Why do benzylic halides show high reactivity towards SN1 mechanism?
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Ben jealous healthy so high reactive towards SN1 machines of compound pressure of the heat and light sometimes of the multiple reflection of light and sound of the heat pressure so that it is a solution is very high pressure.
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Welcome dear,
● Explaination -
- In SN1 reaction, carbocation intermediates are formed.
- In benzyl carbocation, positive charge is delocalized on the benzene ring with resonance. This makes them more stable.
- Here, it becomes easy for nucleophile to attack the carbocation and form products.
- Therefore, benzyl halides readily undergo SN1 reaction.
Hope this helps you.
Keep asking.
● Explaination -
- In SN1 reaction, carbocation intermediates are formed.
- In benzyl carbocation, positive charge is delocalized on the benzene ring with resonance. This makes them more stable.
- Here, it becomes easy for nucleophile to attack the carbocation and form products.
- Therefore, benzyl halides readily undergo SN1 reaction.
Hope this helps you.
Keep asking.
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