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	<id>http://organicchem.sites.grinnell.edu/wiki/spring19/api.php?action=feedcontributions&amp;feedformat=atom&amp;user=Schreine</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=Schreine"/>
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	<updated>2026-11-06T04:14:52Z</updated>
	<subtitle>User contributions</subtitle>
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	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Alkane&amp;diff=1080</id>
		<title>Talk:Alkane</title>
		<link rel="alternate" type="text/html" href="http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Alkane&amp;diff=1080"/>
		<updated>2018-05-07T19:55:24Z</updated>

		<summary type="html">&lt;p&gt;Schreine: /* Quiz Problem from 4/2 (Gretchen Schreiner) */ new section&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Main_Page]]&lt;br /&gt;
__TOC__&lt;br /&gt;
&lt;br /&gt;
== Butane (Prof. Swartz) ==&lt;br /&gt;
A reaction of butyl bromide with lithium and then ethanol to form butane.&lt;br /&gt;
&lt;br /&gt;
[[File:Alkane_synthesis.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Ethane (Madison Wardlaw) ==&lt;br /&gt;
&lt;br /&gt;
The hydrogenation of ethene using a nickel catalyst to form ethane. [[File:WIKI_Assignment_2_PNG.png]]&lt;br /&gt;
&lt;br /&gt;
== Quiz Problem from 4/2 (Gretchen Schreiner) ==&lt;br /&gt;
&lt;br /&gt;
1-(cyclohex-3-en-1-yl)ethan-1-one is first deprotonated by LDA and then reacts with propyl bromide via Sn2 to produce a new C-C bond with bromide ion as a leaving group. [[File:Chem_222_Wiki_4_Sn2_C-C_bond_made.png|800px]]&lt;/div&gt;</summary>
		<author><name>Schreine</name></author>
	</entry>
	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Carboxylic_Acid&amp;diff=1078</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=1078"/>
		<updated>2018-05-07T19:37:44Z</updated>

		<summary type="html">&lt;p&gt;Schreine: /* Decarboxylation Reaction (Gretchen Schreiner) */ new section&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|800px]]&lt;br /&gt;
&lt;br /&gt;
== Pentanoic Acid (Xinming Li) ==&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
A Grignard reagent reacts with carbon dioxide and acid to form a carboxylic acid[[File:Untitledzwei.png|1000px|600px]]&lt;br /&gt;
&lt;br /&gt;
== Butanoic Acid (Caleb Lee) ==&lt;br /&gt;
&lt;br /&gt;
Formation of Butanoic Acid via hydrolysis of nitrile &lt;br /&gt;
&lt;br /&gt;
[[File:Preparation_of_Butanoic_Acid.png|1000px]]&lt;br /&gt;
&lt;br /&gt;
== Propanoic Acid (James Mersch) ==&lt;br /&gt;
&lt;br /&gt;
[[File:(James Mersch) Carboxylic acid1.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Base Promoted Halogenation (Matthew Record) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Base_promoted_halogenation.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Benzoic Acid (Xinming Li) 2 ==&lt;br /&gt;
&lt;br /&gt;
[[File:Untitleddrei.png|800px]]&lt;br /&gt;
&lt;br /&gt;
== Aldehyde (Gabi Gryc) ==&lt;br /&gt;
&lt;br /&gt;
Formation of carboxylic acid from an aldehyde&lt;br /&gt;
&lt;br /&gt;
[[File:Carboxylic_acid_wiki_assignment_2.png|1000px]]&lt;br /&gt;
&lt;br /&gt;
== Breaking of ring by ester to carboxylic acid reaction (Benjamin Lim) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Untitled_Document-1_copy.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Heteroauxin Formation (Christine Solomon) ==&lt;br /&gt;
&lt;br /&gt;
[[File:WIkiRxnCarboxylicAcid.png|800px]]&lt;br /&gt;
&lt;br /&gt;
== Decarboxylation Reaction (Gretchen Schreiner) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Chem_222_Wiki_3_Decarboxylation.png|800px]]&lt;/div&gt;</summary>
		<author><name>Schreine</name></author>
	</entry>
	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Ketone&amp;diff=995</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=995"/>
		<updated>2018-02-03T02:34:16Z</updated>

		<summary type="html">&lt;p&gt;Schreine: /* Converting an Ester to Ketone (Gretchen Schreiner) */ new section&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;/div&gt;</summary>
		<author><name>Schreine</name></author>
	</entry>
	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Carboxylic_Acid&amp;diff=911</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=911"/>
		<updated>2018-01-23T03:07:27Z</updated>

		<summary type="html">&lt;p&gt;Schreine: /* 3-chlorobenzoic acid (Gretchen Schreiner) */ new section&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;/div&gt;</summary>
		<author><name>Schreine</name></author>
	</entry>
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