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	<id>http://organicchem.sites.grinnell.edu/wiki/spring19/api.php?action=feedcontributions&amp;feedformat=atom&amp;user=Kimyease</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=Kimyease"/>
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	<updated>2026-11-06T06:36:40Z</updated>
	<subtitle>User contributions</subtitle>
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	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Alkene&amp;diff=1098</id>
		<title>Talk:Alkene</title>
		<link rel="alternate" type="text/html" href="http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Alkene&amp;diff=1098"/>
		<updated>2018-05-08T03:52:30Z</updated>

		<summary type="html">&lt;p&gt;Kimyease: /* Dehydration of Alcohol (Yeaseul Kim) */ new section&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Main_Page]]&lt;br /&gt;
__TOC__&lt;br /&gt;
&lt;br /&gt;
== Wittig Reaction (Matthew Palmeri) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Wiki Entry 1.png|1000px]]&lt;br /&gt;
&lt;br /&gt;
== Halogenated hydrocarbon elimination (Suze Jiang) ==&lt;br /&gt;
&lt;br /&gt;
[[File:1.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Ketone to Alkene: Formation of N,_N,_1-trimethylethenamine (Yuwei Pan) ==&lt;br /&gt;
&lt;br /&gt;
[[File:N,_N,_1-trimethylethenamine.png|600px]]&lt;br /&gt;
&lt;br /&gt;
== Crossed Aldol (Christine Solomon) ==&lt;br /&gt;
&lt;br /&gt;
[[File:WikiRxnCrossedAldolAlkene.png|800px]]&lt;br /&gt;
&lt;br /&gt;
== Hydrogenation of an Alkyne to an Alkene (Madison Wardlaw) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Wiki_assignment_4.png|825px]]&lt;br /&gt;
Using a hydrogen-palladium catalyst in the presence of quinoline reduces the alkyne to an alkene and forms a cis product.&lt;br /&gt;
&lt;br /&gt;
== Diels-Alder Reaction (Ed Lopatto) ==&lt;br /&gt;
&lt;br /&gt;
[[File:DielsAlder_Wiki_Lopatto.png|500px]]&lt;br /&gt;
&lt;br /&gt;
== Dehydration of Alcohol (Yeaseul Kim) ==&lt;br /&gt;
&lt;br /&gt;
[[File: Dehydration_of_Primary_Alcohol.png|1100px]]&lt;/div&gt;</summary>
		<author><name>Kimyease</name></author>
	</entry>
	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Alkane&amp;diff=1092</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=1092"/>
		<updated>2018-05-08T03:15:43Z</updated>

		<summary type="html">&lt;p&gt;Kimyease: /* Reduction of Butan-2-ol to Butane (Yeaseul Kim) */ 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;br /&gt;
&lt;br /&gt;
== Pentane (Imany Noel) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Pentane.jpeg]]&lt;br /&gt;
&lt;br /&gt;
The reaction of 2-pentene with hydrogen gas and palladium to form pentane.&lt;br /&gt;
&lt;br /&gt;
== Reduction of Butan-2-ol to Butane (Yeaseul Kim) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Reduction_of_Butan-2-ol_to_Butane.png|1100px]]&lt;/div&gt;</summary>
		<author><name>Kimyease</name></author>
	</entry>
	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Alcohol&amp;diff=1064</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=1064"/>
		<updated>2018-02-10T01:26:47Z</updated>

		<summary type="html">&lt;p&gt;Kimyease: /* Diol formation (Yeaseul Kim) */ new section&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Main_Page]]&lt;br /&gt;
__TOC__&lt;br /&gt;
&lt;br /&gt;
== Pentanol (Madison Wardlaw) ==&lt;br /&gt;
&lt;br /&gt;
[[File:WIKI_Rxn_1.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== cyclopentanol (Edward Lopatto) ==&lt;br /&gt;
A reaction of cyclopentanone with lithium aluminum hydride and then hydronium to form cyclopentanol.&lt;br /&gt;
[[File:Making_an_alcohol.png|500px]]&lt;br /&gt;
&lt;br /&gt;
== 2-methylpropan-2-ol (Mikayla Kricfalusi) ==&lt;br /&gt;
&lt;br /&gt;
Reacting an alkane with water and H2SO4 to create an alcohol&lt;br /&gt;
&lt;br /&gt;
[[File:alcohol.png]]&lt;br /&gt;
&lt;br /&gt;
== Cyclohexylmethanol (Sam LaMotte) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Cyclohexylmethanol.png|1000px]]&lt;br /&gt;
&lt;br /&gt;
== 2-methyl-1-phenylpropan-2-ol (Gabi Gryc) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Grignard.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
Tertiary alcohol formation from Grignard Reagent&lt;br /&gt;
&lt;br /&gt;
== 3-ethylpentan-3-ol (Michael Hewitt) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Screen Shot 2018-01-22 at 10.28.19 AM.png]]&lt;br /&gt;
&lt;br /&gt;
== Addition of Hydrides to Esters (Emma Bechler) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Addition_of_Hydrides_to_Esters.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Hydroboration Oxidation (Jacob Morsch) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Alcohol_Reaction.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== 3-methylbutan-2-ol (Grace Park) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Alcoholgp.png|900px]]&lt;br /&gt;
&lt;br /&gt;
== Diol formation (Yeaseul Kim) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Diol_formation.png|1100px]]&lt;/div&gt;</summary>
		<author><name>Kimyease</name></author>
	</entry>
	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Alkyl_Halide&amp;diff=967</id>
		<title>Talk:Alkyl Halide</title>
		<link rel="alternate" type="text/html" href="http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Alkyl_Halide&amp;diff=967"/>
		<updated>2018-01-28T20:46:07Z</updated>

		<summary type="html">&lt;p&gt;Kimyease: /* 2-bromobutane synthesis (Yeaseul Kim) */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Main_Page]]&lt;br /&gt;
__TOC__&lt;br /&gt;
&lt;br /&gt;
== Jacob Morsch ==&lt;br /&gt;
&lt;br /&gt;
[[File:Alkyl_halide.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Acetyl chloride (Imany Noel) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Alkyl_Halide.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
A reaction of acetic acid with thionyl chloride to form acetyl chloride.&lt;br /&gt;
&lt;br /&gt;
== 2-bromobutane synthesis (Yeaseul Kim) ==&lt;br /&gt;
&lt;br /&gt;
[[File: 2-bromobutane_synthesis.png|1100px]]&lt;/div&gt;</summary>
		<author><name>Kimyease</name></author>
	</entry>
	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Alkyl_Halide&amp;diff=966</id>
		<title>Talk:Alkyl Halide</title>
		<link rel="alternate" type="text/html" href="http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Alkyl_Halide&amp;diff=966"/>
		<updated>2018-01-28T20:45:25Z</updated>

		<summary type="html">&lt;p&gt;Kimyease: /* 2-bromobutane synthesis (Yeaseul Kim) */ new section&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Main_Page]]&lt;br /&gt;
__TOC__&lt;br /&gt;
&lt;br /&gt;
== Jacob Morsch ==&lt;br /&gt;
&lt;br /&gt;
[[File:Alkyl_halide.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Acetyl chloride (Imany Noel) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Alkyl_Halide.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
A reaction of acetic acid with thionyl chloride to form acetyl chloride.&lt;br /&gt;
&lt;br /&gt;
== 2-bromobutane synthesis (Yeaseul Kim) ==&lt;br /&gt;
&lt;br /&gt;
[[File: bromobutane_synthesis.png|1100px]]&lt;/div&gt;</summary>
		<author><name>Kimyease</name></author>
	</entry>
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