http://organicchem.sites.grinnell.edu/wiki/spring19/api.php?action=feedcontributions&feedformat=atom&user=Luzhiye 2026-11-06T06:18:22Z User contributions MediaWiki 1.45.3 http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Carboxylic_Acid&diff=814 2017-05-10T03:32:13Z

<p>Luzhiye: /* Decarboxylation of 1,3-dicarbonyl to form carboxylic acid (Zhiye Lu) */ new section</p> <hr /> <div>[[Main_Page]]<br /> __TOC__<br /> <br /> == CO2 to Carboxylic Acid (Lauren MacKenzie ==<br /> <br /> 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. <br /> <br /> [[File: CO2_to_Carboxylic_Acid.png|1100px]]<br /> <br /> == Cyanonitrile to Carboxylic Acid (Kyra Neylan) ==<br /> Reaction of propanonitrile in water with acid and heat to form propanoic acid and ammonium.<br /> [[File: Cyanonitrile_to_Carboxylic_Acid_(Kyra_Neylan).png|1100px]]<br /> <br /> == Chromium Trioxide to Carboxylic Acid (Noah Fluharty) ==<br /> <br /> [[File:Chem_Wiki_1.png|1100px]]<br /> <br /> == Ester Hydrolysis to Form Carboxylic Acid (Zhiye Lu) ==<br /> <br /> Ester hydrolysis with acid catalysis to form carboxylic acid.<br /> [[File:WIKI.png|1100px]]<br /> <br /> == Aldehyde to Carboxylic Acid with Nitrile and Acid (Beth Ann Hansen) ==<br /> <br /> [[File:Aldehyde_to_Carboxylic_Acid_with_Nitrile_and_Acid.png|1100px]]<br /> <br /> == Decarboxylation of 1,3-dicarbonyl to form carboxylic acid (Zhiye Lu) ==<br /> <br /> [[File:carboxylic acid.png|1100px]]</div>

Luzhiye http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Ketone&diff=813 2017-05-10T03:30:37Z

<p>Luzhiye: /* Decarboxylation of 1,3-dicarbonyl to form ketone (Zhiye Lu) */</p> <hr /> <div>[[Main_Page]]<br /> __TOC__<br /> <br /> == Hydrolysis to from Acetone ==<br /> <br /> Heather Roesch[[File:Ketone (Acetone).png]]<br /> <br /> == Rachel Tappe: Oxidation of an alcohol into a ketone ==<br /> <br /> [[File:Screenshot_2017-01-28_15.16.43.png|1100px]]<br /> <br /> == Frieden Crafts Acylation (Katie McDonald) ==<br /> <br /> [[File:Friedel_Crafts_Acylation.png|1100px]]<br /> <br /> == Nucleophilic Addition to Alkyne (Lauren MacKenzie ==<br /> <br /> [[File:Rxn_2.png|1100px]]<br /> <br /> The product easily transforms between the keto and enol forms (hence the double arrows), but the keto form is predominant.<br /> <br /> == Dimethyl ketone by ozonolysis (Kyra Neylan) ==<br /> <br /> 2,3-dimethylbut-2-ene reacts with ozone and then dimethyl sulfide to form dimethylketone (acetone).<br /> [[File:Ozonolysis.png|900px]]<br /> <br /> == The Clemmensen Reduction Rong Guo==<br /> <br /> [[File:The Clemmensen Reduction Rong Guo.png|500px]]<br /> <br /> == Acetal Formation (Ky-Sean Johnson) ==<br /> <br /> [[File:AcetalJohnson.png|1100px]]<br /> <br /> == Heterocycle ketone addition (Lila Cardozo) ==<br /> <br /> [[File:Wiki4_heterocycles.png|1100px]]<br /> <br /> == Michael Condensation (Liangchen Liu) ==<br /> <br /> [[File:Wiki4.png|1100px]]<br /> <br /> == Swern Oxidation of Primary Alcohol (Noah Fluharty) ==<br /> <br /> [[File:Reaction_4.png|1100px]]<br /> <br /> == Decarboxylation of 1,3-dicarbonyl to form ketone (Zhiye Lu) ==<br /> <br /> [[File:ketone.png|1100px]]</div>

Luzhiye http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Ketone&diff=812 2017-05-10T03:30:06Z

