Sodium Iodide In Acetone Sn2. Web the addition of sodium or potassium iodide catalyzes many sn2 reactions of alkyl chlorides or bromides. Web the addition of sodium or potassium iodide catalyzes many sn2 reactions of alkyl chlorides or bromides.
I think the reason why it catalyzes many sn2. The best solvent for − c l to − i conversion is usually acetone. This problem has been solved!. Web the addition of sodium or potassium iodide catalyzes many sn2 reactions of alkyl chlorides or bromides. Web the addition of sodium or potassium iodide catalyzes many sn2 reactions of alkyl chlorides or bromides. Propose a mechanism for the reaction above. The primary alkyl halide will react by means. Web the conversion from m e c l to m e i go through s n 2 mechanism. It is cheap, polar aprotic, good. Also, sodium iodide, nai, is soluble in acetone.
Web each compound will be treated with a solution of sodium iodide (excellent nucleophile) in acetone (polar, aprotic solvent). Also, sodium iodide, nai, is soluble in acetone. Web the conversion from m e c l to m e i go through s n 2 mechanism. It is cheap, polar aprotic, good. Propose a mechanism for the reaction above. The primary alkyl halide will react by means. Web the addition of sodium or potassium iodide catalyzes many sn2 reactions of alkyl chlorides or bromides. Web each compound will be treated with a solution of sodium iodide (excellent nucleophile) in acetone (polar, aprotic solvent). I think the reason why it catalyzes many sn2. Web see answer sn2, sodium iodide in acetone (nai in acetone sn1, silver nitrate in ethanol (agno3 in etoh) with these: The best solvent for − c l to − i conversion is usually acetone.
