... sometimes called phenols, consist of an aromatic 6-carbon ring bonded to a hydroxy group. Some phenols have antiseptic ... "Phenols". Plant Defense Systems & Medicinal Botany. Retrieved 2007-05-21. Van Soest, Peter J. (1982). Nutritional ecology of ...
... phenols, hydrocarbons • and polycyclic aromatic hydrocarbons • other acute and chronic toxicants In many cases, huge ponds sit ...
2004). The Chemistry of Phenols. Chichester: John Wiley & Sons. ISBN 9780470869451. Sharma, Vinita; McKone, Harold T.; Markow, ...
Tyman, J.H.P. (1996). Synthetic and Natural Phenols. Burlington: Elsevier. ISBN 0-08-054219-0. ed.-in-chief, George M. Garrity ...
Curtis, R. F.; Hassall, C. H.; Nazar, M. (1968). "The biosynthesis of phenols. Part XV. Some metabolites of Penicillium ...
Kharasch, M. S.; Joshi, B. S. (1957). "Reactions of Hindered Phenols. II. Base-Catalyzed Oxidations of Hindered Phenols". J. Am ... It may be synthesized by oxidation of the parent phenol with lead dioxide or potassium hexacyanoferrate(III). Its radical ...
"Phenols and Related Compounds". The Merck Veterinary Manual. Merck Manuals. Retrieved 16 April 2015. "Pineda Ejected for Pine ...
... is prepared from phenol and chloroform by heating with sodium hydroxide or potassium hydroxide in a Reimer- ... Salicylaldehydes in general may be prepared from the corresponding phenol by the Duff reaction, or by treatment with ... "Ortho-Formylation of Phenols; Preparation of 3-Bromosalicylaldehyde". Organic Syntheses. 82: 64. Janeš, D.; Kreft, S. (2008). " ... Tiemann reaction: Alternatively, it is produced by condensation of phenol or its derivatives with formaldehyde to give ...
"Alcohols, phenols, and ethers". University of Nebraska-Lincoln. Britannica.com. Retrieved 22 January 2016. "12 Ways to Use ...
... and the subsequent hydrolysis of chlorobenzene to phenol. The Raschig-Hooker process is no longer used for commercial phenol ... The Raschig-Hooker process is a chemical process for the production of phenol, named after German chemist Friedrich Raschig. ... Kropf, H. (1964). "Moderne technische Phenol-Synthesen I". Chemie Ingenieur Technik - CIT. 36 (7): 759. doi:10.1002/cite. ... "Phenol". Ullmann's Encyclopedia of Industrial Chemistry. doi:10.1002/14356007.a19_299.pub2. ISBN 3527306730. Weissermel, Klaus ...
Other phenols can be used. Dichlorophenol-indophenol (DCPIP), a form of indophenol, is often used to determine the presence of ... In the Berthelot test (1859), a sample suspected of containing ammonia is treated with sodium hypochlorite and phenol. The ...
Thiophenol has a pKa of 6 vs 10 for phenol. A highly acidic thiol is pentafluorothiophenol (C6F5SH) with a pKa of 2.68. Thus, ... Collective Volume, 6, p. 979 . Melvin S. Newman and Frederick W. Hetzel (1990). "Thiophenols from Phenols: 2-Naphthalenethiol ... LiCl Phenols can be converted to the thiophenols via rearrangement of their O-aryl dialkylthiocarbamates. Many thiols are ...
"Phenols: 6-Methoxy-2-naphthol". Organic Syntheses. 49: 90. CS1 maint: Multiple names: authors list (link) ; Collective Volume, ...
"Thiophenols from Phenols: 2-Naphthalenethiol". Org. Synth. 51: 139. doi:10.15227/orgsyn.051.0139. CS1 maint: Uses authors ...
Oxidation of alcohols and phenols. As applied to electrophilic iodination, Selectfluor reagent activates the I-I bond in I2 ...
Contrary to common misconception found in organic chemistry textbooks, phenols can also be esterified to give good to near ... Other combinations of organic alcohols (such as phenol-containing compounds) and organic acids lead to a variety of different ... Hocking, M.B. (1980). "Phenyl acetate preparation from phenol and acetic acid: Reassessment of a common textbook misconception ... Offenhauer, Robert D. (1964). "The direct esterification of phenols". Journal of Chemical Education. 41: 39. Bibcode:1964JChEd ...
Organic Chemistry Nomenclature Rule C-203: Phenols "How to name organic compounds using the IUPAC rules". www.chem.uiuc.edu. ... "Alcohols, Phenols, Thiols, and Ethers". Chemistry - Louisiana Tech University. Retrieved 31 December 2013. Hans Brandenberger; ... In cases where the OH functional group is bonded to an sp2 carbon on an aromatic ring the molecule is known as a phenol, and is ... named using the IUPAC rules for naming phenols. In other less formal contexts, an alcohol is often called with the name of the ...
The naphthols are naphthalene homologues of phenol, but more reactive. Both isomers are soluble in simple alcohols, ethers, and ... Melvin S. Newman, Frederick W. Hetzel (1971). "Thiophenols from Phenols: 2-Naphthalenethiol". Org. Synth. 51: 139. doi:10.15227 ...
A phenol (1) is deprotonated with a base such as DABCO or NaH and reacted with a thiocarbamoyl chloride (2) to form an O-aryl ... Newman, M. S.; Karnes, H. A. (1966). "The Conversion of Phenols to Thiophenols via Dialkylthiocarbamates". J. Org. Chem. 31 (12 ... Melvin S. Newman, Frederick W. Hetzel (1971). "Thiophenols from Phenols: 2-Naphthalenethiol". Org. Synth. 51: 139. doi:10.15227 ...
Phenol (greater than 1.5 percent) ◦Phenol (less than 1.5 percent) ◦Poloxamer-iodine complex ◦Povidone-iodine 5 to 10 percent ◦ ... triclosan is a chlorinated aromatic compound that has functional groups representative of both ethers and phenols. Phenols ...
Aryl boronic acids or esters may be hydrolyzed to the corresponding phenols by reaction with hydroxylamine at room temperature ... A mild conversion of arylboronic acids and their pinacolyl boronate esters into phenols using hydroxylamine Ebrahim Kianmehr , ... Kidwell, R. L.; Murphy, M.; Darling, S. D. (1969). "Phenols: 6-Methoxy-2-Naphthol". Organic Syntheses. 49: 90. ; Collective ...
This oxidant is useful for the dehydrogenation of alcohols, phenols, and steroid ketones in organic chemistry. DDQ decomposes ... I. Oxidation of Monohydric Phenols". Journal of Organic Chemistry. 30 (4): 982-989. doi:10.1021/jo01015a006. Turner, A. B.; ...
Tolnaftate Goitrin Carbamate Melvin S. Newman, Frederick W. Hetzel (1971). "Thiophenols from Phenols: 2-Naphthalenethiol". Org ...
Melvin S. Newman, Frederick W. Hetzel (1971). "Thiophenols from Phenols: 2-Naphthalenethiol". Org. Synth. 51: 139. doi:10.15227 ...
R. L. Kidwell; M. Murphy; S. D. Darling (1969). "Phenols: 6-Methoxy-2-naphthol". Organic Syntheses. 49: 90. ; Collective Volume ...