http://organicchem.sites.grinnell.edu/wiki/spring19/api.php?action=feedcontributions&feedformat=atom&user=Sharpest 2026-11-06T17:35:06Z User contributions MediaWiki 1.45.3 http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Amine&diff=1410 2019-05-03T18:28:49Z

<p>Sharpest: /* Gabriel Synthesis of Phenylalanine */</p> <hr /> <div>[[Main_Page]]<br /> __TOC__<br /> <br /> == Amine Synthesis (Dong Jin, Matthew, Park) ==<br /> <br /> [[File:Imine_to_amine_.png|1000px]]<br /> <br /> == Hoffmann rearrangement (Samuel Alves-Czachor) ==<br /> <br /> [[File:Swartz_wiki_rxn_1.png|1000px]]<br /> <br /> <br /> == Reductive Amination (Kyle Dixon-Anderson) ==<br /> <br /> The reductive amination of Benzaldehyde with Sodium cyanoborohydride and Aniline into N-benzylaniline<br /> <br /> [[File:Reductive.jpg]]<br /> <br /> == Synthesis of Aniline from benzene (Dong Jin Matthew park) ==<br /> <br /> [[File:Synthesis_of_aniline_from_benzene.png|1100px]]<br /> <br /> == Reduction of Nitrile to Amine using LiAlH4 (Cassie Staib) ==<br /> <br /> [[File:Reduction_of_nitrile_to_amine.png|900px]]<br /> <br /> == Amine with acid chloride, George Kaslow ==<br /> <br /> [[File:Amine_with_Acid_Chloride.png]]<br /> <br /> == Gabriel Synthesis of Phenylalanine- Steven Sharpe==<br /> <br /> [[File:Gsophan.PNG]]</div>

Sharpest http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Amine&diff=1409 2019-05-03T18:15:03Z

<p>Sharpest: </p> <hr /> <div>[[Main_Page]]<br /> __TOC__<br /> <br /> == Amine Synthesis (Dong Jin, Matthew, Park) ==<br /> <br /> [[File:Imine_to_amine_.png|1000px]]<br /> <br /> == Hoffmann rearrangement (Samuel Alves-Czachor) ==<br /> <br /> [[File:Swartz_wiki_rxn_1.png|1000px]]<br /> <br /> <br /> == Reductive Amination (Kyle Dixon-Anderson) ==<br /> <br /> The reductive amination of Benzaldehyde with Sodium cyanoborohydride and Aniline into N-benzylaniline<br /> <br /> [[File:Reductive.jpg]]<br /> <br /> == Synthesis of Aniline from benzene (Dong Jin Matthew park) ==<br /> <br /> [[File:Synthesis_of_aniline_from_benzene.png|1100px]]<br /> <br /> == Reduction of Nitrile to Amine using LiAlH4 (Cassie Staib) ==<br /> <br /> [[File:Reduction_of_nitrile_to_amine.png|900px]]<br /> <br /> == Amine with acid chloride, George Kaslow ==<br /> <br /> [[File:Amine_with_Acid_Chloride.png]]<br /> <br /> == Gabriel Synthesis of Phenylalanine ==<br /> <br /> [[File:Gsophan.PNG]]</div>

Sharpest http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=File:Gsophan.PNG&diff=1408 2019-05-03T18:14:48Z

<p>Sharpest: </p> <hr /> <div></div>

Sharpest http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Amine&diff=1407 2019-05-03T18:10:15Z

<p>Sharpest: /* Gabriel Synthesis of Phenylalanine */ new section</p> <hr /> <div>[[Main_Page]]<br /> __TOC__<br /> <br /> == Amine Synthesis (Dong Jin, Matthew, Park) ==<br /> <br /> [[File:Imine_to_amine_.png|1000px]]<br /> <br /> == Hoffmann rearrangement (Samuel Alves-Czachor) ==<br /> <br /> [[File:Swartz_wiki_rxn_1.png|1000px]]<br /> <br /> <br /> == Reductive Amination (Kyle Dixon-Anderson) ==<br /> <br /> The reductive amination of Benzaldehyde with Sodium cyanoborohydride and Aniline into N-benzylaniline<br /> <br /> [[File:Reductive.jpg]]<br /> <br /> == Synthesis of Aniline from benzene (Dong Jin Matthew park) ==<br /> <br /> [[File:Synthesis_of_aniline_from_benzene.png|1100px]]<br /> <br /> == Reduction of Nitrile to Amine using LiAlH4 (Cassie Staib) ==<br /> <br /> [[File:Reduction_of_nitrile_to_amine.png|900px]]<br /> <br /> == Amine with acid chloride, George Kaslow ==<br /> <br /> [[File:Amine_with_Acid_Chloride.png]]<br /> <br /> == Gabriel Synthesis of Phenylalanine ==<br /> <br /> [[File:Gabriel_Synthesis_of_Phenylalanine.png]]</div>

