Why Do Vinyl and Aryl Halides Not React in SN1 or SN2?

TL;DR

Vinyl and aryl halides are unreactive in SN1 and SN2 reactions due to steric hindrance and the repulsion caused by the pi electron cloud. In SN2 mechanisms, nucleophiles struggle to approach the carbon because of these factors. Additionally, the resultant carbocation from an SN1 reaction is unstable on an SP carbon, making these reactions unfavorable.

Transcript

consider the reaction between one bromel propane and potassium hydroxide in water what's going to be the major product of that reaction and will it occur via the sn2 mechanism or the sn1 mechanism what would you say so this particular type of halide it's not a typical alkyl halide this is known as a vino halide the halogen is directly attached to a... Read More

Key Insights

• 🤨 Vinyl and aryl halides are unreactive toward SN1 and SN2 reactions due to steric factors and the repulsion from the pi electron cloud.
• 🈂️ The presence of a positive charge on an SP carbon in vinyl and aryl halides creates an unstable situation.
• 🤨 Nucleophiles have difficulty approaching the carbon in vinyl halides from the back due to hinderance from the double bond system and repulsion from the pi electron cloud.

Summary & Key Takeaways

• Vinyl and aryl halides, which have a halogen directly attached to a carbon part of a double bond system, do not undergo SN1 or SN2 reactions.

• SN2 reactions are hindered due to steric factors and the repulsion from the pi electron cloud.

• SN1 reactions are not favorable as the resulting carbocation on the SP carbon is highly unstable.