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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 329 (1987), S. 824-832 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Thermal Reaction of Mono-n-alkyl-benzenesThe pyrolysis of ethyl-(1), n-propyl-(2), n-hexyl-(3) and n-octylbenzene (4) has been studied under conditions of steam cracking (600 to 800°C) in a laboratory scale tubular reactor. The overall activation energies determined for (1) to (4) were found to be nearly identical (221 to 227 kJ · mol-1) obviously caused by similar initial steps. The main liquid product observed was styren accompanied by ω-phenyl-1-alkenes and α-olefins. Benzene is an important side product of 1. It might be formed mainly by a hydrogen assisted dealkylation via a cyclohexadienyl type radical as reactive intermediate.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 331 (1989), S. 61-68 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Special Features in Pyrolysis Behaviour of IsoalkylaromaticsThe pyrolysis of cumene, sec. butyl- and tert. butylbenzene proceeds in a laboratory scale quartz vessel in the temperature range 600-750°C. Conversion occurs mainly via a radical-chain mechanism in the side chain in proportions, determined by the dissociation energies of the C—C- and C—H-bonds. Dealkylation was observed in greater amounts than for n-alkylbenzenes. It is interpreted by H-atom addition to the aromatic nucleus, followed by β-scission to benzene and isoalkenes. It was be shown, that H-atoms are formed by unusual reactions such as neophyl rearrangement and homolytic rupture of C—C-bonds in the side chain.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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