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Carbocations are stabilized by nearby electron-donating groups. The stability of carbocations increases as we go from primary to secondary to tertiary carbons. Because of hyperconjugation, which invokes stabilization through donation of the electrons in C-H sigma bonds to the empty p orbital of the carbocation. Benzyl carbocation is most stable because of delocalization of charge due to resonance of π electrons in the ring. The order is Benzyl>3
o
>2
o
>1
o
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The primary benzyl radical has a very good resonance stabilisation so none of the options would compare to it , also check the attachment for order
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