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From Self-sufficiency
- ...or burning off. Next the smoke will go blue/grey which is the alcohols and phenols burning off. Then the smoke appears yellow, which is the tar burning off. F9 KB (1,717 words) - 19:40, 2 July 2010
- [[Category:Phenols]]8 KB (1,160 words) - 16:45, 27 September 2010
- [[Category:Phenols]]3 KB (375 words) - 15:07, 6 July 2010
- ...0 nm of the samples to the standards allows for the determination of total phenols.<ref>{{PDFlink|[http://www.users.muohio.edu/hagermae/tannin.pdf Tannin Chem20 KB (3,004 words) - 16:47, 27 September 2010
- [[Category:Phenols]]15 KB (2,005 words) - 16:49, 27 September 2010
- [[Category:Phenols]]87 KB (12,376 words) - 16:51, 27 September 2010
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- [[Category:Phenols]]1 KB (139 words) - 09:43, 20 September 2010
- [[Category:Phenols]]3 KB (379 words) - 09:43, 20 September 2010
- ...d]] to make [[coal gas]]. Coal tars are complex and variable mixtures of [[phenols]], [[polycyclic aromatic hydrocarbon]]s (PAHs), and [[heterocyclic compound5 KB (781 words) - 10:07, 20 September 2010
- [[Category:Phenols]]2 KB (195 words) - 10:10, 20 September 2010
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- [[Category:Phenols]]2 KB (296 words) - 13:10, 20 September 2010
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- [[Category:Phenols]]6 KB (713 words) - 13:15, 20 September 2010
- [[Category:Phenols]]2 KB (221 words) - 13:15, 20 September 2010
- ...ins''' are a family of [[protein]] [[toxin]]s that are soluble in [[phenol|phenols]] and produced by [[Methicillin-resistant_Staphylococcus_aureus|CA-MRSA]],1 KB (152 words) - 21:32, 20 September 2010
- | [[Phenols|Nitro or amino derivatives]] of [[phenol]] and of [[benzene]] or its [[Homo21 KB (2,852 words) - 21:33, 20 September 2010
- * [[Corrosive]] material symbol (corrosive substances e.g. acids, bases, phenols etc).1 KB (184 words) - 21:34, 20 September 2010
- ...tion with phenols gives [[phenol-formaldehyde resin]]s. With 4-substituted phenols one obtains [[calixarenes]].<ref>{{OrgSynth | last1 = Gutsche | first1 = C.34 KB (4,726 words) - 21:35, 20 September 2010
- Previously, catechol has been produced by hydrolysis of 2-substituted phenols, especially [[2-chlorophenol]], with hot aqueous solutions containing alkal ...//www.acdlabs.com/iupac/nomenclature/93/r93_414.htm R-5.5.1.1 Alcohols and phenols.]</ref>11 KB (1,437 words) - 20:14, 21 September 2010
- [[Category:Phenols]]5 KB (703 words) - 20:15, 21 September 2010
- ...nate]], Mn(acac)<sub>3</sub>, a one-electron oxidant, is used for coupling phenols.<ref name=snider/> It is prepared by the direct reaction of acetylacetone a16 KB (2,268 words) - 20:15, 21 September 2010
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- [[Category:Phenols]]5 KB (545 words) - 22:05, 21 September 2010
- ...]]s, [[alcohol]]s, and other non-polar [[organic solvent]]s. However, as [[phenols]], they form more water-soluble [[phenolate]] [[salt]]s under strongly [[al49 KB (6,487 words) - 22:06, 21 September 2010
- [[Category:Phenols]]8 KB (1,107 words) - 22:07, 21 September 2010
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- [[Category:Phenols]]21 KB (2,875 words) - 21:03, 24 September 2010
- ...eagent affects ortho-formylation of activated [[aromatic rings]] such as [[phenols]], producing aryl [[aldehyde]]s in a reaction known as the [[Reimer-Tiemann21 KB (2,827 words) - 21:03, 24 September 2010