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1-Naphthol, or α-naphthol, is an organic compound with the formula C 10 H 7 OH. It is a fluorescent white solid. 1-Naphthol differs from its isomer 2-naphthol by the location of the hydroxyl group on the naphthalene ring. The naphthols are naphthalene homologues of phenol. Both isomers are soluble in simple organic solvents. They are ...
Boiling point (°C) K b (°C⋅kg/mol) Freezing point (°C) K f (°C⋅kg/mol) Data source; Aniline: 184.3 3.69 –5.96 –5.87 K b & K f [1] Lauric acid: 298.9 44 –3.9 Acetic acid: 1.04 117.9 3.14 16.6 –3.90 K b [1] K f [2] 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] Bromobenzene: 1.49 156.0 6. ...
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.
c 10 h 8 + 4.5 o 2 → c 6 h 4 (co) 2 o + 2 co 2 + 2 h 2 o This reaction is the basis of the main use of naphthalene. Oxidation can also be effected using conventional stoichiometric chromate or permanganate reagents.
2-Naphthol, or β-naphthol, is a fluorescent colorless (or occasionally yellow) crystalline solid with the formula C 10 H 7 OH. It is an isomer of 1-naphthol , differing by the location of the hydroxyl group on the naphthalene ring.
This page was last edited on 14 November 2024, at 15:02 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.
Naphthol may refer to: 1-Naphthol; 2-Naphthol This page was last edited on 26 June 2023, at 00:21 (UTC). Text is available under the Creative Commons Attribution ...
1-Nitroso-2-naphthol can be prepared by treatment of 2-naphthol with nitrous acid: [3] C 10 H 7 OH + HNO 2 → C 10 H 6 (NO)OH + H 2 O. Its conjugate base forms deeply colored complexes with iron(II) and cobalt(II), complexes [M(C 10 H 6 (NO)O) 3] 2-. [4] The deep colors of these complexes results from the delocalized bonding within each five ...