Talk:Alkene: Difference between revisions

From Organic Chemistry Wiki Spring 2018
Jump to navigation Jump to search
Petersos (talk | contribs)
Removing previous entries; add TOC.
 
Hewittmi (talk | contribs)
 
(21 intermediate revisions by 14 users not shown)
Line 1: Line 1:
[[Main_Page]]
[[Main_Page]]
__TOC__
__TOC__
== Wittig Reaction (Matthew Palmeri) ==
[[File:Wiki Entry 1.png|1000px]]
== Halogenated hydrocarbon elimination (Suze Jiang) ==
[[File:1.png|1100px]]
== Ketone to Alkene: Formation of N,_N,_1-trimethylethenamine (Yuwei Pan) ==
[[File:N,_N,_1-trimethylethenamine.png|600px]]
== Crossed Aldol (Christine Solomon) ==
[[File:WikiRxnCrossedAldolAlkene.png|800px]]
== Hydrogenation of an Alkyne to an Alkene (Madison Wardlaw) ==
[[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.
== 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

Main_Page

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