http://organicchem.sites.grinnell.edu/wiki/spring19/api.php?action=feedcontributions&feedformat=atom&user=Herringi 2026-11-06T01:00:35Z User contributions MediaWiki 1.45.3 http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Ketone&diff=1464 2019-05-10T21:25:17Z

<p>Herringi: /* Converting ester to ketone */</p> <hr /> <div>[[Main_Page]]<br /> __TOC__<br /> <br /> == Synthesis of a Ketone from an Acyl Chloride using a Gilman reagent (Nichole Hannan) ==<br /> <br /> [[File:KetoneSynthesis.png|500px]]<br /> <br /> == Synthesis of ketone from a secondary alcohol (Chloe Wu) ==<br /> <br /> [[File:Ketone.png|500px]]<br /> <br /> == Acetic Anhydride and a Grignard Reagent react with an acid workup to produce Acetic Acid and Acetophenone (Malia Wells) ==<br /> <br /> [[File:OChem_2_WIKI_Reaction_Ketone.png|1000px]]<br /> <br /> == Synthesis of ketone from a secondary alcohol (Emily Mamrak) ==<br /> <br /> [[File:cyclohexanone.png|500px]]<br /> <br /> == Synthesis of 2-butanone from 1-butyne (Madison Howe) ==<br /> <br /> [[File:Ketone_synthesis.png|1000px]]<br /> <br /> == Electrophilic alkene and soft nucleophile - Klarie Li ==<br /> <br /> [[File:Electrophilic_alkene_and_soft_nuclephile.png|600px]]<br /> <br /> == Jone's Oxidation-Steven Sharpe ==<br /> <br /> [[File:Jone's Oxidation.PNG]]<br /> <br /> The Jone's Oxidation provides an easy and relatively cheap way to oxidize an secondary alcohol into a ketone. When a primary alcohol is reduced, it forms a carboxylic acid.<br /> <br /> == synthesis of 4-(4-methoxyphenyl)-3-Buten-2-one from 4-methoxy-benzaldehyde and acetone from aldol addition - ( Xuanhe Chen ) ==<br /> <br /> [[File:Step2-1.jpg|1000px]]<br /> <br /> == Synthesis of 1-(p-tolyl)propan-2-one from 1-bromo-4-methylbenzene using Potassium 2-oxopropan-1-ide (Kyle Dixon-Anderson) ==<br /> <br /> [[File:Aromatic+ketone synthesis.jpg]]<br /> <br /> == Synthesis of Ketone by Fredyl-Craft Acylation (Amelia Zoernig) ==<br /> <br /> [[File:Fcaketone.JPG]]<br /> <br /> == Converting ester to ketone (Isaias Herring) ==<br /> <br /> [[File:Converting_ester_to_ketone.PNG|1100px]]</div>

Herringi http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Ketone&diff=1463 2019-05-10T21:24:57Z

<p>Herringi: /* Converting ester to ketone */ new section</p> <hr /> <div>[[Main_Page]]<br /> __TOC__<br /> <br /> == Synthesis of a Ketone from an Acyl Chloride using a Gilman reagent (Nichole Hannan) ==<br /> <br /> [[File:KetoneSynthesis.png|500px]]<br /> <br /> == Synthesis of ketone from a secondary alcohol (Chloe Wu) ==<br /> <br /> [[File:Ketone.png|500px]]<br /> <br /> == Acetic Anhydride and a Grignard Reagent react with an acid workup to produce Acetic Acid and Acetophenone (Malia Wells) ==<br /> <br /> [[File:OChem_2_WIKI_Reaction_Ketone.png|1000px]]<br /> <br /> == Synthesis of ketone from a secondary alcohol (Emily Mamrak) ==<br /> <br /> [[File:cyclohexanone.png|500px]]<br /> <br /> == Synthesis of 2-butanone from 1-butyne (Madison Howe) ==<br /> <br /> [[File:Ketone_synthesis.png|1000px]]<br /> <br /> == Electrophilic alkene and soft nucleophile - Klarie Li ==<br /> <br /> [[File:Electrophilic_alkene_and_soft_nuclephile.png|600px]]<br /> <br /> == Jone's Oxidation-Steven Sharpe ==<br /> <br /> [[File:Jone's Oxidation.PNG]]<br /> <br /> The Jone's Oxidation provides an easy and relatively cheap way to oxidize an secondary alcohol into a ketone. When a primary alcohol is reduced, it forms a carboxylic acid.<br /> <br /> == synthesis of 4-(4-methoxyphenyl)-3-Buten-2-one from 4-methoxy-benzaldehyde and acetone from aldol addition - ( Xuanhe Chen ) ==<br /> <br /> [[File:Step2-1.jpg|1000px]]<br /> <br /> == Synthesis of 1-(p-tolyl)propan-2-one from 1-bromo-4-methylbenzene using Potassium 2-oxopropan-1-ide (Kyle Dixon-Anderson) ==<br /> <br /> [[File:Aromatic+ketone synthesis.jpg]]<br /> <br /> == Synthesis of Ketone by Fredyl-Craft Acylation (Amelia Zoernig) ==<br /> <br /> [[File:Fcaketone.JPG]]<br /> <br /> == Converting ester to ketone ==<br /> <br /> [[File:Converting_ester_to_ketone.PNG|1100px]]</div>

Herringi http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=File:Converting_ester_to_ketone.PNG&diff=1462 2019-05-10T21:20:19Z

<p>Herringi: </p> <hr /> <div></div>

Herringi http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Alpha,_beta_unsaturated_ester&diff=1338 2019-02-20T23:04:12Z

<p>Herringi: /* Isaias Herring- Alpha, beta, unsaturated ester */ new section</p> <hr /> <div>[[Main_Page]]<br /> __TOC__<br /> <br /> == Isaias Herring- Alpha, beta, unsaturated ester ==<br /> <br /> [[File:Wikiassignment.png|1100px]]</div>

Herringi http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=File:Wikiassignment.png&diff=1337 2019-02-20T23:01:43Z

<p>Herringi: </p> <hr /> <div></div>

Herringi http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Alkyne&diff=1257 2019-01-27T22:12:01Z

<p>Herringi: /* HerringI Corey-Fuchs Reaction 1000px */ new section</p> <hr /> <div>[[Main_Page]]<br /> __TOC__<br /> <br /> == HerringI Corey-Fuchs Reaction [[File:Herringi__Corey-Fuchs_reaction1.png|1000px]] ==<br /> <br /> Corey-Fuchs reaction for alkyne formation.</div>

Herringi http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=File:Herringi_Corey-Fuchs_reaction1.png&diff=1256 2019-01-27T22:08:26Z

<p>Herringi: </p> <hr /> <div></div>

Herringi http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=File:Herringi_alkyne_synthesis_reaction.png&diff=1255 2019-01-27T22:02:30Z

<p>Herringi: Herringi uploaded a new version of File:Herringi alkyne synthesis reaction.png</p> <hr /> <div></div>

Herringi http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=File:Herringi_alkyne_synthesis_reaction.png&diff=1254 2019-01-27T22:00:27Z

<p>Herringi: </p> <hr /> <div></div>

Herringi