<p>Luzhiye: /* Decarboxylation of 1,3-dicarbonyl to form ketone (Zhiye Lu) */ new section</p> <hr /> <div>[[Main_Page]]<br /> __TOC__<br /> <br /> == Hydrolysis to from Acetone ==<br /> <br /> Heather Roesch[[File:Ketone (Acetone).png]]<br /> <br /> == Rachel Tappe: Oxidation of an alcohol into a ketone ==<br /> <br /> [[File:Screenshot_2017-01-28_15.16.43.png|1100px]]<br /> <br /> == Frieden Crafts Acylation (Katie McDonald) ==<br /> <br /> [[File:Friedel_Crafts_Acylation.png|1100px]]<br /> <br /> == Nucleophilic Addition to Alkyne (Lauren MacKenzie ==<br /> <br /> [[File:Rxn_2.png|1100px]]<br /> <br /> The product easily transforms between the keto and enol forms (hence the double arrows), but the keto form is predominant.<br /> <br /> == Dimethyl ketone by ozonolysis (Kyra Neylan) ==<br /> <br /> 2,3-dimethylbut-2-ene reacts with ozone and then dimethyl sulfide to form dimethylketone (acetone).<br /> [[File:Ozonolysis.png|900px]]<br /> <br /> == The Clemmensen Reduction Rong Guo==<br /> <br /> [[File:The Clemmensen Reduction Rong Guo.png|500px]]<br /> <br /> == Acetal Formation (Ky-Sean Johnson) ==<br /> <br /> [[File:AcetalJohnson.png|1100px]]<br /> <br /> == Heterocycle ketone addition (Lila Cardozo) ==<br /> <br /> [[File:Wiki4_heterocycles.png|1100px]]<br /> <br /> == Michael Condensation (Liangchen Liu) ==<br /> <br /> [[File:Wiki4.png|1100px]]<br /> <br /> == Swern Oxidation of Primary Alcohol (Noah Fluharty) ==<br /> <br /> [[File:Reaction_4.png|1100px]]<br /> <br /> == Decarboxylation of 1,3-dicarbonyl to form ketone (Zhiye Lu) ==<br /> <br /> [[File:ketone.jpg|1100px]]</div>

Luzhiye http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Aromatic_amine&diff=705 2017-02-19T17:29:30Z

<p>Luzhiye: /* Elimination-Addition Reaction to Synthesize Toluidine (Zhiye Lu) */ new section</p> <hr /> <div>[[Main_Page]]<br /> __TOC__<br /> <br /> == Conversion of Nitro Group to Amine (Nora Madrigal) ==<br /> <br /> [[File:Nitro_to_amine.png|1100px]]<br /> The nitro group on a benzene ring reacts with tin and hydrochloric acid to form an amine.<br /> <br /> == Elimination-Addition Reaction to Synthesize Toluidine (Zhiye Lu) ==<br /> <br /> [[File:Zhiye_Lu.png|1100px]]</div>

Luzhiye http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Carboxylic_Acid&diff=632 2017-01-29T08:26:36Z

<p>Luzhiye: /* Ester Hydrolysis to Form Carboxylic Acid (Zhiye Lu) */ new section</p> <hr /> <div>[[Main_Page]]<br /> __TOC__<br /> <br /> == CO2 to Carboxylic Acid (Lauren MacKenzie ==<br /> <br /> 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. <br /> <br /> [[File: CO2_to_Carboxylic_Acid.png|1100px]]<br /> <br /> == Cyanonitrile to Carboxylic Acid (Kyra Neylan) ==<br /> Reaction of propanonitrile in water with acid and heat to form propanoic acid and ammonium.<br /> [[File: Cyanonitrile_to_Carboxylic_Acid_(Kyra_Neylan).png|1100px]]<br /> <br /> == Chromium Trioxide to Carboxylic Acid (Noah Fluharty) ==<br /> <br /> [[File:Chem_Wiki_1.png|1100px]]<br /> <br /> == Ester Hydrolysis to Form Carboxylic Acid (Zhiye Lu) ==<br /> <br /> Ester hydrolysis with acid catalysis to form carboxylic acid.<br /> [[File:WIKI.png|1100px]]</div>

Luzhiye