Talk:Ketone: Difference between revisions
Jump to navigation
Jump to search
→Jone's Oxidation-Steven Sharpe: new section |
|||
| Line 25: | Line 25: | ||
[[File:Electrophilic_alkene_and_soft_nuclephile.png|600px]] | [[File:Electrophilic_alkene_and_soft_nuclephile.png|600px]] | ||
== Jone's Oxidation-Steven Sharpe == | |||
[[File:Jone's Oxidation.PNG]] | |||
The Jone's Oxidation provides an easy and relatively cheap way to oxidize an secondary alcohol into a ketone. When a primary alcohol is reduced, it forms a carboxylic acid. | |||
Revision as of 13:31, 13 March 2019
Synthesis of a Ketone from an Acyl Chloride using a Gilman reagent (Nichole Hannan)
Synthesis of ketone from a secondary alcohol (Chloe Wu)
Acetic Anhydride and a Grignard Reagent react with an acid workup to produce Acetic Acid and Acetophenone (Malia Wells)
Synthesis of ketone from a secondary alcohol (Emily Mamrak)
Synthesis of 2-butanone from 1-butyne (Madison Howe)
Electrophilic alkene and soft nucleophile - Klarie Li
Jone's Oxidation-Steven Sharpe
The Jone's Oxidation provides an easy and relatively cheap way to oxidize an secondary alcohol into a ketone. When a primary alcohol is reduced, it forms a carboxylic acid.