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- W2349209323 abstract "is hydrogenated at a higher rate. In the presence of the same catalysts (with with a-allylnaphthale ne: the exception of Rh-black), isoprene and 2,3-dimethytbuta diene-l,3 are hydro1) a-propenylnaphth alene; genated at the same rate or at an even higher rate than the corresponding 2) a-allylnaphthale ne; monoolefins ((r = 0) - 3-methylbutene-1 and 2,3-dimethylbute ne-1 .[4]. On a 3) a-propylnaphthal ene, skeletal cobalt catalyst [5], the conjugated double bond of piperylene, isoprene, and 2,3-dimethylbuta diene-l,3 is hydrogenated at a higher rate than the isolated C = C bond in the corresponding monoolefin (pentene-1, 3-methylbutene-1 , and 2,3-dimethylbute ne-1). The ethylene group of vinyl cyctohexane is hydrogenated more slowly than the vinyl group of styrene, a- or fl-vinyl pyridine, in which it is conjugated with the aromatic ring [6]. Conjugation with the phenyi group increases the rate of hydrogenolysis of the trimethylene ring of phenylcyclopropane [7, 8]." @default.
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- W2349209323 date "1968-01-01" @default.
- W2349209323 modified "2023-09-27" @default.
- W2349209323 title "HYDROCARBONS IN THE PROCESS HYDROGENATION ON A RANEY NICKEL CATALYST" @default.
- W2349209323 hasPublicationYear "1968" @default.
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