Consider the substitution reaction shown below. By what mechanism will the reaction proceed? N 1 B) S N 2 C) free radical reaction D) There is not enough information to tell. class=answers-bank-image d-block rel=preload A) S N 1B) S N 2C) free radical reactionD) There is not enough information to tell.

Question

Consider the substitution reaction shown below. By what mechanism will the reaction proceed?  N 1 B)  S N 2 C)  free radical reaction D)  There is not enough information to tell. class=answers-bank-image d-block rel=preload >A)  S N 1B)  S N 2C)  free radical reactionD)  There is not enough information to tell.

Briana Smith · Accepted Answer

Final Answer : B, Explanation :  The reaction involves a nucleophilic substitution at a sp3 hybridized carbon. Specifically, an alkyl halide (R-X) is reacting with a nucleophile (OH-) to form an alcohol (R-OH). This type of reaction most commonly proceeds through an SN1 or SN2 mechanism. Based on the nature of the substrate and the nucleophile used in this reaction, it is most likely to proceed through an SN2 mechanism (S N 2).

Consider the substitution reaction shown below. By what mechanism will the reaction proceed?

A) S_N1
B) S_N2
C) free radical reaction
D) There is not enough information to tell.

Definitions

Learning Objectives

Learning Objectives

Related questions

Consider the substitution reaction shown below. By what mechanism will the reaction proceed? A) SN1B) SN2C) free radical reactionD) There is not enough information to tell.

Definitions

Learning Objectives

Learning Objectives

Related questions

Consider the substitution reaction shown below. By what mechanism will the reaction proceed?

A) S_N1
B) S_N2
C) free radical reaction
D) There is not enough information to tell.