{"id":12756,"date":"2025-09-22T13:29:20","date_gmt":"2025-09-22T12:29:20","guid":{"rendered":"https:\/\/mcqsadda.com\/?p=12756"},"modified":"2025-10-22T10:16:24","modified_gmt":"2025-10-22T09:16:24","slug":"chemical-bonding-top-100-mcqs-with-answer-and-explanation","status":"publish","type":"post","link":"https:\/\/mcqsadda.com\/index.php\/2025\/09\/22\/chemical-bonding-top-100-mcqs-with-answer-and-explanation\/","title":{"rendered":"Chemical bonding Top 100 MCQs With Answer and Explanation"},"content":{"rendered":"\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">1. Which type of bond is formed by transfer of electrons?<\/mark><\/strong><br>A) Ionic bond<br>B) Covalent bond<br>C) Metallic bond<br>D) Hydrogen bond<br><strong>Answer: A<\/strong><br><strong>Explanation<\/strong><em>:<\/em> Ionic bonds form due to complete transfer of electrons from one atom to another.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">2. Ionic bond is generally formed between:<\/mark><\/strong><br>A) Metal &amp; Non-metal<br>B) Metal &amp; Metal<br>C) Non-metal &amp; Non-metal<br>D) Noble gases<br><strong>Answer: A<\/strong><br><strong>Explanation<\/strong>: Metals lose electrons, non-metals gain electrons \u2192 ionic bond.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">3. Which of the following is an example of ionic compound?<\/mark><\/strong><br>A) HCl<br>B) NaCl<br>C) H\u2082O<br>D) CO\u2082<br><strong>Answer: B<\/strong><br><strong>Explanation<\/strong>: NaCl is ionic due to transfer of electron from Na to Cl.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">4. A covalent bond is formed due to:<\/mark><\/strong><br>A) Transfer of electrons<br>B) Sharing of electrons<br>C) Overlapping of orbitals<br>D) Both B &amp; C<br><strong>Answer: D<\/strong><br><strong>Explanation<\/strong>: Covalent bond is formed by sharing electrons via orbital overlap.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">5. Which of the following is a covalent compound?<\/mark><\/strong><br>A) NaCl<br>B) MgO<br>C) HCl<br>D) CaF\u2082<br><strong>Answer: C<\/strong><br><strong>Explanation<\/strong>: HCl forms covalent bond by sharing electrons.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">6. The bond energy is:<\/mark><\/strong><br>A) Energy released in bond formation<br>B) Energy required to break a bond<br>C) Energy of atom<br>D) None of these<br><strong>Answer: B<\/strong><br><strong>Explanation<\/strong>: Bond energy = minimum energy needed to break one mole of bonds.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">7. Bond length is:<\/mark><\/strong><br>A) Distance between nuclei of bonded atoms<br>B) Sum of radii<br>C) Difference of radii<br>D) None<br><strong>Answer: A<\/strong><br><strong>Explanation: <\/strong>Bond length is internuclear distance at minimum energy.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">8. Bond order in N\u2082 molecule is:<\/mark><\/strong><br>A) 1<br>B) 2<br>C) 3<br>D) 4<br><strong>Answer: C<\/strong><br>Explanation: N\u2082 has triple bond \u2192 bond order = 3.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">9. Higher bond order means:<\/mark><\/strong><br>A) Shorter bond length<br>B) Higher bond energy<br>C) Stronger bond<br>D) All of these<br><strong>Answer: D<\/strong><br><strong>Explanation<\/strong>: Bond order \u2191 \u2192 bond length \u2193, bond energy \u2191, strength \u2191.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">10. Which has highest bond order?