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	<id>http://organicchem.sites.grinnell.edu/wiki/spring19/api.php?action=feedcontributions&amp;feedformat=atom&amp;user=Recordma</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=Recordma"/>
	<link rel="alternate" type="text/html" href="http://organicchem.sites.grinnell.edu/wiki/spring19/Special:Contributions/Recordma"/>
	<updated>2026-11-06T06:16:06Z</updated>
	<subtitle>User contributions</subtitle>
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	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Amine&amp;diff=1139</id>
		<title>Talk:Amine</title>
		<link rel="alternate" type="text/html" href="http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Amine&amp;diff=1139"/>
		<updated>2018-05-11T05:31:29Z</updated>

		<summary type="html">&lt;p&gt;Recordma: /* Strecker Synthesis (Matthew Record) */ new section&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;== N-ethylcyclohexanimine (Maverick Zhang) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Untitled_Document-1.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
Cyclohexanone reacts with ethanamine in acidic condition to form N-ethylcyclohexanimine.&lt;br /&gt;
&lt;br /&gt;
== N-methyl-1-phenylmethanamine (Michael Hewitt) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Screen_Shot_2018-02-04_at_7.43.06_PM.png]]&lt;br /&gt;
&lt;br /&gt;
== Enamine formation (Edward Lopatto) ==&lt;br /&gt;
&lt;br /&gt;
Reaction of a second-degree amine with a ketone to form an enamine.&lt;br /&gt;
[[File:Enamine_formation.png|800px]]&lt;br /&gt;
&lt;br /&gt;
== Butanamine (Matthew Palmeri) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Butanamine_Wiki_entry_2.png|1000px]]&lt;br /&gt;
&lt;br /&gt;
== Formation of Amine from Nitro group (Kelsey Zhang) ==&lt;br /&gt;
&lt;br /&gt;
[[File: Reduction_of_amide.png|1100px]]&lt;br /&gt;
The formation of Amine from Nitro group with Tin in acidic condition&lt;br /&gt;
&lt;br /&gt;
==2-aminobutanal (Mikayla Kricfalusi)==&lt;br /&gt;
&lt;br /&gt;
[[File:2-aminobutanal (Mikayla Kricfalusi).png|1000px]]&lt;br /&gt;
&lt;br /&gt;
== Second synthesis of 2-aminobutanal (Mikayla Kricfalusi)==&lt;br /&gt;
&lt;br /&gt;
[[File:Amino_acid_again.png|1000px]]&lt;br /&gt;
&lt;br /&gt;
== Strecker Synthesis (Matthew Record) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Strecker_Synthesis.png|1100px]]&lt;/div&gt;</summary>
		<author><name>Recordma</name></author>
	</entry>
	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Ketone&amp;diff=1137</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=1137"/>
		<updated>2018-05-11T05:20:45Z</updated>

		<summary type="html">&lt;p&gt;Recordma: /* Claisen Condensation (Matthew Record) */&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;br /&gt;
&lt;br /&gt;
== Acetone (Imany Noel) ==&lt;br /&gt;
&lt;br /&gt;
[[File:PCC_copy.jpeg]]&lt;br /&gt;
&lt;br /&gt;
Oxidation of an alcohol to a ketone.&lt;br /&gt;
&lt;br /&gt;
== Formation of ketone from beta-ketoester by decarboxylation (Kelsey Zhang) ==&lt;br /&gt;
&lt;br /&gt;
[[File: Ketone_from_ketoester.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Chalcone (Maverick) ==&lt;br /&gt;
&lt;br /&gt;
[[File: Chalcone.png|900px]]&lt;br /&gt;
&lt;br /&gt;
== Claisen Condensation (Matthew Record) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Claisen_condensation.png|1100px]]&lt;/div&gt;</summary>
		<author><name>Recordma</name></author>
	</entry>
	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Ketone&amp;diff=1136</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=1136"/>
		<updated>2018-05-11T05:19:46Z</updated>

		<summary type="html">&lt;p&gt;Recordma: /* Claisen Condensation (Matthew Record) */ 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;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;br /&gt;
&lt;br /&gt;
== Acetone (Imany Noel) ==&lt;br /&gt;
&lt;br /&gt;
[[File:PCC_copy.jpeg]]&lt;br /&gt;
&lt;br /&gt;
Oxidation of an alcohol to a ketone.&lt;br /&gt;
&lt;br /&gt;
== Formation of ketone from beta-ketoester by decarboxylation (Kelsey Zhang) ==&lt;br /&gt;
&lt;br /&gt;
[[File: Ketone_from_ketoester.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Chalcone (Maverick) ==&lt;br /&gt;
&lt;br /&gt;
[[File: Chalcone.png|900px]]&lt;br /&gt;
&lt;br /&gt;
== Claisen Condensation (Matthew Record) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Claisen_condensation.png|100px]]&lt;/div&gt;</summary>
		<author><name>Recordma</name></author>
	</entry>
	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Carboxylic_Acid&amp;diff=1002</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=1002"/>
		<updated>2018-02-04T21:23:53Z</updated>

		<summary type="html">&lt;p&gt;Recordma: /* Base Promoted Halogenation (Matthew Record) */ 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;br /&gt;
&lt;br /&gt;
== Base Promoted Halogenation (Matthew Record) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Base_promoted_halogenation.png|1100px]]&lt;/div&gt;</summary>
		<author><name>Recordma</name></author>
	</entry>
	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Ester&amp;diff=904</id>
		<title>Talk:Ester</title>
		<link rel="alternate" type="text/html" href="http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Ester&amp;diff=904"/>
		<updated>2018-01-23T01:06:14Z</updated>

		<summary type="html">&lt;p&gt;Recordma: /* Fischer Esterification (Matthew Record) */ new section&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Main_Page]]&lt;br /&gt;
__TOC__&lt;br /&gt;
&lt;br /&gt;
== Ester Grignard Reaction in Acid (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;
== Fischer Esterification (Matthew Record) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Ester2.png|1100px]]&lt;/div&gt;</summary>
		<author><name>Recordma</name></author>
	</entry>
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