SN1
Won't hyper conjugation make the carbocation stable? My teacher said there can't be sn1 here...
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@Dexter
Note for OP
+solved @user1 @user2... to close the thread when your doubt is solved. Mention the users who helped you solve the doubt. This will be added to their stats.Yeah i forgot to consider the 1° and OH-
Im dumb i thought H20 weak Nucleophile and the hyperconjugation stability
Alr thanks
+solved @iTeachChem
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https://www.masterorganicchemistry.com/2014/01/10/reactions-of-alkyl-halides/
You are right though. Sirf pani ke saath rxn nahi hoga.
James Ashenhurst
Master Organic Chemistry
Alkyl Halide Reaction Map And Summary
As shown in this reaction map, alkyl halides are extremely versatile. They can be converted into alcohols, thiols, ethers, azides, alkenes and more.
My oc is beginner level. Checking this it seems the reaction you have written would work only in a basic medium. OR sn1 would happen if you had a tertiary carbon.
Will wait for others’ inputs to confirm this.
@Aguilar
Alright
dekho
over here, primary carbocation will be formed so its most likely sn2, from h20, OH will attack from the back cause Cl wouldnt just get removed by itself cuz its a primary carbon, if it was a tertiary carbon then the cl would get removed without any help and it could be sn1
+solved @iTeachChem @trin
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