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A variety of organic reactions employ acetone as a polar, aprotic solvent, e.g. the Jones oxidation. Because acetone is cheap, volatile, and dissolves or decomposes with most laboratory chemicals, an acetone rinse is the standard technique to remove solid residues from laboratory glassware before a final wash. [66]
Liquid properties Std enthalpy change of formation, Δ f H o liquid: −249.4 kJ/mol Standard molar entropy, S o liquid: 200.4 J/(mol K) Enthalpy of combustion, Δ c H o –1785.7 kJ/mol Heat capacity, c p: 125.5 J/(mol K) Gas properties Std enthalpy change of formation, Δ f H o gas: −218.5 kJ/mol Standard molar entropy, S o gas: 295.35 J ...
Solvent Density (g cm-3) Boiling point (°C) K b (°C⋅kg/mol) ... Acetone: 0.78 56.2 1.67 –94.8 K b [3] Benzene: 0.87 80.1 2.65 5.5 –5.12 K b & K f [2 ...
Specific uses for organic solvents are in dry cleaning (e.g. tetrachloroethylene); as paint thinners (toluene, turpentine); as nail polish removers and solvents of glue (acetone, methyl acetate, ethyl acetate); in spot removers (hexane, petrol ether); in detergents (citrus terpenes); and in perfumes .
This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.
Acetone, commonly found as a fraction of nail polish remover (or at hardware stores in pure form), is a widely available solvent capable of softening cured cyanoacrylate. [36] Other solvents include nitromethane, dimethylformamide, [37] dimethyl sulfoxide, and methylene chloride. [38]
The simplest ketone is acetone (where R and R' is methyl), with the formula (CH 3) 2 CO. Many ketones are of great importance in biology and industry. Examples include many sugars , many steroids (e.g., testosterone), and the solvent acetone. [1]
The equilibrium constant tends to be high in nonpolar solvents; when K keto→enol is equal or greater than 1, the enol form is favoured. The keto form becomes more favourable in polar, hydrogen-bonding solvents, such as water. [7] The enol form is a vinylogous analogue of a carboxylic acid. [citation needed]
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