Under what conditions would the reaction be most likely to proceed to the product shown at a reasonable rate? (Select one.) 
A) in a hydrocarbon solvent such as hexane
B) in ethanol solvent
C) in an ethanol solvent containing some water
D) in very dry dimethyl sulfoxide (DMSO, a polar aprotic solvent) containing a K+-bonding crown ether
E) in dimethyl sulfoxide containing a trace of water and a K+-bonding crown etherf.
in water containing enough acetone to dissolve the alkyl halide, plus a K+-bonding crown ether
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