br /&gt;
&lt;br /&gt;
[[File:Rxn_2.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
The product easily transforms between the keto and enol forms (hence the double arrows), but the keto form is predominant.&lt;br /&gt;
&lt;br /&gt;
== Dimethyl ketone by ozonolysis (Kyra Neylan) ==&lt;br /&gt;
&lt;br /&gt;
2,3-dimethylbut-2-ene reacts with ozone and then dimethyl sulfide to form dimethylketone (acetone).&lt;br /&gt;
[[File:Ozonolysis.png|900px]]&lt;br /&gt;
&lt;br /&gt;
== The Clemmensen Reduction ==&lt;br /&gt;
&lt;br /&gt;
[[File:The Clemmensen Reduction Rong Guo.png|1100px]]&lt;/div&gt;</summary>
		<author><name>Guorong</name></author>
	</entry>
	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Ketone&amp;diff=697</id>
		<title>Talk:Ketone</title>
		<link rel="alternate" type="text/html" href="http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Ketone&amp;diff=697"/>
		<updated>2017-02-18T20:02:05Z</updated>

		<summary type="html">&lt;p&gt;Guorong: /* The Clemmensen Reduction */ new section&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Main_Page]]&lt;br /&gt;
__TOC__&lt;br /&gt;
&lt;br /&gt;
== Hydrolysis to from Acetone ==&lt;br /&gt;
&lt;br /&gt;
Heather Roesch[[File:Ketone (Acetone).png]]&lt;br /&gt;
&lt;br /&gt;
== Rachel Tappe: Oxidation of an alcohol into a ketone ==&lt;br /&gt;
&lt;br /&gt;
[[File:Screenshot_2017-01-28_15.16.43.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Frieden Crafts Acylation  (Katie McDonald) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Friedel_Crafts_Acylation.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Nucleophilic Addition to Alkyne (Lauren MacKenzie ==&lt;br /&gt;
&lt;br /&gt;
[[File:Rxn_2.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
The product easily transforms between the keto and enol forms (hence the double arrows), but the keto form is predominant.&lt;br /&gt;
&lt;br /&gt;
== Dimethyl ketone by ozonolysis (Kyra Neylan) ==&lt;br /&gt;
&lt;br /&gt;
2,3-dimethylbut-2-ene reacts with ozone and then dimethyl sulfide to form dimethylketone (acetone).&lt;br /&gt;
[[File:Ozonolysis.png|900px]]&lt;br /&gt;
&lt;br /&gt;
== The Clemmensen Reduction ==&lt;br /&gt;
&lt;br /&gt;
[[File:Rongguo.png|1100px]]&lt;/div&gt;</summary>
		<author><name>Guorong</name></author>
	</entry>
	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Main_Page&amp;diff=696</id>
		<title>Talk:Main Page</title>
		<link rel="alternate" type="text/html" href="http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Main_Page&amp;diff=696"/>
		<updated>2017-02-18T19:59:28Z</updated>

		<summary type="html">&lt;p&gt;Guorong: /* The Clemmensen Reduction Rong Guo */ new section&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;== The Clemmensen Reduction Rong Guo ==&lt;br /&gt;
&lt;br /&gt;
[[File:The Clemmensen Reduction Rong Guo|1100px]]&lt;/div&gt;</summary>
		<author><name>Guorong</name></author>
	</entry>
	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Amine&amp;diff=635</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=635"/>
		<updated>2017-01-29T18:36:26Z</updated>

		<summary type="html">&lt;p&gt;Guorong: /* Rong Guo: Reduction reaction with lithium aluminium hydride gives a phenylmethanamine from a benzonitrile */&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;/div&gt;</summary>
		<author><name>Guorong</name></author>
	</entry>
	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Amine&amp;diff=634</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=634"/>
		<updated>2017-01-29T18:35:24Z</updated>

		<summary type="html">&lt;p&gt;Guorong: /* Rong Guo: Reduction reaction with lithium aluminium hydride gives a phenylmethanamine from a benzonitrile */ new section&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Main_Page]]&lt;br /&gt;
__TOC__&lt;br /&gt;
&lt;br /&gt;
== Rong Guo: Reduction reaction with lithium aluminium hydride gives a phenylmethanamine from a benzonitrile ==&lt;br /&gt;
&lt;br /&gt;
[[File:Untitled.png|900px]]&lt;/div&gt;</summary>
		<author><name>Guorong</name></author>
	</entry>
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