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	<id>http://organicchem.sites.grinnell.edu/wiki/spring19/api.php?action=feedcontributions&amp;feedformat=atom&amp;user=Fluharty</id>
	<title>Organic Chemistry Wiki Spring 2019 - User contributions [en]</title>
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	<updated>2026-11-06T06:16:54Z</updated>
	<subtitle>User contributions</subtitle>
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	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Ketone&amp;diff=801</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=801"/>
		<updated>2017-05-09T23:47:04Z</updated>

		<summary type="html">&lt;p&gt;Fluharty: /* Swern Oxidation of Primary Alcohol (Noah Fluharty) */ 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 Rong Guo==&lt;br /&gt;
&lt;br /&gt;
[[File:The Clemmensen Reduction Rong Guo.png|500px]]&lt;br /&gt;
&lt;br /&gt;
== Acetal Formation (Ky-Sean Johnson) ==&lt;br /&gt;
&lt;br /&gt;
[[File:AcetalJohnson.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Heterocycle ketone addition (Lila Cardozo) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Wiki4_heterocycles.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Michael Condensation (Liangchen Liu) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Wiki4.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Swern Oxidation of Primary Alcohol (Noah Fluharty) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Reaction_4.png|1100px]]&lt;/div&gt;</summary>
		<author><name>Fluharty</name></author>
	</entry>
	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Alcohol&amp;diff=726</id>
		<title>Talk:Alcohol</title>
		<link rel="alternate" type="text/html" href="http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Alcohol&amp;diff=726"/>
		<updated>2017-02-20T03:11:21Z</updated>

		<summary type="html">&lt;p&gt;Fluharty: /* HG(OAc)2 Alcohol */ new section&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Main_Page]]&lt;br /&gt;
__TOC__&lt;br /&gt;
&lt;br /&gt;
[[File:Tert-Butyl Alcohol.png|100px.]]&lt;br /&gt;
&lt;br /&gt;
== DeRoche Grignard Reaction ==&lt;br /&gt;
&lt;br /&gt;
[[File:Grignard_Reaction.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Ethanol (Beth Ann Hansen) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Ester_to_Alcohol_with_LiAlH4.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Butanol Ky-Sean Johnson ==&lt;br /&gt;
&lt;br /&gt;
[[File:AlcoholJohnson.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Primary alcohol from acid chloride (Katie McDonald) ==&lt;br /&gt;
&lt;br /&gt;
[[File:OchemWiki1.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Formation of cyclopentane-1,2-diol (Hannah Hong) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Alcohol_formation.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Hydroboration reaction (Lila Cardozo) ==&lt;br /&gt;
&lt;br /&gt;
Hyrdoboration reaction of 1-methylcyclopent-1-ene to produce 2-methylcyclopentan-1-ol&lt;br /&gt;
[[File:Wiki2_alcohol.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Ozonolysis (Xiaobo Sun) ==&lt;br /&gt;
&lt;br /&gt;
[[File: Untitled_Document-1.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== HG(OAc)2 Alcohol ==&lt;br /&gt;
&lt;br /&gt;
[[File:Screen_Shot_2017-02-19_at_9.01.41_PM.png|1100px]]&lt;/div&gt;</summary>
		<author><name>Fluharty</name></author>
	</entry>
	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Carboxylic_Acid&amp;diff=623</id>
		<title>Talk:Carboxylic Acid</title>
		<link rel="alternate" type="text/html" href="http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Carboxylic_Acid&amp;diff=623"/>
		<updated>2017-01-27T01:46:42Z</updated>

		<summary type="html">&lt;p&gt;Fluharty: /* Chromium Trioxide to Carboxylic Acid (Noah Fluharty) */ new section&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Main_Page]]&lt;br /&gt;
__TOC__&lt;br /&gt;
&lt;br /&gt;
== CO2 to Carboxylic Acid (Lauren MacKenzie ==&lt;br /&gt;
&lt;br /&gt;
In this reaction, an organometallic reagent reacts with CO2 (in a solution of diethyl ether) to create an intermediate, which reacts with H3O+ to create a carboxylic acid. &lt;br /&gt;
&lt;br /&gt;
[[File: CO2_to_Carboxylic_Acid.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Cyanonitrile to Carboxylic Acid (Kyra Neylan) ==&lt;br /&gt;
Reaction of propanonitrile in water with acid and heat to form propanoic acid and ammonium.&lt;br /&gt;
[[File: Cyanonitrile_to_Carboxylic_Acid_(Kyra_Neylan).png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Chromium Trioxide to Carboxylic Acid (Noah Fluharty) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Chem_Wiki_1.png|1100px]]&lt;/div&gt;</summary>
		<author><name>Fluharty</name></author>
	</entry>
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