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	<id>http://organicchem.sites.grinnell.edu/wiki/spring19/api.php?action=feedcontributions&amp;feedformat=atom&amp;user=Merschja</id>
	<title>Organic Chemistry Wiki Spring 2019 - User contributions [en]</title>
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	<updated>2026-11-06T06:16:48Z</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=1134</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=1134"/>
		<updated>2018-05-11T04:37:58Z</updated>

		<summary type="html">&lt;p&gt;Merschja: /* Polyethylene Radical Polymerization (James Mersch) */ 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;br /&gt;
&lt;br /&gt;
== Synthesis of 4-methyl-pentan-2-one (Ed Lopatto) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Alkane_lopatto_wiki.png|500px]]&lt;br /&gt;
&lt;br /&gt;
== Birch Reduction Bretta McCall[[File:Birch.png]] ==&lt;br /&gt;
&lt;br /&gt;
Birch Reduction&lt;br /&gt;
&lt;br /&gt;
== Raney Nickel (Xinming Li) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Raney nickel.png|800px]]&lt;br /&gt;
&lt;br /&gt;
== Polyethylene Radical Polymerization (James Mersch) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Wiki_thing_2.png|1000px]]&lt;/div&gt;</summary>
		<author><name>Merschja</name></author>
	</entry>
	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Alcohol&amp;diff=1132</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=1132"/>
		<updated>2018-05-11T04:26:55Z</updated>

		<summary type="html">&lt;p&gt;Merschja: /* Glucose Reduction (James Mersch) */ 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;br /&gt;
&lt;br /&gt;
== Baylis-Hilman Reaction (Nannan Ji) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Baylis-Hilman_Reaction.png]]&lt;br /&gt;
&lt;br /&gt;
== (1H-indol-3-yl)methanol ==&lt;br /&gt;
&lt;br /&gt;
[[File: Aromatic_Substitution.png|900px]]&lt;br /&gt;
&lt;br /&gt;
== Glucose Reduction (James Mersch) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Wiki_thing.png|1000px]]&lt;/div&gt;</summary>
		<author><name>Merschja</name></author>
	</entry>
	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Alkyl_Halide&amp;diff=1028</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=1028"/>
		<updated>2018-02-06T23:16:42Z</updated>

		<summary type="html">&lt;p&gt;Merschja: /* Bromoacetone (James Mersch) */ 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: 2-bromobutane_synthesis.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Bromoacetone (James Mersch) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Bromoacetone (James Mersch).png|1100px]]&lt;/div&gt;</summary>
		<author><name>Merschja</name></author>
	</entry>
	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Carboxylic_Acid&amp;diff=983</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=983"/>
		<updated>2018-01-30T00:49:03Z</updated>

		<summary type="html">&lt;p&gt;Merschja: /* Propanoic Acid (James Mersch) */ 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|1100px]]&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;/div&gt;</summary>
		<author><name>Merschja</name></author>
	</entry>
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