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Hydrogenation, catalytic bond migration with alkenes

In contrast with these results, catalytic cracking yields a much higher percentage of branched hydrocarbons. For example, the catalytic cracking of cetane yields 50-60 mol of isobutane and isobutylene per 100 mol of paraffin cracked. Alkenes crack more easily in catalytic cracking than do saturated hydrocarbons. Saturated hydrocarbons tend to crack near the center of the chain. Rapid carbon-carbon double-bond migration, hydrogen transfer to trisubstituted olefinic bonds, and extensive isomerization are characteristic.52 These features are in accord with a carbo-cationic mechanism initiated by hydride abstraction.43,55-62 Hydride is abstracted by the acidic centers of the silica-alumina catalysts or by already formed carbocations ... [Pg.34]


See other pages where Hydrogenation, catalytic bond migration with alkenes is mentioned: [Pg.1005]    [Pg.369]    [Pg.206]    [Pg.252]    [Pg.452]    [Pg.1625]    [Pg.452]    [Pg.1058]    [Pg.43]    [Pg.1624]    [Pg.392]    [Pg.452]    [Pg.913]    [Pg.252]    [Pg.953]    [Pg.222]    [Pg.306]    [Pg.76]    [Pg.98]    [Pg.320]    [Pg.277]    [Pg.1221]    [Pg.730]    [Pg.948]    [Pg.421]    [Pg.38]   
See also in sourсe #XX -- [ Pg.377 ]




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Alkene bond

Alkenes bonding

Alkenes catalytic

Alkenes catalytic hydrogenation

Alkenes hydrogenation

Bonds with hydrogen

Hydrogen migration

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