Electrophilic Aromatic Substitution

40 MCQs

MCQs

40 questions · 40 min · 40 marks

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Sample questions

The first 5 of 40. Try each one, then tap to see the answer.

  1. Question 1

    Alkanes are generally unreactive because of their:

    • APolar nature and pi bonds
    • BAromatic character
    • CIonic bonds
    • DNon-polar nature and sigma bonds only
    Show answer

    Answer: D

    Alkanes are non-polar and have only sigma bonds.

  2. Question 2

    Alkanes undergo readily in the presence of UV light:

    • AElectrophilic addition
    • BNucleophilic addition
    • CFree radical substitution
    • DElectrophilic substitution
    Show answer

    Answer: C

    UV light starts free radical substitution in alkanes.

  3. Question 3

    Alkenes are very reactive because of:

    • AThe availability of pi electrons for electrophilic reagents
    • BSigma bonds only
    • CHydrogen bonding
    • DIonic character
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    Answer: A

    The pi bond provides electrons for electrophiles.

  4. Question 4

    Alkenes typically undergo:

    • AFree radical substitution
    • BNucleophilic substitution
    • CElimination only
    • DElectrophilic addition
    Show answer

    Answer: D

    Alkenes easily undergo electrophilic addition.

  5. Question 5

    Compared with alkenes benzene is:

    • AMore reactive
    • BLess reactive because of its extra stability
    • CEqually reactive
    • DNon-aromatic
    Show answer

    Answer: B

    Benzene is very stable and thus less reactive towards electrophiles.

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