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Boiling point (°C) K b (°C⋅kg/mol) Freezing point (°C) K f (°C⋅kg/mol) Data source; Aniline: 184.3 ... Phenol: 181.75 3.60 43.0 –7.27 K f [2] K b [1] Water ...
Boiling point: 181.7 °C (359.1 °F; 454.8 K) ... Phenol is more acidic than aliphatic alcohols. ... phenol hydrogen bonds with a wide range of Lewis bases such as ...
In chemistry, an alcohol (from Arabic al-kuḥl 'the kohl'), [2] is a type of organic compound that carries at least one hydroxyl (−OH) functional group bound to a saturated carbon atom. [3] [4] Alcohols range from the simple, like methanol and ethanol, to complex, like sugars and cholesterol. The presence of an OH group strongly modifies the ...
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.
Phenol is readily alkylated at the ortho positions using alkenes in the presence of a Lewis acid such as aluminium phenoxide: [citation needed] CH 2 =CR 2 + C 6 H 5 OH → R 2 CHCH 2 -2-C 6 H 4 OH More than 100,000 tons of tert-butyl phenols are produced annually (year: 2000) in this way, using isobutylene (CH 2 =CMe 2 ) as the alkylating agent.
At atmospheric pressure, mixtures of ethanol and water form an azeotrope at about 89.4 mol% ethanol (95.6% ethanol by mass, [84] 97% alcohol by volume), with a boiling point of 351.3 K (78.1 °C). [85] At lower pressure, the composition of the ethanol-water azeotrope shifts to more ethanol-rich mixtures. [86]
Boiling point: 191.0 °C (464.2 K) ... The name "cresol" is an adduct of phenol and their ... Another isomer of cresol is called Benzyl alcohol, or alpha ...
This process coforms cyclohexanone, and this mixture ("KA oil" for ketone-alcohol oil) is the main feedstock for the production of adipic acid. The oxidation involves radicals and the intermediacy of the hydroperoxide C 6 H 11 O 2 H. Alternatively, cyclohexanol can be produced by the hydrogenation of phenol: C 6 H 5 OH + 3 H 2 → C 6 H 11 OH