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Q.(a) Account for the following:

(i) Tendency to show −3-3 oxidation state decreases from N to Bi in group 15.
(ii) Acidic character increases from H2OH_2O to H2TeH_2Te.
(iii) F2F_2 is more reactive than ClF3ClF_3, whereas ClF3ClF_3 is more reactive than Cl2Cl_2.
(b) Draw the structure of
(i) XeF2XeF_2,
(ii) H4P2O7H_4P_2O_7.
(OR)
(a) Give one example to show the anomalous reaction of fluorine.
(b) What is the structural difference between white phosphorus and red phosphorus?
(c) What happens when XeF6XeF_6 reacts with NaF?
(d) Why is H2SH_2S a better reducing agent than H2OH_2O?
(e) Arrange the following acids in the increasing order of their acidic character: HF, HCl, HBr and HI
CBSECBSE Class XII Board 2019Subjective· 5mImportance★★★★★
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Figure — Lewis/structural electron-dot formula of pyrophosphoric acid H4P2O7. TWO phosphorus atoms each at th
Figure — Lewis/structural electron-dot formula of pyrophosphoric acid H4P2O7. TWO phosphorus atoms each at th

Part (a): (i) inert-pair effect + falling electronegativity make −3 rarer down group 15; (ii) weaker H–E bonds and more stable conjugate bases raise acidity H2O→H2TeH_2O\to H_2Te; (iii) reactivity F2>ClF3>Cl2F_2>ClF_3>Cl_2 from weak F–F bond and polar labile Cl–F bonds; (b) XeF₂ linear, H₄P₂O₇ two bridged PO₄ tetrahedra. Part (b): F₂ oxidises water in the dark; white P = P₄, red P = polymeric; XeF6+NaF→Na[XeF7]XeF_6+NaF\to Na[XeF_7]; H₂S is a better reductant than H₂O; acidity HF<HCl<HBr<HIHF<HCl<HBr<HI.

Part (a)

(i) Tendency to show −3 decreases from N to Bi. The −3 state needs the atom to gain three electrons. Down group 15 atomic size rises and electronegativity falls sharply (N 3.0 → Bi 2.0), so the pull on extra electrons weakens. The inert-pair effect (the ns2ns^2 pair is reluctant to engage in bonding for heavy elements) makes As, Sb, Bi favour +3/+5 instead; Bi shows essentially no −3 chemistry.

(ii) Acidic character increases HX2O→HX2Te\ce{H2O -> H2Te}. Acidity depends on how easily the H–E bond ionises. Bond strengths fall H–O (464) > H–S (347) > H–Se (276) > H–Te (238 kJ mol⁻¹) because orbital overlap worsens with the larger central atom. Weaker bonds release HX+\ce{H+} more readily, and the bigger conjugate base (TeX2−>OX2−\ce{Te^2-} > \ce{O^2-}) disperses charge better. So HX2O\ce{H2O} is neutral while acidity rises to HX2Te\ce{H2Te}.

(iii) FX2>ClFX3>ClX2\ce{F2 > ClF3 > Cl2}. FX2\ce{F2} has the weakest halogen bond (lone-pair repulsion in the tiny molecule) and highest electronegativity → extremely reactive. The interhalogen ClFX3\ce{ClF3} has polar, weak, labile Cl–F bonds and a T-shape that readily delivers fluorine, so it exceeds ClX2\ce{Cl2}, whose strong, non-polar Cl–Cl bond makes it least reactive of the three.

(b) Structures.

  • (i) XeFX2\ce{XeF2} — 5 electron pairs on Xe (2 bonds + 3 lone pairs) in a trigonal-bipyramidal set; the 3 lone pairs take equatorial sites, giving a linear molecule, F–Xe–F = 180°. …

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