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Alkyl Halides & Aryl Halides Test - 1

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Alkyl Halides & Aryl Halides Test - 1
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Weekly Quiz Competition
  • Question 1
    1 / -0

    Which represents nucleophilic aromatic substitution reaction?

    Solution

    Two nitro groups make the nucleophilic substitution in benzene easy.

     

  • Question 2
    1 / -0

    An optically active 3-bromo-3-methyl hexane on hydrolysis gives

    Solution

    3-bromo-3-methyl hexane, on ionization gives a 3° carbocation, which can be attacked by nucleophile (H2O) to give 3-methyl-3-hexanol (optically active) as well as it can lose a proton to H2O to give 3-methyl-3-hexene.

     

     

  • Question 3
    1 / -0

    Which of the following statements about benzyl chloride is incorrect?

    Solution

    C6H5 – CH2Cl (benzyl chloride) is as reactive as allyl halide as the halogen in both cases is bonded with sp3 carbon atom and both of them are more reactive than alkyl halide.

     

  • Question 4
    1 / -0

    Tertiary alkyl halides are practically inert to substitution by SN2 mechanism because of

    Solution

    Steric hinderance due to bulky alkyl group prevents the backside attack of SN2.

     

  • Question 5
    1 / -0

    Alkyl halides react with lithium dialkyl copper reagents to give

    Solution

    R2CuLi  +  CH3CH2 – Br  →  R – CH2CH2 + RCu + LiBr

     

  • Question 6
    1 / -0

    Which of the following undergoes nucleophilic substitution exclusively by SN1mechanism?

    Solution

    Benzyl chloride forms resonance stabilized benzyl carbocation for SN1 reaction.

     

  • Question 7
    1 / -0

    The halide, which undergoes nucleophilic substitution (by SNAr mechanism) most readily is

    Solution

    The reaction proceeds by carbanion formation, which can be stabilized by electron-withdrawing groups present at ortho or para positions. The most electron- withdrawing group amongst all is – NO2.

     

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