Which of the following reactions is most likely to proceed via a mechanism?
Reaction of tert-butyl bromide with aqueous sodium hydroxide
Reaction of 2-bromopropane with sodium methoxide in methanol
Reaction of methyl iodide with sodium cyanide in DMF
Reaction of 2-chloro-2-methylpropane with ethanol
Related Questions
Which of the following reactions is most likely to proceed via a mechanism?
Reaction of tert-butyl bromide with aqueous sodium hydroxide
Reaction of 2-bromopropane with sodium methoxide in methanol
Reaction of methyl iodide with sodium cyanide in DMF
Reaction of 2-chloro-2-methylpropane with ethanol
For a reaction proceeding through the SN2 mechanism, using a polar protic solvent like water will:
Increase the reaction rate
Decrease the reaction rate
Have no effect on the reaction rate
Increase the reaction temperature
The reaction is an example of an SN2 reaction. Which solvent would be least effective in promoting this reaction?
Water
DMSO
Acetone
DMF
Consider the reaction : . This reaction will be the fastest in :
water
ethanol
methanol
{\rm{N,}}\,{\rm{N'}} - dimethylformamide (DMF)
Which solvent would increase the rate of the SN2 reaction: ?
Water
Methanol
Ethanol
Acetone
The reaction will be fastest in which solvent?
Water
Ethanol
Methanol
DMF
In the SN2 reaction , which solvent will favor the reaction?
Water
Methanol
Acetonitrile
Ethanol