Choose the correct order of stability for the following carbocations.
A
(a)>(b)>(c)
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B
(c)>(b)>(a)
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C
(b)>(c)>(a)
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D
(a)>(c)>(b)
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Solution
The correct option is B(c)>(b)>(a) For compound (a), carbocation is at bridge head position, it is the least stable because presence of carbocation creates a strain at the already strained position.
For structure (c), there are 8 α-hydrogens, whereas in structure (b) there are 3 α-hydrogens.
So, structure (c) will have more hyperconjugative structures and more will be the stability. The correct order for the stability is: (c)>(b)>(a)