<\/mark><\/strong><br>A) O\u2082<br>B) O\u2082\u207a<br>C) O\u2082\u207b<br>D) O\u2082\u00b2\u207b<br><strong>Answer: B<\/strong><br><strong>Explanation<\/strong>: O\u2082\u207a has bond order 2.5 (highest among these).<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">11. Which is most stable?<\/mark><\/strong><br>A) N\u2082<br>B) O\u2082<br>C) F\u2082<br>D) Cl\u2082<br><strong>Answer: A<\/strong><br><strong>Explanation<\/strong>: N\u2082 has highest bond order (3) \u2192 most stable.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">12. Ionic compounds are generally:<\/mark><\/strong><br>A) Soluble in non-polar solvents<br>B) Soluble in polar solvents<br>C) Insoluble in water<br>D) Covalent in nature<br><strong>Answer: B<\/strong><br><strong>Explanation<\/strong>: Ionic compounds dissolve in polar solvents like water.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">13. Covalent compounds generally have:<\/mark><\/strong><br>A) High melting point<br>B) Low melting point<br>C) Metallic properties<br>D) Conductivity in solid state<br><strong>Answer: B<\/strong><br><strong>Explanation<\/strong>: Covalent compounds have weak intermolecular forces \u2192 low melting points.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">14. Which has the smallest bond length?<\/mark><\/strong><br>A) N\u2261N<br>B) O=O<br>C) F\u2013F<br>D) Cl\u2013Cl<br><strong>Answer: A<\/strong><br>Explanation: Triple bond \u2192 shortest bond length.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">15. Metallic bond theory is explained by:<\/mark><\/strong><br>A) Electron sea model<br>B) Valence bond theory<br>C) Hybridization<br>D) MOT<br><strong>Answer: A<\/strong><br><strong>Explanation<\/strong>: Metallic bonding is explained by free electrons in a sea model.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">16. Which has both ionic &amp; covalent bonds?<\/mark><\/strong><br>A) NaCl<br>B) K\u2082SO\u2084<br>C) NH\u2084Cl<br>D) H\u2082O<br><strong>Answer: C<\/strong><br><strong>Explanation<\/strong>: NH\u2084Cl has covalent N\u2013H bonds and ionic NH\u2084\u207aCl\u207b bonding.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">17. Bond angle in H\u2082O is approximately:<\/mark><\/strong><br>A) 180\u00b0<br>B) 120\u00b0<br>C) 109.5\u00b0<br>D) 104.5\u00b0<br><strong>Answer: D<\/strong><br><strong>Explanation<\/strong>: Due to 2 lone pairs, bond angle reduces to 104.5\u00b0.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">18. Bond angle in NH\u2083 is:<\/mark><\/strong><br>A) 120\u00b0<br>B) 109.5\u00b0<br>C) 107\u00b0<br>D) 90\u00b0<br><strong>Answer: C<\/strong><br><strong>Explanation<\/strong>: NH\u2083 (sp\u00b3 hybridised, 1 lone pair) \u2192 bond angle 107\u00b0.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">19. Which has linear geometry?<br><\/mark><\/strong>A) CO\u2082<br>B) NH\u2083<br>C) H\u2082O<br>D) BF\u2083<br><strong>Answer: A<\/strong><br><strong>Explanation<\/strong>: CO\u2082 is sp hybridised, linear (180\u00b0).<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">20. Bond angle in BF\u2083 is:<br><\/mark><\/strong>A) 120\u00b0<br>B) 109.5\u00b0<br>C) 104.5\u00b0<br>D) 90\u00b0<br><strong>Answer: A<\/strong><br><strong>Explanation<\/strong>: BF\u2083 is sp\u00b2 hybridised \u2192 trigonal planar, 120\u00b0.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">21. Which bond is strongest?<\/mark><\/strong><br>A) Ionic bond<br>B) Covalent bond<br>C) Metallic bond<br>D) Hydrogen bond<br><strong>Answer: A<\/strong><br><strong>Explanation:<\/strong> Ionic bonds are generally strongest due to electrostatic attraction.