From Organic Chemistry Wiki Spring 2019
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| [[Main_Page]] | | [[Main_Page]] |
| __TOC__ | | __TOC__ |
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| == Wittig Reaction (Matthew Palmeri) ==
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| [[File:Wiki Entry 1.png|1000px]]
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| == Halogenated hydrocarbon elimination (Suze Jiang) ==
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| [[File:1.png|1100px]]
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| == Ketone to Alkene: Formation of N,_N,_1-trimethylethenamine (Yuwei Pan) ==
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| [[File:N,_N,_1-trimethylethenamine.png|600px]]
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| == Crossed Aldol (Christine Solomon) ==
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| [[File:WikiRxnCrossedAldolAlkene.png|800px]]
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| == Hydrogenation of an Alkyne to an Alkene (Madison Wardlaw) ==
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| [[File:Wiki_assignment_4.png|825px]]
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| Using a hydrogen-palladium catalyst in the presence of quinoline reduces the alkyne to an alkene and forms a cis product.
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| == Diels-Alder Reaction (Ed Lopatto) ==
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| [[File:DielsAlder_Wiki_Lopatto.png|500px]]
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| == Dehydration of Alcohol (Yeaseul Kim) ==
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| [[File: Dehydration_of_Primary_Alcohol.png|1100px]]
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| == Aldol Condensation Bretta McCall[[File:Aldolcondsn.png]] ==
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| Cyclic aldol condensation
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| == Michael Hewitt Lindlar Reduction ==
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| [[File:Screen Shot 2018-05-15 at 7.37.18 AM.png]]
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Revision as of 18:57, 17 January 2019