Stability of radical depends on the hyperconjugation and resonance.Higher the hyperconjugating structure higher will be the stability.we know, 3° radical is most stable than that of 2° and at last 1° radical.
Here, radical A and radical C is 3° radical.Radical B is 1° radical.So, radical B is least stable.
Between A and C, A show resonance structure but C could not.Therefore,A is most stable radical.
Stability order is A>C>B
Rank the following radicals in order of decreasing stability. A B с A: (Select] V B:...
Rank the following radicals in order of decreasing
stability.
Rank the following radicals in order of decreasing stability.
Rank the following radicals in order of decreasing
stability.
Rank the following radicals in order of decreasing stability.
Rank the following radicals in order of decreasing
stability.
Link the following radicals in order of decreasing stability.
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rank the most stable radicals in order of decreasing
stability
9 N Sapling Learning Casperset Minnesota State University, Moorhead Rank the following radicals in order of decreasing stability, most stable least stable (CH) CHCH.CH, (CH),CHCHCH (CH),"CH.CH Previous ven & View Solution Check
2. Rank the following radicals in decreasing order of stability (1-most stable, 5-least stable): CH2 CH3 (CH3)2Ć (CH3)2CH CH3CH2
Rank the following carbocations in order of decreasing
stability.
Rank the following carbocations in order of decreasing stability.
Rank the following carbocations in order of decreasing stability. Rank the following carbocations in order of decreasing stability. (CH3)2CCH2CH3 CH3CH2CH-CH CH3CH-CCH3 2 143 34>2> 1 2>1>3>4 4321
Rank the following carbocations in order of decreasing stability.
Rank the following carbocations in order of decreasing stability.