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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.I'm not sure what your question is but B should be the correct answer as you've figured I guess
Its wrong
d is ans
I don't think ki D hona chahiye
iska matlab hai ki dono br nikal gaye
furthermore triangle is very unstable so its formation is ahhhh
Ya ye to tab banega jab B option ki kisi or reagent banega
exactly
himanshu pandey ka que h
Maybe the answer could be wrong
D hi hoga
There's a possibility that intramolecular wurtz goes through carbanion mechanism instead of radical so as to initiate the reaction xd
Thru carbanion mech? Ab ye konsa mech hai
do you think this bicyclo compound can be formed because of radicals joining. It is not really stable
Chemistry Stack Exchange
Why does rearrangement not take place in Wurtz reaction?
The Wurtz reaction is $$\ce{R-X + Na ->[ether] R-R}$$ where $\ce{R}$ is alkyl. But if we take butylchloride with $\ce{Na}$, the product is n-octane and not 3,4-dimethylhexane. I am unable to
for bicyclo compounds formation, it is more likely that the mechanism followed is carbanion (don't take my word for it I am just using basic logic).
we good?
+solved @!Nimay¡
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