From Organic Chemistry Wiki Spring 2019
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| == Nitrile (Hannah Hong) ==
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| A reaction of an amide with thionyl chloride to form a nitrile.
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| [[File:Nitrile.png|1100px]]
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| == Hydrolysis of Nitrile ==
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| A process of Nitrile hydrolysis (Two H2O attacks) that generates carboxylic acid with no change to the carbon chain.
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| [[File:Hydrolysis_of_nitrile.png]]
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| == Creating a Nitrile using an amide and phosphorus(V) oxide (Guzman, Iridian) ==
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| [[File:Making Nitriles from amides.png|1100px]]
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| == Jennings_4th pass_Synthesis of 2-(1H-indol-3-yl)acetonitrile via NaCN and 3-(chloromethyl)-1H-indole ==
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| [[File:Acetonitrile.png]]
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| == Nitrile reduced to aldehyde using diisobutylaluminum hydride (Alfredo) ==
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| [[File:Nitrile_Thingy.png|1100px]]
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| == Reduction of Cyano Group (Jordan Hamilton) ==
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| [[File:4.jpg]]
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Revision as of 18:31, 19 January 2018