From Organic Chemistry Wiki Spring 2019
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| [[Main_Page]] | | [[Main_Page]] |
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| == CO2 to Carboxylic Acid (Lauren MacKenzie ==
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| 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.
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| [[File: CO2_to_Carboxylic_Acid.png|1100px]]
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| == Cyanonitrile to Carboxylic Acid (Kyra Neylan) ==
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| Reaction of propanonitrile in water with acid and heat to form propanoic acid and ammonium.
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| [[File: Cyanonitrile_to_Carboxylic_Acid_(Kyra_Neylan).png|1100px]]
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| == Chromium Trioxide to Carboxylic Acid (Noah Fluharty) ==
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| [[File:Chem_Wiki_1.png|1100px]]
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| == Ester Hydrolysis to Form Carboxylic Acid (Zhiye Lu) ==
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| Ester hydrolysis with acid catalysis to form carboxylic acid.
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| [[File:WIKI.png|1100px]]
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| == Aldehyde to Carboxylic Acid with Nitrile and Acid (Beth Ann Hansen) ==
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| [[File:Aldehyde_to_Carboxylic_Acid_with_Nitrile_and_Acid.png|1100px]]
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| == Decarboxylation of 1,3-dicarbonyl to form carboxylic acid (Zhiye Lu) ==
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| [[File:carboxylic acid.png|1100px]]
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| == Oxidative cleavage - conversion of alkynes to carboxylic acids (Daniel Hwang) ==
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| [[File:DHwang3.png|1100px]]
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Revision as of 18:30, 19 January 2018