The stability of carbanions in the following
i) RC≡⊖C
ii)
iii) R2C=⊖CH
iv) R3C−⊖CH2
is in the order of
(i) > (ii) > (iii) > (iv)
(ii) > (iii) > (iv) > (i)
(iv) > (ii) > (iii) > (i)
(i) > (iii) > (ii) > (iv)
The carbanion with more s-character is more stable. Thus, the order of stability is
RC≡⊖C>C6H⊖5>R2C=⊖CH>R3C−⊖CH2
Innucleophilic addition reactions, the reactivities of carbonyl compounds NO2CH2CHO(I), ClCH2CHO(II), CH3CHO(III) and CH3CH2CHO (IV) are in the order of
The correct order for decreasing stability of the following free radicals is