Would you expect acetate ion CH3CO2 to be a better nucleophile in an SN2 reaction with an alkyl halide carried out in methanol or in dimethyl sulfoxide?

What is the first step in an SN1 reaction? Group of answer choices Attack of the nucleophile. Loss of the leaving group. Protonation of the leaving group.

Polar aprotic solvents enhance the rate of an SN2 reaction by stabilizing the cations and the anions. changing the polarizibility of the nucleophile. raising the energy of the nucleophile. O lowering the energy of the nucleophile. Save for Later

Which mechanism, E1 or E2, will occur in attached reaction?

Which of these nucleophiles would be the best for converting a tertiary alkyl halide into an alcohol? CH3O- CH3OH H3O+ OH- H2O

In an SN2 reaction, which of the following nucleophiles will produce an ether? "C=CH HO. "O-C-CH3 O "OCH2CH3 excess NH3

Which is best nucleophile?

HCOO- > HO- > (CH3)2 Sort from best nucleophile to worst nucleophile

Provide the necessary alkyl bromide and alkoxide needed to complete this SN2 reaction. + Edit the Alkyl Bromide + ºe Draw Nucleophile i THF хо Q

How could you change the reaction conditions given to most strongly favor an E2 mechanism? Br H₂O Use a higher concentration of water Use a stronger base Add a stronger nucleophile O Use a tertiary alkyl halide O Increase the concentration of the reactant