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Boiling point (°C) K b (°C⋅kg/mol) Freezing point (°C) K f (°C⋅kg/mol) Data source; ... Acetic Anhydride: 139.0 [6] Ethylene Dichloride: 1.25 83.5 −35 [7 ...
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.
Acetic anhydride, or ethanoic anhydride, is the chemical compound with the formula (CH 3 CO) 2 O. Commonly abbreviated Ac 2 O , it is the simplest isolable anhydride of a carboxylic acid and is widely used as a reagent in organic synthesis .
Acetic acid can never be truly water-free in an atmosphere that contains water, so the presence of 0.1% water in glacial acetic acid lowers its melting point by 0.2 °C. [ 9 ] A common symbol for acetic acid is AcOH (or HOAc), where Ac is the pseudoelement symbol representing the acetyl group CH 3 −C(=O)− ; the conjugate base , acetate ( CH ...
Traditionally, acetaldehyde was mainly used as a precursor to acetic acid. This application has declined because acetic acid is produced more efficiently from methanol by the Monsanto and Cativa processes. Acetaldehyde is an important precursor to pyridine derivatives, pentaerythritol, and crotonaldehyde.
Melting point: 184 to 186 °C (363 to 367 °F; 457 to 459 K) ... In the laboratory, it can be easily synthesized from anthranilic acid and acetic anhydride.
Triple point: 289.8 K (16.7 °C), ? Pa Critical point: 593 K (320 °C), 57.8 bar Eutectic point with water –26.7 °C Std enthalpy change of fusionΔ fus H o +11.7 kJ/mol Std entropy change of fusionΔ fus S o: 40.5 J/(mol·K) Std enthalpy change of vaporizationΔ vap H o +23.7 kJ/mol Std entropy change of vaporizationΔ vap S o? J/(mol·K ...
Structure of the complex formed upon co-crystallization of pyromellitic anhydride (molecules terminated in red) and anthracene. [3] PMDA is an electron-acceptor, forming a variety of charge-transfer complexes. It reacts with amines to diimides, C 6 H 2 [(CO) 2 NR] 2 which also have acceptor properties. [4]