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Halogen Containing Compounds Test - 4

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Halogen Containing Compounds Test - 4
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Weekly Quiz Competition
  • Question 1
    4 / -1

    Which is the least reactive halide in both E1 and SN1 reaction?

    Solution

    Carbocation at bridge head carbon of bicycle compound is highly unstable due to lack of planarity.

     

  • Question 2
    4 / -1

    Reaction intermediate of E1cB reaction is:

    Solution

    E1cB take place by carbanian.

     

  • Question 3
    4 / -1

    Benzyne intermediate is not observed in

    Solution

    When aryIhalides having no hydrogen ortho to the halogen do not form benzyne intermediate.

     

  • Question 4
    4 / -1

    Solution

     

  • Question 5
    4 / -1

    The final product of the following reaction is:

    Solution

    [-M effect of NO2 group at ortho and para position]

     

  • Question 6
    4 / -1

    Identify product in the following reaction?

    Solution

     

  • Question 7
    4 / -1

    The reaction  gives the following major product

    Solution

    −CHBeing an activating group decides the position of incoming electrophile, so, E+ adds at position ortho to it as para is blocked.

     

  • Question 8
    4 / -1

    Solution

    [-M effect of -NO2 group is at para position]

     

  • Question 9
    4 / -1

    The major product of the following reaction is

    Solution

    The product (1) will be formed. Nucleophilic substitution of an alkyl halide is easier as compared to that of an aryl halide. 

    PhS− is a strong nucleophile and dimethyl formamide   is a highly polar aprotic solvent. These reagent favour SN2 reaction, the major product formed is inversion product. 

     

  • Question 10
    4 / -1

    What is the major product obtained in the following reaction?

    Solution

     

    Because aromatic halides do not give SN reaction in normal condition.

     

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