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Carbocation as an intermediate is likely...

Carbocation as an intermediate is likely to be formed in the reaction :

A

`"Hexene"overset("Anhyd. AlCl"_(3)//HCl)rarr"2-chloro-2-methylpentane"`

B

`"Propene"+Cl_(2)overset(hv)rarr"2-chloropropane"`

C

`"Ethyl bromide"+KOH(aq.)overset(Delta)rarr"ethyl alcohol"`

D

`"Acetone + HCN"overset(.^(-)OH)rarr"acetonecyanohydrin"`

Text Solution

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The correct Answer is:
A
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OP TANDON-BASIC PRINCIPLES OF ORGANIC COMPOUNDS (MECHANISM OF ORGANIC REACTIONS)-OBJECTIVE QUESTIONS (Level-A)
  1. Among the following carbocations : (I) Ph(2)overset(+)"C"CH(2)Me (II...

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  2. Which one of the following characteristics belongs to an electrophile?

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  3. Carbocation as an intermediate is likely to be formed in the reaction ...

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  4. Which of the following pK(a) values, represents the strongest acid?

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  5. Which of the following orders regarding relative stability of free rad...

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  6. Which of the following is the strongest base?

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  7. Which of the following is least reactive in a nucleophilic substitutio...

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  8. In the compound given below: the correct order of acidity of the posit...

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  9. Due to the presence of an unpaired electron, free radicals are:

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  10. Among the following the strongest nucleophilic is

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  11. Which one of the following is most reactive towards nucleophilic subst...

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  12. Strength of acidity is in order:

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  13. Which is most stable carbocation?

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  14. Which of the following undergoes nucleophilic substitution exclusively...

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  15. In the S(N^(1)) reaction on chiral centres there is :

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  16. Which one of the following halogen compounds is difficult to be hydrol...

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  17. The stability of Me(2)C=CH(2) is more than that of MeCH(2)CH=CH(2) due...

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  18. CH(3)Br+Nu^(-)rarrCH(3)Nu+Br^(-) The decreasing order of the rate of...

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  19. The increasing order of stability of the following free radicals is :

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  20. Which of the following is more basic than aniline?

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