The kinetics of dialkyne and chloroalkyne formation from acetylene and
methylacetylene in aqueous solutions of copper(I) and (II) chlorides
is investigated. It is found that both reactions have the same orders
with respect to [H3O+] and partial substrate pressure but have differe
nt orders with respect to [Cu(I)]SIGMA, [Cu(II)]SIGMA, and Cl(SIGMA)-.
It is shown that the nature of the background electrolyte cation has
a profound effect on the rates of both reactions. A mechanism of oxida
tive conversions of acetylene hydrocarbons is proposed.