b The decrease of ring strain can provide a driving force strong enough to overcompensete for the conversion of a more stable into less stable cationic centre, the carbooxonium ion $(A)$ rearranges into the carbonium ion $(B)$ because of the release of cyclo butene strain $(2 6 \,kcal/mol)$ in the formation of the cyclopentane (ring strain of about $5\, cal/mol$) cation $B$ stablizer itself by way of another $1,2$ rearrangement. The resulting action $(c)$ has comparebly little ring strain but is an electronically favourable carboxonium ion.
Download our app
and get started for free
Experience the future of education. Simply download our apps or reach out to us for more information. Let's shape the future of learning together!No signup needed.*
જ્યારે સંયોજન $HNO_3 /H_2SO_4$ સાથે નાઈટ્રેશનમાંથી પસાર થાય છે ત્યારે નાઈટ્રોનિયમ આયન -$(-NO_2)^+$ દ્વારા કઈ સ્થિતિ પર સૌથી વધુ ઝડપથી હુમલો કરવામાં આવશે