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	<id>http://organicchem.sites.grinnell.edu/wiki/spring19/api.php?action=feedcontributions&amp;feedformat=atom&amp;user=Neylanky</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=Neylanky"/>
	<link rel="alternate" type="text/html" href="http://organicchem.sites.grinnell.edu/wiki/spring19/Special:Contributions/Neylanky"/>
	<updated>2026-11-06T06:36:48Z</updated>
	<subtitle>User contributions</subtitle>
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	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Alcohol&amp;diff=799</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=799"/>
		<updated>2017-05-09T23:38:53Z</updated>

		<summary type="html">&lt;p&gt;Neylanky: /* Reduction to alkane */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Main_Page]]&lt;br /&gt;
__TOC__&lt;br /&gt;
&lt;br /&gt;
[[File:Tert-Butyl Alcohol.png|100px.]]&lt;br /&gt;
&lt;br /&gt;
== DeRoche Grignard Reaction ==&lt;br /&gt;
&lt;br /&gt;
[[File:Grignard_Reaction.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Ethanol (Beth Ann Hansen) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Ester_to_Alcohol_with_LiAlH4.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Butanol Ky-Sean Johnson ==&lt;br /&gt;
&lt;br /&gt;
[[File:AlcoholJohnson.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Primary alcohol from acid chloride (Katie McDonald) ==&lt;br /&gt;
&lt;br /&gt;
[[File:OchemWiki1.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Formation of cyclopentane-1,2-diol (Hannah Hong) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Alcohol_formation.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Hydroboration reaction (Lila Cardozo) ==&lt;br /&gt;
&lt;br /&gt;
Hyrdoboration reaction of 1-methylcyclopent-1-ene to produce 2-methylcyclopentan-1-ol&lt;br /&gt;
[[File:Wiki2_alcohol.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Ozonolysis (Xiaobo Sun) ==&lt;br /&gt;
&lt;br /&gt;
[[File: Untitled_Document-1.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== HG(OAc)2 Alcohol ==&lt;br /&gt;
&lt;br /&gt;
[[File:Screen_Shot_2017-02-19_at_9.01.41_PM.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Formation of 2-ethylbutane-1,2-diol (Alfredo) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Formation_of_2-ethylbutane-1,2-diol_(Alfredo).png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Indole Reaction (Lila Cardozo) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Wikiindole.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Reduction of secondary alcohol to alkane (Kyra Neylan)==&lt;br /&gt;
&lt;br /&gt;
Reduction of secondary alcohol propan-2-ol to propane.&lt;br /&gt;
&lt;br /&gt;
[[File:Alcohol.png|600px]]&lt;/div&gt;</summary>
		<author><name>Neylanky</name></author>
	</entry>
	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Alcohol&amp;diff=798</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=798"/>
		<updated>2017-05-09T23:37:50Z</updated>

