2) A given complex MLn forms only a dihydrogen complex (n2-H2)MLn, not the true oxidative addition product (H)2MLn with H2. Would the true oxidative addition product be more or less likely to form as we move to (a) more electron-releasing ligands L, (b) from a third- to a first-row metal, M, (c) to the 1 electron oxidation product [H2MLn]? Would you expect the same metal fragment above to form an ethylene complex, (C2H4)MLn, with predominantly Dewar-Chatt or metalacyclopropane character? Explain all your results.

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2) A given complex MLn forms only a dihydrogen complex (n²-H2)MLn, not the true
oxidative addition product (H)2MLn with H2. Would the true oxidative addition
product be more or less likely to form as we move to (a) more electron-releasing
ligands L, (b) from a third- to a first-row metal, M, (c) to the 1 electron oxidation
product [H2MLn]*? Would you expect the same metal fragment above to form
an ethylene complex, (C2H4)MLn, with predominantly Dewar-Chatt or
metalacyclopropane character? Explain all your results.
Transcribed Image Text:2) A given complex MLn forms only a dihydrogen complex (n²-H2)MLn, not the true oxidative addition product (H)2MLn with H2. Would the true oxidative addition product be more or less likely to form as we move to (a) more electron-releasing ligands L, (b) from a third- to a first-row metal, M, (c) to the 1 electron oxidation product [H2MLn]*? Would you expect the same metal fragment above to form an ethylene complex, (C2H4)MLn, with predominantly Dewar-Chatt or metalacyclopropane character? Explain all your results.
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