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O-Methylphenol

Synonyms AI3-00137 BRN 0506917 CCRIS 646 2-Cresol o-Cresol o-Cresylic acid EINECS 202-423-8 FEMA No. 3480 l-Hydroxy-2-methylbenzene 2-Hydroxytoluene o-Hydroxytoluene 2-Methylhydroxybenzene o-Methylhydroxybenzene o-Methylphenol o-Methylphenylol NSC 23076 Orthocresol o-Oxytoluene RCRA waste number U052 2-Toluol o-Toluol UN 2076. [Pg.798]

Problem 11.17 Indicate by an arrow the position(s) most likely to undergo electrophilic substitution in each of the following compounds. List the number of the above rule(s) used in making your prediction, (a) m-xylene, (6) p-nitrotoluene, (c) m-chloronitrobenzene, (d) p-methoxytoluene, (e) p-chlorotoluene, (/) m-nilrotoluene, (g) o-methylphenol (o-cresol). [Pg.222]

Problem 11.47 Write structures for the principal mononitration products of (a) o-cresol (o-methylphenol), (b) p-CHjCONHC HjSOjH, (c) w-cyanotoluene (m-toluonitrile). ... [Pg.235]

SYNS 2-CRESOL o-CRESYLIC ACID 1-HYDROXY-2-METHYLBENZENE o-HYDROXYTOLUENE o-KRESOL (GERMAN) o-METHYLPHENOL 2-METHYLPHENOL ORTHOCRESOL o-OXYTOLUENE ORCRA WASTE NUMBER U052 o-TOLUOL... [Pg.391]

In contrast to phthalic acid, benzene nuclei without electron-withdrawing substituents, such as a carboxyl group, are hydrogenated by using hydrogen-active cathodes in acidic solutions. For example, o-methylphenol is stereoselectively hydrogenated on an Rh/ C cathode to give c/.s -2-methylcyclohexanol [42-83% yields cis—trans ratio 2.3-6.7)] as the major isomer [98],... [Pg.1060]

Sample o-Methylphenol m-Methylphenol p-Methylphenol amount Selectivity... [Pg.382]

SYNONYMS 2-cresol, o-cresylic acid, l-hydroxy-2-methylbenzene, o-hydroxytoluene, o-methylphenol, o-toluol. [Pg.60]

Methylphenol. Seep-Cresol m-Methylphenol. See m-Cresol o-Methylphenol. Seeo-Cresol p-Methylphenol. See p-Cresol... [Pg.2672]

Explain the formation of miz 90 from o-methylphenol (CH3—CeUjOH) and miz 118 from 2-methylmethylbenzoate (CH3-C6H4COOCH3). [Pg.257]

Aikyiation of Phenois. Alkylation of phenol with methanol over basic sites occurs at or /io-positions to afford o-methylphenol and 2,6-dimethylphenol, the latter being a monomer for good heat-resisting resin. The favorable catalysts are MgO and Mg-containing oxides (2,116). On the other hand, acidic catalysts give all three isomers of cresols. [Pg.412]

See other pages where O-Methylphenol is mentioned: [Pg.436]    [Pg.403]    [Pg.660]    [Pg.187]    [Pg.723]    [Pg.797]    [Pg.161]    [Pg.640]    [Pg.425]    [Pg.178]    [Pg.5099]    [Pg.100]    [Pg.695]    [Pg.1022]    [Pg.244]    [Pg.244]    [Pg.1641]   
See also in sourсe #XX -- [ Pg.349 , Pg.350 ]



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