Talk:Ketone: Difference between revisions
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→Nucleophilic Addition to Alkyne (Lauren MacKenzie: new section |
→Dimethyl ketone by ozonolysis (Kyra Neylan): new section |
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The product easily transforms between the keto and enol forms (hence the double arrows), but the keto form is predominant. | 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]] | |||
Revision as of 02:10, 17 February 2017
Hydrolysis to from Acetone
Heather RoeschFile:Ketone (Acetone).png
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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
