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The reaction is named after Russian organic chemist Vyacheslav Tishchenko, who discovered that aluminium alkoxides are effective catalysts for the reaction. [1] [2] [3] In the related Cannizzaro reaction, the base is sodium hydroxide and then the oxidation product is a carboxylic acid and the reduction product is an alcohol.
Ethyl acetate (systematically ethyl ethanoate, commonly abbreviated EtOAc, ETAC or EA) is the organic compound with the formula CH 3 CO 2 CH 2 CH 3, simplified to C 4 H 8 O 2.This flammable, colorless liquid has a characteristic sweet smell (similar to pear drops) and is used in glues, nail polish removers, and the decaffeination process of tea and coffee.
Typically aqueous sodium hydroxide solutions are used. [1] [2] It is an important type of alkaline hydrolysis. When the carboxylate is long chain, its salt is called a soap. The saponification of ethyl acetate gives sodium acetate and ethanol: C 2 H 5 O 2 CCH 3 + NaOH → C 2 H 5 OH + NaO 2 CCH 3
Aluminium acetate or aluminium ethanoate [1] (also "aluminum ~"), sometimes abbreviated AlAc in geochemistry, [2] can refer to a number of different salts of aluminium with acetic acid. In the solid state, three salts exist under this name: basic aluminium monoacetate , (HO) 2 AlCH 3 CO 2 , basic aluminium diacetate , HOAl(CH 3 CO 2 ) 2 , [ 3 ...
Sodium hydroxide, also known as lye and caustic soda, [1] [2] is an inorganic compound with the formula NaOH. It is a white solid ionic compound consisting of sodium cations Na + and hydroxide anions OH −. Sodium hydroxide is a highly corrosive base and alkali that decomposes lipids and proteins at ambient temperatures and may cause severe ...
An allylic diazene rearrangement was used in the synthesis of the C 21 –C 34 fragment of antascomicin B. [43] The hydrazone was reduced selectively with catecholborane and excess reducing agent decomposed with sodium thiosulfate. The crude reaction product was then treated with sodium acetate and to give the 1,4-syn isomer. Scheme 22.
In hot concentrated hydrochloric acid, aluminium reacts with water with evolution of hydrogen, and in aqueous sodium hydroxide or potassium hydroxide at room temperature to form aluminates—protective passivation under these conditions is negligible. [9] The reaction with aqueous alkali is often written: [2] Al + NaOH + H 2 O → NaAlO 2 ...
The S N 2 reaction between sodium acetate and bromoethane. The products are ethyl acetate and sodium bromide. The nucleophilicity of carboxylate ions is much weaker than that of hydroxide and alkoxide ions, but stronger than that of halide anions (in a polar aprotic solvent, though there are other effects such as solubility of the ion).