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Selective Hydrogenation of Acetophenone into Phenylethanol

Acetophenone can be selectively hydrogenated to several products, depending on the ability of the catalyst to hydrogenate the aromatic ring or the carbonyl moiety [Pg.124]

The concept of site isolation is important in catalysis. On metal particles one usually assumes that ensembles of metal atoms are necessary to activate bonds and to accommodate the fragments of molecules that tend to dissociate or to recombine. We present here three examples of such effects the dehydrogenation of decane into 1-decene, the dehydrogenation of isobutane into isobutene and the hydrogenolysis of acids or esters into aldehydes and alcohols. In most cases the effect of tin, present as a surface alloy, wiU be to dilute the active sites, reducing thereby the yield of competitive reactions. [Pg.125]


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Acetophenone, selective hydrogenation

Hydrogenation of acetophenone

Hydrogenation selectivity

Phenylethanols

Selective hydrogenation

Selectivity of hydrogenation

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