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Arrange the following three chlorides in decreasing order of SN1 reactivity
(I) CH3CH2CH2Cl

  • a)
    I > II > III
  • b)
    II > III > I
  • c)
    II > I > III
  • d)
    III > II > I
Correct answer is option 'B'. Can you explain this answer?
Most Upvoted Answer
Arrange the following three chlorides in decreasing order of SN1 react...
SN1 rxn proceeds through the formation of carbocation... greater it's stability, more is the reactivity..
For the stability of carbocation, the order is---
benzylic> allylic> tertiary> secondary> primary
This order is satisfied by option B
Thus it is the correct alternative
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