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The conversion of methyl acetate back into its components, by an acid, is a first-order reaction with respect to the ester. The reaction of methyl acetate and a base, for example sodium hydroxide, is a second-order reaction with respect to both reactants. Methyl acetate is a Lewis base that forms 1:1 adducts with a variety of Lewis acids.
Methyl acetate is used in place of methanol as a source of methyl iodide. [5] CH 3 CO 2 CH 3 + CO → (CH 3 CO) 2 O. In this process lithium iodide converts methyl acetate to lithium acetate and methyl iodide, which in turn affords, through carbonylation, acetyl iodide. Acetyl iodide reacts with acetate salts or acetic acid to give the anhydride.
Copper naphthenate is commonly prepared by treatment of naphthenic acid with copper (II) compounds such as basic copper carbonate or copper hydroxide. [1] Even copper (II) sulfate can be treated with sodium or potassium naphthenate in aqueous solutions. The reaction of copper metal with naphthenic acid, which has been used commercially ...
Transesterification is the process of exchanging the organic functional group R″ of an ester with the organic group R' of an alcohol. These reactions are often catalyzed by the addition of an acid or base catalyst. [1] Strong acids catalyze the reaction by donating a proton to the carbonyl group, thus making it a more potent electrophile.
Hydrolysis of methyl formate gives formic acid and regenerates methanol: HCOOCH 3 → HCOOH + CH 3 OH. Formic acid is used for many applications in industry. Formate esters often are fragrant or have distinctive odors. Compared to the more common acetate esters, formate esters are less commonly used commercially because they are less stable. [5]
Infobox references. Propylene glycol methyl ether acetate (PGMEA, 1-methoxy-2-propanol acetate) is a P-type glycol ether used in inks, coatings, and cleaners. It is sold by Dow Chemical under the name Dowanol PMA, [3] by Shell Chemical under the name methyl proxitol acetate, [4][5] and by Eastman under the name PM Acetate. [6]
Biodiesel production is the process of producing the biofuel, biodiesel, through the chemical reactions of transesterification and esterification. [1] This process renders a product (chemistry) and by-products. The fats and oils react with short-chain alcohols (typically methanol or ethanol). The alcohols used should be of low molecular weight.
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 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.