		<summary type="html">&lt;p&gt;Neylanky: /* Reduction to alkane */ new section&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Main_Page]]&lt;br /&gt;
__TOC__&lt;br /&gt;
&lt;br /&gt;
[[File:Tert-Butyl Alcohol.png|100px.]]&lt;br /&gt;
&lt;br /&gt;
== DeRoche Grignard Reaction ==&lt;br /&gt;
&lt;br /&gt;
[[File:Grignard_Reaction.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Ethanol (Beth Ann Hansen) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Ester_to_Alcohol_with_LiAlH4.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Butanol Ky-Sean Johnson ==&lt;br /&gt;
&lt;br /&gt;
[[File:AlcoholJohnson.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Primary alcohol from acid chloride (Katie McDonald) ==&lt;br /&gt;
&lt;br /&gt;
[[File:OchemWiki1.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Formation of cyclopentane-1,2-diol (Hannah Hong) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Alcohol_formation.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Hydroboration reaction (Lila Cardozo) ==&lt;br /&gt;
&lt;br /&gt;
Hyrdoboration reaction of 1-methylcyclopent-1-ene to produce 2-methylcyclopentan-1-ol&lt;br /&gt;
[[File:Wiki2_alcohol.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Ozonolysis (Xiaobo Sun) ==&lt;br /&gt;
&lt;br /&gt;
[[File: Untitled_Document-1.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== HG(OAc)2 Alcohol ==&lt;br /&gt;
&lt;br /&gt;
[[File:Screen_Shot_2017-02-19_at_9.01.41_PM.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Formation of 2-ethylbutane-1,2-diol (Alfredo) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Formation_of_2-ethylbutane-1,2-diol_(Alfredo).png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Indole Reaction (Lila Cardozo) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Wikiindole.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Reduction to alkane ==&lt;br /&gt;
&lt;br /&gt;
Reduction of propan-2-ol to propane.&lt;br /&gt;
&lt;br /&gt;
[[File:Alcohol.png|600px]]&lt;/div&gt;</summary>
		<author><name>Neylanky</name></author>
	</entry>
	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Alpha,_beta_unsaturated_ketone&amp;diff=796</id>
		<title>Talk:Alpha, beta unsaturated ketone</title>
		<link rel="alternate" type="text/html" href="http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Alpha,_beta_unsaturated_ketone&amp;diff=796"/>
		<updated>2017-05-09T23:28:52Z</updated>

		<summary type="html">&lt;p&gt;Neylanky: /* Alpha-beta unsaturated ketone (Kyra Neylan) */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Main_Page]]&lt;br /&gt;
__TOC__&lt;br /&gt;
&lt;br /&gt;
== Synthesis of Alpha, Beta Unsaturated Ketone - Emma Olson ==&lt;br /&gt;
&lt;br /&gt;
[[File:Alpha_Beta_Unsaturated_Ketone.png|600px]]&lt;br /&gt;
&lt;br /&gt;
== Aldol condensation to alpha, beta unsaturated ketone (Beth Ann Hansen) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Unsaturated_ketone.png|500px]]&lt;br /&gt;
&lt;br /&gt;
== Alpha, Beta Unsaturated Ketone (Ian Windham) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Alpha_Beta_Unsaturated_Ketone.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Alpha, beta unsaturated ketone (Kyra Neylan) ==&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[File:Alpha-beta_unsaturated_ketone.png|700px]]&lt;/div&gt;</summary>
		<author><name>Neylanky</name></author>
	</entry>
	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Alpha,_beta_unsaturated_ketone&amp;diff=795</id>
		<title>Talk:Alpha, beta unsaturated ketone</title>
		<link rel="alternate" type="text/html" href="http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Alpha,_beta_unsaturated_ketone&amp;diff=795"/>
		<updated>2017-05-09T23:28:31Z</updated>

		<summary type="html">&lt;p&gt;Neylanky: /* Alpha-beta unsaturated ketone (Kyra Neylan) */ new section&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Main_Page]]&lt;br /&gt;
__TOC__&lt;br /&gt;
&lt;br /&gt;
== Synthesis of Alpha, Beta Unsaturated Ketone - Emma Olson ==&lt;br /&gt;
&lt;br /&gt;
[[File:Alpha_Beta_Unsaturated_Ketone.png|600px]]&lt;br /&gt;
&lt;br /&gt;
== Aldol condensation to alpha, beta unsaturated ketone (Beth Ann Hansen) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Unsaturated_ketone.png|500px]]&lt;br /&gt;
&lt;br /&gt;
== Alpha, Beta Unsaturated Ketone (Ian Windham) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Alpha_Beta_Unsaturated_Ketone.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Alpha-beta unsaturated ketone (Kyra Neylan) ==&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[File:Alpha-beta_unsaturated_ketone.png|700px]]&lt;/div&gt;</summary>
		<author><name>Neylanky</name></author>
	</entry>
	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Ketone&amp;diff=694</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=694"/>
		<updated>2017-02-17T02:10:41Z</updated>

