Talk:Alkene: Difference between revisions
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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. | 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) == | |||
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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)
Crossed Aldol (Christine Solomon)
Hydrogenation of an Alkyne to an Alkene (Madison Wardlaw)
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)
