Talk:Alkene: Difference between revisions
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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]] | |||
== Dehydration of Alcohol (Yeaseul Kim) == | |||
[[File: Dehydration_of_Primary_Alcohol.png|1100px]] | |||
== Aldol Condensation Bretta McCall[[File:Aldolcondsn.png]] == | |||
Cyclic aldol condensation | |||
== Michael Hewitt Lindlar Reduction == | |||
[[File:Screen Shot 2018-05-15 at 7.37.18 AM.png]] | |||
Latest revision as of 12:39, 15 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)
Dehydration of Alcohol (Yeaseul Kim)
Aldol Condensation Bretta McCall
Cyclic aldol condensation
Michael Hewitt Lindlar Reduction
