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Consider the compounds (I) R-I, (II) R-B...

Consider the compounds (I) R-I, (II) R-Br, (III) R-Cl, (IV) R-F. The rate of `S_(N)1` reaction is

A

`I gt II gt III gt IV `

B

`II gt I gt III gt IV `

C

`I = II = III = IV`

D

`IV gt III gt II gt I`

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The correct Answer is:
A
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MS CHOUHAN-IONIC REACTIONS (NUCLEOPHILIC SUBSTITUTION AND ELIMINATON REATIONS OF ALKYL HALIDES)-ADDITIONAL OBJECTIVE QUESTIONS (SINGLE CORRECT CHOICE TYPE)
  1. Strongest nucleophile in polar-protic solvent is

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  2. Which of the following would be true for the reaction shown ?

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  3. Consider the compounds (I) R-I, (II) R-Br, (III) R-Cl, (IV) R-F. The r...

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  4. Consider (I) CH(3) - undersetunderset(CH(3))(|)oversetoverset(CH(3)...

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  5. What is the major product of the following reaction ?

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  6. The order of reactivity of the following alkyl halides for a S(N)2 rea...

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  7. Rate of S(N)1 is maximum when X is

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  8. Reaction (I) and raection (II) are respectively,

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  9. Ph-oversetoverset(CH(3))(|)CH-undersetunderset(Br)(|)oversetoverset(CH...

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  10. Consider (i) CH(3) - undersetunderset(CH(3))(|)oversetoverset(CH(...

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  11. Maximum racemization take place when

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  12. Best leaving group is

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  13. The major product of the following reaction is

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  14. Which of the following compound will not undergo nucleophilic substitu...

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  15. Identify the final product (B) in the following reaction.

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  16. The rate of an S(N)2 reaction depends upon the

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  17. Alcoholic solution of KOH is a specific reagent for

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  18. Energy profile for the following reaction will be NH(3) + CH(3)-I t...

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  19. Best nucleophile in polar protic solvent is

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  20. Which of the following is the most reactive towards S(N)1 ?

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