Idea ! Though there might be a better way out; nevertheless.....
H-C≡C-H --(Na)--> HC≡CNa ---(CH3X)--> HC≡C-CH3 ----(Lindlar's)--> C=C-C ---(1mole H2O addition)--> C-C(OH)-C ---(Tautomerise)---> Acetone.....
how would you bring about the following conversion;
acetylene to acetone.
Idea ! Though there might be a better way out; nevertheless.....
H-C≡C-H --(Na)--> HC≡CNa ---(CH3X)--> HC≡C-CH3 ----(Lindlar's)--> C=C-C ---(1mole H2O addition)--> C-C(OH)-C ---(Tautomerise)---> Acetone.....
This is another way ----
acetylene + HgSO4 /H2SO4 ---------> acetone
acetone + MeMgBr ----------> 2-propanol
2-propanol + O2 + heat----------> acetone.
:) note in 3rd rxn no catalyst is required.
yes, for the no catalyst reaction, the name is "cumene hydroperoxide mechanism"