Talk:Ketone: Difference between revisions
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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. | 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. | ||
== synthesis of 4-(4-methoxyphenyl)-3-Buten-2-one from 4-methoxy-benzaldehyde and acetone from aldol addition - ( Xuanhe Chen ) == | |||
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Revision as of 03:52, 15 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.
synthesis of 4-(4-methoxyphenyl)-3-Buten-2-one from 4-methoxy-benzaldehyde and acetone from aldol addition - ( Xuanhe Chen )