		<summary type="html">&lt;p&gt;Neylanky: /* Dimethyl ketone by ozonolysis (Kyra Neylan) */ new section&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Main_Page]]&lt;br /&gt;
__TOC__&lt;br /&gt;
&lt;br /&gt;
== Hydrolysis to from Acetone ==&lt;br /&gt;
&lt;br /&gt;
Heather Roesch[[File:Ketone (Acetone).png]]&lt;br /&gt;
&lt;br /&gt;
== Rachel Tappe: Oxidation of an alcohol into a ketone ==&lt;br /&gt;
&lt;br /&gt;
[[File:Screenshot_2017-01-28_15.16.43.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Frieden Crafts Acylation  (Katie McDonald) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Friedel_Crafts_Acylation.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Nucleophilic Addition to Alkyne (Lauren MacKenzie ==&lt;br /&gt;
&lt;br /&gt;
[[File:Rxn_2.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
The product easily transforms between the keto and enol forms (hence the double arrows), but the keto form is predominant.&lt;br /&gt;
&lt;br /&gt;
== Dimethyl ketone by ozonolysis (Kyra Neylan) ==&lt;br /&gt;
&lt;br /&gt;
2,3-dimethylbut-2-ene reacts with ozone and then dimethyl sulfide to form dimethylketone (acetone).&lt;br /&gt;
[[File:Ozonolysis.png|900px]]&lt;/div&gt;</summary>
		<author><name>Neylanky</name></author>
	</entry>
	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Carboxylic_Acid&amp;diff=607</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=607"/>
		<updated>2017-01-25T00:51:19Z</updated>

		<summary type="html">&lt;p&gt;Neylanky: /* Cyanonitrile to Carboxylic Acid (Kyra Neylan) */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Main_Page]]&lt;br /&gt;
__TOC__&lt;br /&gt;
&lt;br /&gt;
== CO2 to Carboxylic Acid (Lauren MacKenzie ==&lt;br /&gt;
&lt;br /&gt;
In this reaction, an organometallic reagent reacts with CO2 (in a solution of diethyl ether) to create an intermediate, which reacts with H3O+ to create a carboxylic acid. &lt;br /&gt;
&lt;br /&gt;
[[File: CO2_to_Carboxylic_Acid.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Cyanonitrile to Carboxylic Acid (Kyra Neylan) ==&lt;br /&gt;
Reaction of propanonitrile in water with acid and heat to form propanoic acid and ammonium.&lt;br /&gt;
[[File: Cyanonitrile_to_Carboxylic_Acid_(Kyra_Neylan).png|1100px]]&lt;/div&gt;</summary>
		<author><name>Neylanky</name></author>
	</entry>
	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Carboxylic_Acid&amp;diff=606</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=606"/>
		<updated>2017-01-25T00:49:50Z</updated>

		<summary type="html">&lt;p&gt;Neylanky: /* Cyanonitrile to Carboxylic Acid (Kyra Neylan) */ new section&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Main_Page]]&lt;br /&gt;
__TOC__&lt;br /&gt;
&lt;br /&gt;
== CO2 to Carboxylic Acid (Lauren MacKenzie ==&lt;br /&gt;
&lt;br /&gt;
In this reaction, an organometallic reagent reacts with CO2 (in a solution of diethyl ether) to create an intermediate, which reacts with H3O+ to create a carboxylic acid. &lt;br /&gt;
&lt;br /&gt;
[[File: CO2_to_Carboxylic_Acid.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Cyanonitrile to Carboxylic Acid (Kyra Neylan) ==&lt;br /&gt;
&lt;br /&gt;
[[File: Cyanonitrile_to_Carboxylic_Acid_(Kyra_Neylan).png|1100px]]&lt;/div&gt;</summary>
		<author><name>Neylanky</name></author>
	</entry>
</feed>