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	<id>http://organicchem.sites.grinnell.edu/wiki/spring19/api.php?action=feedcontributions&amp;feedformat=atom&amp;user=Inturira</id>
	<title>Organic Chemistry Wiki Spring 2019 - User contributions [en]</title>
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	<updated>2026-11-06T06:26:09Z</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=1032</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=1032"/>
		<updated>2018-02-07T01:52:55Z</updated>

		<summary type="html">&lt;p&gt;Inturira: /* Butan-2-one (conversion of nitrile to ketone) (Raghu Inturi) */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Main_Page]]&lt;br /&gt;
__TOC__&lt;br /&gt;
&lt;br /&gt;
== Acetophenone (Kelsey Zhang) ==&lt;br /&gt;
&lt;br /&gt;
[[File: Oxidation_of_alcohol_to_ketone_by_oxidant_Cr.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
oxidation of alcohol to ketone by oxidant Cr&lt;br /&gt;
&lt;br /&gt;
== Converting an Ester to Ketone (Gretchen Schreiner) ==&lt;br /&gt;
&lt;br /&gt;
The ester in ethyl 4-methoxybenzoate is converted to a ketone via protonation, conversion into an acyl chloride, and nucleophilic attack by EtMgBr.[[File:Chem_222_Wiki_2_Ketone_Gretchen_Schreiner.png|800px]]&lt;br /&gt;
&lt;br /&gt;
== butan-2-one (Maverick Zhang) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Ketone.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
But-1-yne reacts with water and sulfuric acid to form butan-2-one.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
----&lt;br /&gt;
&lt;br /&gt;
== Butan-2-one (conversion of nitrile to ketone) (Raghu Inturi) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Grignard_Ketone_synthesis.png]]&lt;br /&gt;
&lt;br /&gt;
Using a Grignard Reagent such as MgBr and water, acetonitrile is converted to butan-2-one.&lt;/div&gt;</summary>
		<author><name>Inturira</name></author>
	</entry>
	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Ketone&amp;diff=1031</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=1031"/>
		<updated>2018-02-07T01:52:17Z</updated>

		<summary type="html">&lt;p&gt;Inturira: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Main_Page]]&lt;br /&gt;
__TOC__&lt;br /&gt;
&lt;br /&gt;
== Acetophenone (Kelsey Zhang) ==&lt;br /&gt;
&lt;br /&gt;
[[File: Oxidation_of_alcohol_to_ketone_by_oxidant_Cr.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
oxidation of alcohol to ketone by oxidant Cr&lt;br /&gt;
&lt;br /&gt;
== Converting an Ester to Ketone (Gretchen Schreiner) ==&lt;br /&gt;
&lt;br /&gt;
The ester in ethyl 4-methoxybenzoate is converted to a ketone via protonation, conversion into an acyl chloride, and nucleophilic attack by EtMgBr.[[File:Chem_222_Wiki_2_Ketone_Gretchen_Schreiner.png|800px]]&lt;br /&gt;
&lt;br /&gt;
== butan-2-one (Maverick Zhang) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Ketone.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
But-1-yne reacts with water and sulfuric acid to form butan-2-one.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
----&lt;br /&gt;
&lt;br /&gt;
== Butan-2-one (conversion of nitrile to ketone) (Raghu Inturi) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Grignard_Ketone_synthesis.png]]&lt;br /&gt;
&lt;br /&gt;
Using a Grignard Reagent such as MgBr, acetonitrile is converted to butan-2-one.&lt;/div&gt;</summary>
		<author><name>Inturira</name></author>
	</entry>
	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Carboxylic_Acid&amp;diff=931</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=931"/>
		<updated>2018-01-23T16:54:31Z</updated>

		<summary type="html">&lt;p&gt;Inturira: /* 3-chlorobenzoic acid (Gretchen Schreiner) */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Main_Page]]&lt;br /&gt;
__TOC__&lt;br /&gt;
&lt;br /&gt;
== 3-chlorobenzoic acid (Gretchen Schreiner) ==&lt;br /&gt;
&lt;br /&gt;
A reaction of 1-bromo-3-chlorobenzene with butyl lithium, then carbon dioxide, and then protonated to form 3-chlorobenzoic acid.&lt;br /&gt;
[[File:Chem_222_Wiki_1_Carboxylic_Acid_Gretchen.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
----&lt;br /&gt;
&lt;br /&gt;
== Acetic Acid (Raghu Inturi) ==&lt;br /&gt;
&lt;br /&gt;
Acetyl Chloride reacts with water to produce Acetic Acid&lt;br /&gt;
&lt;br /&gt;
[[File:Acetic Acid.png|1100px]]&lt;/div&gt;</summary>
		<author><name>Inturira</name></author>
	</entry>
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