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2-Naphthalenethiol is an organosulfur compound with the formula C 10 H 7 SH. It is a white solid. It is a white solid. It is one of two mono thiols of naphthalene , the other being 1-naphthalenethiol .
2-Naphthalenethiol This page was last edited on 13 November 2022, at 22:54 (UTC). Text is available under the Creative Commons Attribution-ShareAlike 4.0 License ...
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Traditionally, 2-naphthol is produced by a two-step process that begins with the sulfonation of naphthalene in sulfuric acid: [2] C 10 H 8 + H 2 SO 4 → C 10 H 7 SO 3 H + H 2 O. The sulfonic acid group is then cleaved in molten sodium hydroxide: C 10 H 7 (SO 3 H) + 3 NaOH → C 10 H 7 ONa + Na 2 SO 3 + 2 H 2 O. Neutralization of the product ...
ClCH 2 CO 2 H + Na 2 S 2 O 3 → Na[O 3 S 2 CH 2 CO 2 H] + NaCl Na[O 3 S 2 CH 2 CO 2 H] + H 2 O → HSCH 2 CO 2 H + NaHSO 4. Organolithium compounds and Grignard reagents react with sulfur to give the thiolates, which are readily hydrolyzed: [27] RLi + S → RSLi RSLi + HCl → RSH + LiCl. Phenols can be converted to the thiophenols via ...
Naphtha (/ ˈ n æ f θ ə /, recorded as less common or nonstandard [1] in all dictionaries: / ˈ n æ p θ ə /) is a flammable liquid hydrocarbon mixture.Generally, it is a fraction of crude oil, but it can also be produced from natural-gas condensates, petroleum distillates, and the fractional distillation of coal tar and peat.
2-Naphthylamine or 2-aminonaphthalene is one of two isomeric aminonaphthalenes, compounds with the formula C 10 H 7 NH 2. It is a colorless solid, but samples take on a reddish color in air because of oxidation. It was formerly used to make azo dyes, but it is a known carcinogen and has largely been replaced by less toxic compounds. [2]
2-Naphthoic acid is an organic compound of the formula C 10 H 7 CO 2 H. It is one of two isomeric carboxylic acid derivatives of naphthalene , the other one being 1-naphthoic acid . It can be prepared by carboxylation of 1-chloronaphthalene .