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NEET-UG and JEE Main Chemistry · Class 11

Anomalous first-member behaviour and the inert pair effect — NEET & JEE Questions

Anomalous first-member behaviour and the inert pair effect is a topic in p-Block Elements, a Class 11 Chemistry chapter of the NEET-UG and JEE Main syllabus. TestBudy holds 12 published NEET-UG and JEE Main questions on Anomalous first-member behaviour and the inert pair effect, each with the marking scheme of the real paper.

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Anomalous first-member behaviour and the inert pair effect MCQs with solutions

10 of the 12 published questions on this topic, exactly as they appear in a test. Answers and worked solutions come with your result rather than on this page.

  1. Question 1 · difficulty L1 · recall

    The inert pair effect refers to the tendency of the outermost ns2ns^2 electron pair in heavier p-block elements to

    • A. remain less available for bonding
    • B. become more reactive than all p electrons
    • C. always be removed first
    • D. form only ionic bonds
  2. Question 2 · difficulty L2 · understanding

    First members of p-block groups often show anomalous behaviour mainly because of their

    • A. small size, high electronegativity and absence of accessible d orbitals in the valence shell
    • B. very large size only
    • C. low ionisation enthalpy only
    • D. complete metallic character
  3. Question 3 · difficulty L2 · understanding

    The inert pair effect generally becomes more important

    • A. down a p-block group
    • B. from bottom to top only
    • C. only in period 2
    • D. only in noble gases
  4. Question 4 · difficulty L2 · understanding

    Because of the inert pair effect, heavier p-block elements often show increased stability of

    • A. oxidation states two units lower than the group maximum
    • B. only the highest oxidation state
    • C. zero oxidation state only
    • D. negative oxidation states exclusively
  5. Question 5 · difficulty L3 · application

    Which oxidation state becomes especially stable for thallium because of the inert pair effect?

    • A. +1
    • B. +2
    • C. +3
    • D. +5
  6. Question 6 · difficulty L3 · application

    For lead, the inert pair effect helps explain the relatively high stability of

    • A. +2 compared with +4 in heavier chemistry
    • B. +4 only
    • C. +1 only
    • D. +6
  7. Question 7 · difficulty L3 · application

    Why does nitrogen differ markedly from heavier Group 15 elements in some bonding patterns?

    • A. Its small size and lack of valence d orbitals contribute to anomalous behaviour
    • B. It is the largest Group 15 atom
    • C. It has the strongest inert pair effect in the group
    • D. It is metallic
  8. Question 8 · difficulty L3 · application

    Which statement best describes the trend in stability of Group 13 oxidation states down the group?

    • A. The +1 state generally becomes more stable relative to +3
    • B. The +3 state becomes exclusively more stable
    • C. The +5 state becomes dominant
    • D. Oxidation states become impossible
  9. Question 9 · difficulty L4 · application

    Why is Pb4+Pb^{4+} often a stronger oxidising species than Pb2+Pb^{2+}?

    • A. Pb(II) is stabilised by the inert pair effect, so Pb(IV) tends to be reduced to Pb(II)
    • B. Pb(IV) contains no electrons
    • C. Pb(II) is always unstable
    • D. Pb(IV) cannot accept electrons
  10. Question 10 · difficulty L4 · application

    Which comparison best illustrates anomalous first-member behaviour?

    • A. A second-period p-block element differs strongly from heavier congeners because of small size and inability to expand its valence shell
    • B. The heaviest member exactly duplicates the first
    • C. All group members have identical chemistry
    • D. An anomaly must be caused only by nuclear mass

Common mistakes in Anomalous first-member behaviour and the inert pair effect

Recorded against questions in this topic that are not shown above, so none of these points at an answer you can see on this page.

  • Reverses the inert-pair trend and predicts increasing preference for the maximum oxidation state.
  • Explains the lower oxidation states using unrelated size trends instead of the common ns2-pair effect.

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