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In this example the organic layer is the product, which is a liquid at room temperature. The bottom aqueous layer is removed with a pipette and discarded. The top layer is transferred to an Erlenmeyer flask where it is treated with anhydrous sodium sulfate to remove any remaining water.
The mechanism of the reaction involves two steps. The first step is a nucleophilic addition to the nitrile with the aid of a polarizing Lewis acid, forming an imine, which is later hydrolyzed during the aqueous workup to yield the final aryl ketone. Hoesch reaction mechanism
The complex is destroyed upon aqueous workup to give the desired ketone. For example, the classical synthesis of deoxybenzoin calls for 1.1 equivalents of AlCl 3 with respect to the limiting reagent, phenylacetyl chloride. [14]
The resulting hydroquinone is poorly soluble in typical reaction solvents (dioxane, benzene, alkanes), which facilitates workup. Solutions of DDQ in benzene are red, due to the formation of a charge-transfer complex. [9]
Acid–base extraction is a subclass of liquid–liquid extractions and involves the separation of chemical species from other acidic or basic compounds. [1] It is typically performed during the work-up step following a chemical synthesis to purify crude compounds [2] and results in the product being largely free of acidic or basic impurities.
The McMurry reaction of benzophenone. The McMurry reaction is an organic reaction in which two ketone or aldehyde groups are coupled to form an alkene using a titanium chloride compound such as titanium(III) chloride and a reducing agent.
Get ready for all of today's NYT 'Connections’ hints and answers for #549 on Wednesday, December 11, 2024. Today's NYT Connections puzzle for Wednesday, December 11, 2024The New York Times.
This mechanism is today considered the actual mechanism taking place in olefin metathesis. Chauvin's experimental evidence was based on the reaction of cyclopentene and 2-pentene with the homogeneous catalyst tungsten(VI) oxytetrachloride and tetrabutyltin: The three principal products C9, C10 and C11 are found in a 1:2:1 regardless of conversion.