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Allyl chloride is hydrolysed more readil...

Allyl chloride is hydrolysed more readily than n-propyl chloride. Why ?

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As we know that S1 mechanism depends uo the stability of carbocation Allyl chloride on hydrolysis gives resonance stabilised carbocaion while no resonance is observed in the carbocation formed by n-propyl chloride

Hence, allyl chloride undergoes hydrolysis much faster than n-propyl chloride.
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NCERT EXEMPLAR-HALOALKANES AND HALOARENES-Haloalkanes And Haloarenes
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  2. Which of the following compounds would undergo SN(1) reaction faster a...

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  3. Allyl chloride is hydrolysed more readily than n-propyl chloride. Why ...

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  4. Why is it necessary to avoid even traces of moisture during the use of...

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  5. How do polar solvents help in the first step in S(N)1 mechanism?

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  6. Write a test to detect the presence of double bond in a molecule.

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  12. tert-Butylbromide reacts with aq. NaOH by S(N)1 mechanism while n-buty...

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  13. Predict the major product formed when HCl is added to isobutylene, Exp...

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  14. Discuss the nature of C-X bond in the haloarenes.

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  15. How can you obtain iodoethane from ethanol when no other iodine contai...

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  16. Cyanide ion acts as an ambident nucleophille. From which end it acts a...

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  18. Match the items of Column I and Column II

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  19. Match the structures of compounds given in Column I with the classes o...

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  20. Match the reactions given in Column I with the types of reactions give...

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