A ketone and a Grignard reagent react in ether solution followed by acid workup, to form a tertiary alcohol. Grignard reactions must be scrupulously dry in order to work effectively. A common method of drying glassware is to rinse with acetone prior to use.
1. Why is rinsing with acetone not suitable for the reaction stated in the question?a)Magnesium does not dissolve in acetone. b)Water dissolves in acetone. Adding acetone will add water to the reaction flask. c)Magnesium dissolves in acetone. Adding acetone will remove a vital reactant from the flask. d)Acetone is a ketone. Grignard reagents will react with acetone to make an unwanted byproduct.

Amines are good nucleophiles, even though they are neutral molecules. how would the rate of an sn2 reaction between an amine and an alkyl halide be affected if the polarity of the solvent is increased? amines are good nucleophiles, even though they are neutral molecules. how would the rate of an reaction between an amine and an alkyl halide be affected if the polarity of the solvent is increased? because both reactants in the rate-limiting step are neutral, the reaction will be faster if the polarity of the solvent is increased. because both reactants in the rate-limiting step are neutral, the reaction will be slower if the polarity of the solvent is increased. because both reactants in the rate-limiting step are neutral, the reaction will occur at the same rate if the polarity of the solvent is increased. request answer