http://organicchem.sites.grinnell.edu/wiki/spring19/api.php?action=feedcontributions&feedformat=atom&user=Mackenzi 2026-11-06T06:36:35Z User contributions MediaWiki 1.45.3 http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Ester&diff=809 2017-05-10T03:04:26Z

<p>Mackenzi: /* Polyester Synthesis through Ester linkages (Lauren MacKenzie) */ new section</p> <hr /> <div>[[Main_Page]]<br /> __TOC__<br /> <br /> == Formation of isobutyl propionate (Yun Tang) ==<br /> <br /> [[File:Formation of isobutyl propionate (Yun Tang).png|1100px]]<br /> <br /> == Hellweg Reaction of Carboxylic Acid and Alcohol to form an Ester ==<br /> <br /> [[File:Hellweg_reaction_of_carboxylic_acid_and_alcohol_to_form_an_ester.png|1100px]]<br /> <br /> == Formation of propyl butyrate (Jordan Hamilton) ==<br /> <br /> [[File:ESTER.png|1100px]]<br /> <br /> == Ketone to ester (Daniel Hwang) ==<br /> <br /> [[File:Ketone_to_ester.png|100px.]]<br /> <br /> == Claisen Condensation (Liangchen Liu) ==<br /> <br /> [[File:Wiki3.png|1100px]]<br /> <br /> == Polyester Synthesis through Ester linkages (Lauren MacKenzie) ==<br /> <br /> [[File:Rxn_4.png|1000px]]</div>

Mackenzi http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Alkene&diff=807 2017-05-10T02:46:35Z

<p>Mackenzi: /* Aldol Condensation (Lauren MacKenzie) */ new section</p> <hr /> <div>[[Main_Page]]<br /> __TOC__<br /> <br /> == Wittig Reaction (Nora Madrigal) ==<br /> <br /> Acetone reacts with a triphenyl phosphonium ylid to form 2-methylpropene and triphenylphosphine oxide (synthesis of an alkene from a ketone).<br /> [[File:Wittig_Rxn_Madrigal.png|1100px]]<br /> <br /> == Elimination Reaction (Xiaobo Sun) ==<br /> <br /> [[File:Elimination_reaction.png|1000px]]<br /> <br /> == Dehydration of an Alcohol (Heather Roesch) ==<br /> <br /> [[File:Dehydration_of_Alcohol.png]]|1100px<br /> <br /> == Diels Alder Rxn ==<br /> <br /> [[File:Diels_Alder_Rxn.png|1100px]]<br /> <br /> == Reduction of an Alkyne to an Alkene (Nora Madrigal) ==<br /> <br /> [[File:Lindlar_catalyst_2.png|1100px]]<br /> <br /> == Reduction of an Alkyne to a trans Alkene (Xiaobo Sun) ==<br /> <br /> [[File:Alkene.png|1100px]]<br /> <br /> == Aldol Condensation (Lauren MacKenzie) ==<br /> <br /> [[File:Rxn_3.png|1000px]]</div>

Mackenzi http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Ketone&diff=690 2017-02-16T04:27:39Z

<p>Mackenzi: /* Nucleophilic Addition to Alkyne (Lauren MacKenzie */ 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.</div>

Mackenzi http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Carboxylic_Acid&diff=597 2017-01-24T03:35:14Z

<p>Mackenzi: /* CO2 to Carboxylic Acid (Lauren MacKenzie */ 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]]</div>

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