Talk:Ketone: Difference between revisions
Jump to navigation
Jump to search
No edit summary |
|||
| (4 intermediate revisions by 3 users not shown) | |||
| Line 36: | Line 36: | ||
[[File:Step2-1.jpg|1000px]] | [[File:Step2-1.jpg|1000px]] | ||
== Synthesis of | == Synthesis of 1-(p-tolyl)propan-2-one from 1-bromo-4-methylbenzene using Potassium 2-oxopropan-1-ide (Kyle Dixon-Anderson) == | ||
[[File:Aromatic+ketone synthesis.jpg]] | [[File:Aromatic+ketone synthesis.jpg]] | ||
== Synthesis of Ketone by Fredyl-Craft Acylation (Amelia Zoernig) == | |||
[[File:Fcaketone.JPG]] | |||
== Converting ester to ketone (Isaias Herring) == | |||
[[File:Converting_ester_to_ketone.PNG|1100px]] | |||
Latest revision as of 21:25, 10 May 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 )
Synthesis of 1-(p-tolyl)propan-2-one from 1-bromo-4-methylbenzene using Potassium 2-oxopropan-1-ide (Kyle Dixon-Anderson)
Synthesis of Ketone by Fredyl-Craft Acylation (Amelia Zoernig)
Converting ester to ketone (Isaias Herring)
