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A concentrated solution of sodium bicarbonate is added to the reaction mixture. This will promote the migration of impurities and byproducts to the aqueous layer and leave the product in the dichloromethane (organic layer). The aqueous and organic layers are allowed to separate. This process is typically performed in a separatory funnel.
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
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.
Buffers typically consist of a pair of compounds in solution, one of which is a weak acid and the other a weak base. [13] The most abundant buffer in the ECF consists of a solution of carbonic acid (H 2 CO 3), and the bicarbonate (HCO − 3) salt of, usually, sodium (Na +). [5] Thus, when there is an excess of OH −
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.
The self-ionization of water (also autoionization of water, autoprotolysis of water, autodissociation of water, or simply dissociation of water) is an ionization reaction in pure water or in an aqueous solution, in which a water molecule, H 2 O, deprotonates (loses the nucleus of one of its hydrogen atoms) to become a hydroxide ion, OH −.
Solutions of metal aquo complexes are acidic owing to the ionization of protons from the water ligands. In dilute solution chromium(III) aquo complex has a pK a of about 4.3: [Cr(H 2 O) 6] 3+ ⇌ [Cr(H 2 O) 5 (OH)] 2+ + H + Thus, the aquo ion is a weak acid, of comparable strength to acetic acid (pK a of about 4.8). This pK a is typical of the ...
Acid catalysis is mainly used for organic chemical reactions. Many acids can function as sources for the protons. Acid used for acid catalysis include hydrofluoric acid (in the alkylation process), phosphoric acid, toluenesulfonic acid, polystyrene sulfonate, heteropoly acids, zeolites.