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N-Heptyl sulfide

Under the same conditions, experiments carried out with model compounds showed that benzyl sulfide underwent 100% conversion, the major product being diphenylmethane (from benzyl carbonium ion attack on benzene), whereas only 23% and 26% conversion to mixtures of unidentified compounds took place for n-heptyl sulfide and bibenzyl, respectively. [Pg.189]

NONANOL n-NONYL MERCAPTAN BUTYL-PENTYL-SULFIDE ETHYL-HEPTYL-SULFIDE HEXYL-PROPYL-SULFIDE METHYL-OCTYL-SULFIDE n-NONYLAMINE... [Pg.45]

HEPTANOL 5-HETHYL-l-HEXANOL ISOPROPYL-TERT-BUTYL-ETHER n-HEPTYL MERCAPTAN BUTYL-PROPYL-SULFIDE ETHYL-PENTYL-SULFIDE HEXYL-METHYL-SULFIDE... [Pg.69]

See other pages where N-Heptyl sulfide is mentioned: [Pg.422]    [Pg.422]    [Pg.352]    [Pg.881]    [Pg.881]    [Pg.422]    [Pg.881]    [Pg.352]    [Pg.535]    [Pg.192]   
See also in sourсe #XX -- [ Pg.62 , Pg.422 ]



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