Talk:Alkene: Difference between revisions
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→Diels-Alder Reaction (Ed Lopatto): new section |
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[[File:Wiki_assignment_4.png|825px]] | [[File:Wiki_assignment_4.png|825px]] | ||
Using a hydrogen-palladium catalyst in the presence of quinoline reduces the alkyne to an alkene and forms a cis product. | Using a hydrogen-palladium catalyst in the presence of quinoline reduces the alkyne to an alkene and forms a cis product. | ||
== Diels-Alder Reaction (Ed Lopatto) == | |||
[[File:DielsAlder_Wiki_Lopatto.png|500px]] | |||
Revision as of 03:44, 8 May 2018
Wittig Reaction (Matthew Palmeri)
Halogenated hydrocarbon elimination (Suze Jiang)
Ketone to Alkene: Formation of N,_N,_1-trimethylethenamine (Yuwei Pan)
File:N, N, 1-trimethylethenamine.png
Crossed Aldol (Christine Solomon)
File:WikiRxnCrossedAldolAlkene.png
Hydrogenation of an Alkyne to an Alkene (Madison Wardlaw)
File:Wiki assignment 4.png Using a hydrogen-palladium catalyst in the presence of quinoline reduces the alkyne to an alkene and forms a cis product.
