Talk:Ketone: Difference between revisions
Jump to navigation
Jump to search
→Heterocycle ketone addition (Lila Cardozo): new section |
→Michael Condensation (Liangchen Liu): new section |
||
| Line 36: | Line 36: | ||
[[File:Wiki4_heterocycles.png|1100px]] | [[File:Wiki4_heterocycles.png|1100px]] | ||
== Michael Condensation (Liangchen Liu) == | |||
[[File:Wiki4.png|1100px]] | |||
Revision as of 19:57, 9 May 2017
Hydrolysis to from Acetone
Heather RoeschFile:Ketone (Acetone).png
Rachel Tappe: Oxidation of an alcohol into a ketone
File:Screenshot 2017-01-28 15.16.43.png
Frieden Crafts Acylation (Katie McDonald)
File:Friedel Crafts Acylation.png
Nucleophilic Addition to Alkyne (Lauren MacKenzie
The product easily transforms between the keto and enol forms (hence the double arrows), but the keto form is predominant.
Dimethyl ketone by ozonolysis (Kyra Neylan)
2,3-dimethylbut-2-ene reacts with ozone and then dimethyl sulfide to form dimethylketone (acetone). File:Ozonolysis.png
The Clemmensen Reduction Rong Guo
File:The Clemmensen Reduction Rong Guo.png