Sharpest http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=File:Gabriel_Synthesis_of_Phenylalanine.png&diff=1406 2019-05-03T18:08:29Z

<p>Sharpest: </p> <hr /> <div></div>

Sharpest http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Ketone&diff=1379 2019-03-13T13:31:15Z

<p>Sharpest: /* Jone&#039;s Oxidation-Steven Sharpe */ 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.</div>

Sharpest http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=File:Jone%27s_Oxidation.PNG&diff=1378 2019-03-13T13:26:51Z

<p>Sharpest: </p> <hr /> <div></div>

Sharpest http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Ether&diff=1277 2019-02-11T03:28:35Z

<p>Sharpest: </p> <hr /> <div>[[Main_Page]]<br /> __TOC__<br /> <br /> == Diethyl Ether (Matt Lieberman) ==<br /> <br /> Ethanol reacts with phosphorus tribromide to create ethyl bromide. Ethyl bromide can then react with more ethanol to create diethyl ether. Byproducts of the reaction are water and an increase of the acidity of the solution. [[File:Production of Ether.png|900px]]<br /> <br /> == Williamson Ether Synthesis (Alyssa Radakovich) ==<br /> <br /> A reaction of a methoxy group with butyl bromide forms methoxy butane. <br /> [[File:Wiki_Reaction_Collection1.png|1000px]]<br /> <br /> == Mitsunobu Reaction - Steven Sharpe ==<br /> <br /> Triphenylphosphine and DEAD react with the OH on the alcohol. The ETOH substitutes for the new compound, forming the ether.<br /> [[File:WIKI Reaction 1 - Mitsunobu.png|800px]]</div>

Sharpest http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Ether&diff=1274 2019-02-11T03:23:10Z

<p>Sharpest: </p> <hr /> <div>[[Main_Page]]<br /> __TOC__<br /> <br /> == Diethyl Ether (Matt Lieberman) ==<br /> <br /> Ethanol reacts with phosphorus tribromide to create ethyl bromide. Ethyl bromide can then react with more ethanol to create diethyl ether. Byproducts of the reaction are water and an increase of the acidity of the solution. [[File:Production of Ether.png|900px]]<br /> <br /> == Williamson Ether Synthesis (Alyssa Radakovich) ==<br /> <br /> A reaction of a methoxy group with butyl bromide forms methoxy butane. <br /> [[File:Wiki_Reaction_Collection1.png|1000px]]<br /> <br /> == Mitsunobu Reaction - Steven Sharpe ==<br /> <br /> [[File:WIKI Reaction 1 - Mitsunobu.png|800px]]</div>

Sharpest http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Alcohol&diff=1273 2019-02-11T03:22:50Z

<p>Sharpest: </p> <hr /> <div>[[Main_Page]]<br /> __TOC__<br /> <br /> == SN2 Epoxide Opening with Grignard Reagent - Anne Steensma == <br /> <br /> [[File:Sn2 epoxide to alcohol.png|800px]]<br /> <br /> == ethanal to 1-phenyl ethan-1-ol George Kaslow ==<br /> <br /> [[File:Untitled_Document-1.png]]<br /> <br /> == Primary Alcohol to Carboxylic Acid - Emily Mamrak ==<br /> <br /> [[File:Primary-alcohol-to-carboxylic-acid.png]]<br /> <br /> == Dihydroxylation of alkene - Klarie Li ==<br /> <br /> [[File:Dihydroxylation.png|600px]]</div>

Sharpest http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Alcohol&diff=1212 2019-01-23T16:25:45Z

<p>Sharpest: /* Mitsunobu Reaction - Steven Sharpe */ new section</p> <hr /> <div>[[Main_Page]]<br /> __TOC__<br /> <br /> == Mitsunobu Reaction - Steven Sharpe ==<br /> <br /> [[File:WIKI Reaction 1 - Mitsunobu.png|800px]]</div>

Sharpest http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=File:WIKI_Reaction_1_-_Mitsunobu.png&diff=1211 2019-01-23T16:22:04Z

<p>Sharpest: An example of the Mitsunobu Reaction, where the OH group is substituted by the OEt group.</p> <hr /> <div>An example of the Mitsunobu Reaction, where the OH group is substituted by the OEt group.</div>

Sharpest