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Resorcinol (or resorcin) is a phenolic compound. It is an organic compound with the formula C 6 H 4 (OH) 2. It is one of three isomeric benzenediols, the 1,3-isomer (or meta-isomer). Resorcinol crystallizes from benzene as colorless needles that are readily soluble in water, alcohol, and ether, but insoluble in chloroform and carbon disulfide. [6]
Hydroquinone, also known as benzene-1,4-diol or quinol; Resorcinol This page was last edited on 28 August 2022, at 12:44 (UTC ...
There are three structural isomers: 1,2-dihydroxybenzene (the ortho isomer) is commonly known as catechol, 1,3-dihydroxybenzene (the meta isomer) is commonly known as resorcinol, and 1,4-dihydroxybenzene (the para isomer) is commonly known as hydroquinone. [1]
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1,3-Cyclohexanedione is produced by semi-hydrogenation of resorcinol: [3] [4] C 6 H 4 (OH) 2 + H 2 → C 6 H 8 O 2. 1,3-Cyclohexanedione exists in solution predominantly as the enol tautomer. Enolization of 1,3-cyclohexanedione.
Density: 1.3756 g/mL ... (trichloromethyl)benzene, is an organic compound with the formula C 6 H 5 CCl 3. ... C 6 H 5 CCl 3 + resorcinol → 2,4-dihydroxybenzophenone ...
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.
3-Aminophenol can be prepared by caustic fusion of 3-aminobenzenesulfonic acid (i.e. heating with NaOH to 245 °C for 6 hours) [4] or from resorcinol via a substitution reaction with ammonium hydroxide. [5]