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Acetophenone is formed as a byproduct of the cumene process, the industrial route for the synthesis of phenol and acetone.In the Hock rearrangement of isopropylbenzene hydroperoxide, migration of a methyl group rather than the phenyl group gives acetophenone and methanol as a result of an alternate rearrangement of the intermediate:
This Wikipedia page provides a comprehensive list of boiling and freezing points for various solvents.
Standard molar entropy, S o solid? J/(mol K) Heat capacity, c p [2] 96 J/(mol K) 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 ...
The molecular formula C 8 H 8 O (molar mass: 120.15 g/mol, exact mass: 120.057515 u) may refer to: Acetophenone; Methylbenzaldehydes. 2-Methylbenzaldehyde; 3-Methylbenzaldehyde; 4-Methylbenzaldehyde; Oxonine; Phenylacetaldehyde; Phthalane; Styrene oxide; 4-Vinylphenol
Acetone (2-propanone or dimethyl ketone) is an organic compound with the formula (CH 3) 2 CO. [22] It is the simplest and smallest ketone (R−C(=O)−R').It is a colorless, highly volatile, and flammable liquid with a characteristic pungent odour, very reminiscent of the smell of pear drops.
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Molar mass: 199.047 g·mol −1 Appearance Colorless solid Melting point: 50 °C (122 °F; 323 K) [1] Boiling point: 136 °C (277 °F; 409 K) 18 mm Hg [1] Hazards Occupational safety and health (OHS/OSH):
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