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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.
−480 kJ/mol Standard molar entropy, S o liquid: 259.4 J/(mol K) Heat capacity, c p: 170 J/(mol K) Gas properties Std enthalpy change of formation, Δ f H o gas: −445 kJ/mol Standard molar entropy, S o gas: 363 J/(mol K) Heat capacity, c p: 125.8 J/(mol K) (360 K) van der Waals' constants [2] a = 2072.0 L 2 kPa/mol 2 b = 0.1412 liter per mole
In chemistry, the molar mass (M) (sometimes called molecular weight or formula weight, but see related quantities for usage) of a chemical compound is defined as the ratio between the mass and the amount of substance (measured in moles) of any sample of the compound. [1] The molar mass is a bulk, not molecular, property of a substance.
For example, acetic acid and ethanol gives ethyl acetate and water. CH 3 COO−H + HO−CH 2 CH 3 → CH 3 COO−CH 2 CH 3 + H 2 O. Most acetate esters, however, are produced from acetaldehyde using the Tishchenko reaction. In addition, ether acetates are used as solvents for nitrocellulose, acrylic lacquers, varnish removers, and wood stains.
The molar amount of the reactants is calculated from the weights (acetic acid: 120 g ÷ 60 g/mol = 2.0 mol; ethanol: 230 g ÷ 46 g/mol = 5.0 mol). Ethanol is used in a 2.5-fold excess (5.0 mol ÷ 2.0 mol). The theoretical molar yield is 2.0 mol (the molar amount of the limiting compound, acetic acid). The molar yield of the product is ...
Equivalent weights may be calculated from molar masses if the chemistry of the substance is well known: sulfuric acid has a molar mass of 98.078(5) g mol −1, and supplies two moles of hydrogen ions per mole of sulfuric acid, so its equivalent weight is 98.078(5) g mol −1 /2 eq mol −1 = 49.039(3) g eq −1.
The enzyme acetylacetone dioxygenase cleaves a central carbon-carbon bond of acetylacetone, producing acetate and 2-oxopropanal. The enzyme is iron(II)-dependent, but it has been proven to bind to zinc as well. Acetylacetone degradation has been characterized in the bacterium Acinetobacter johnsonii. [13] CH 3 C(O)CH 2 C(O)CH 3 + O 2 → CH 3 ...
Molar mass: 84.93 g·mol −1 ... Miscible in ethyl acetate, alcohol ... Although DCM is a common solvent in organic chemistry laboratories and is ...