|
|
| Line 1: |
Line 1: |
| [[Main_Page]] | | [[Main_Page]] |
| __TOC__ | | __TOC__ |
|
| |
| == Hydrolysis to from Acetone ==
| |
|
| |
| Heather Roesch[[File:Ketone (Acetone).png]]
| |
|
| |
| == Rachel Tappe: Oxidation of an alcohol into a ketone ==
| |
|
| |
| [[File:Screenshot_2017-01-28_15.16.43.png|1100px]]
| |
|
| |
| == Frieden Crafts Acylation (Katie McDonald) ==
| |
|
| |
| [[File:Friedel_Crafts_Acylation.png|1100px]]
| |
|
| |
| == Nucleophilic Addition to Alkyne (Lauren MacKenzie ==
| |
|
| |
| [[File:Rxn_2.png|1100px]]
| |
|
| |
| 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|900px]]
| |
|
| |
| == The Clemmensen Reduction Rong Guo==
| |
|
| |
| [[File:The Clemmensen Reduction Rong Guo.png|500px]]
| |
|
| |
| == Acetal Formation (Ky-Sean Johnson) ==
| |
|
| |
| [[File:AcetalJohnson.png|1100px]]
| |
|
| |
| == Heterocycle ketone addition (Lila Cardozo) ==
| |
|
| |
| [[File:Wiki4_heterocycles.png|1100px]]
| |
|
| |
| == Michael Condensation (Liangchen Liu) ==
| |
|
| |
| [[File:Wiki4.png|1100px]]
| |
|
| |
| == Swern Oxidation of Primary Alcohol (Noah Fluharty) ==
| |
|
| |
| [[File:Reaction_4.png|1100px]]
| |
|
| |
| == Decarboxylation of 1,3-dicarbonyl to form ketone (Zhiye Lu) ==
| |
|
| |
| [[File:ketone.png|1100px]]
| |
|
| |
| == Aldol_Condensation Shudi Pan ==
| |
|
| |
| [[File:Aldol_Condensation.png|1100x]]
| |
|
| |
| == alpha,beta unsaturated ketone alkene reduction (Katie McDonald) ==
| |
|
| |
| [[File:Ketone1.png|1100px]]
| |