Talk:Ketone: Difference between revisions
Jump to navigation
Jump to search
→Acetal Formation (Ky-Sean Johnson): new section |
→Heterocycle ketone addition (Lila Cardozo): new section |
||
| Line 32: | Line 32: | ||
[[File:AcetalJohnson.png|1100px]] | [[File:AcetalJohnson.png|1100px]] | ||
== Heterocycle ketone addition (Lila Cardozo) == | |||
[[File:Wiki4_heterocycles.png|1100px]] | |||
Revision as of 03:41, 9 May 2017
Hydrolysis to from Acetone
Heather Roesch.png)
Rachel Tappe: Oxidation of an alcohol into a ketone
Frieden Crafts Acylation (Katie McDonald)
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).
The Clemmensen Reduction Rong Guo
Acetal Formation (Ky-Sean Johnson)
Heterocycle ketone addition (Lila Cardozo)