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">22. Which molecule has polar covalent bond?<\/mark><\/strong><br>A) H\u2082<br>B) Cl\u2082<br>C) HCl<br>D) O\u2082<br><strong>Answer: C<\/strong><br><strong>Explanation: <\/strong>H\u2013Cl bond is polar due to electronegativity difference.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">23. Which molecule has non-polar covalent bond?<\/mark><\/strong><br>A) HCl<br>B) H\u2082O<br>C) F\u2082<br>D) NH\u2083<br><strong>Answer: C<\/strong><br><strong>Explanation<\/strong><em><strong>:<\/strong><\/em> F\u2082 has equal sharing (same atoms) \u2192 non-polar.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">24. Lattice energy of ionic compounds depends on:<\/mark><\/strong><br>A) Size of ions<br>B) Charge of ions<br>C) Distance between ions<br>D) All of these<br><strong>Answer: D<\/strong><br><strong>Explanation: <\/strong>Lattice energy \u221d q\u2081q\u2082 \/ r.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">25. Which has highest lattice energy?<\/mark><\/strong><br>A) NaCl<br>B) MgO<br>C) KCl<br>D) CaO<br><strong>Answer: B<\/strong><br><strong>Explanation: <\/strong>Mg\u00b2\u207aO\u00b2\u207b has highest charges \u2192 highest lattice energy.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">26. The VSEPR theory is used to predict:<\/mark><\/strong><br>A) Bond energy<br>B) Bond order<br>C) Shape of molecules<br>D) Lattice energy<br><strong>Answer: C<\/strong><br><strong>Explanation:<\/strong> VSEPR theory predicts molecular geometry based on repulsion between electron pairs.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">27. According to VSEPR theory, shape of BeCl\u2082 is:<\/mark><\/strong><br>A) Linear<br>B) Bent<br>C) Trigonal planar<br>D) Tetrahedral<br><strong>Answer: A<\/strong><br><strong>Explanation:<\/strong> BeCl\u2082 has 2 bond pairs, no lone pairs \u2192 linear (180\u00b0).<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">28. Shape of BF\u2083 is:<\/mark><\/strong><br>A) Linear<br>B) Trigonal planar<br>C) Tetrahedral<br>D) Pyramidal<br><strong>Answer: B<br>Explanation: <\/strong>BF\u2083 is sp\u00b2 hybridised, 120\u00b0 bond angle \u2192 trigonal planar.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">29. The shape of CH\u2084 molecule is:<\/mark><\/strong><br>A) Trigonal planar<br>B) Square planar<br>C) Tetrahedral<br>D) Linear<br><strong>Answer: C<\/strong><br><strong>Explanation: <\/strong>CH\u2084 is sp\u00b3 hybridised, tetrahedral (109.5\u00b0).<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">30. Hybridisation of carbon in CH\u2084 is:<\/mark><\/strong><br>A) sp<br>B) sp\u00b2<br>C) sp\u00b3<br>D) dsp\u00b2<br><strong>Answer: C<\/strong><br><strong>Explanation: <\/strong>CH\u2084 has 4 sigma bonds \u2192 sp\u00b3 hybridisation.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">31. The shape of NH\u2083 molecule is:<\/mark><\/strong><br>A) Linear<br>B) Trigonal planar<br>C) Pyramidal<br>D) Tetrahedral<br><strong>Answer: C<\/strong><br><strong>Explanation:<\/strong> NH\u2083 has sp\u00b3 hybridisation, one lone pair \u2192 pyramidal (107\u00b0).<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">32. The shape of H\u2082O molecule is:<\/mark><\/strong><br>A) Linear<br>B) Bent<br>C) Tetrahedral<br>D) Trigonal planar<br><strong>Answer: B<\/strong><br><strong>Explanation: <\/strong>H\u2082O has sp\u00b3 hybridisation, two lone pairs \u2192 bent (104.5\u00b0).<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">33. Which has trigonal bipyramidal geometry?<\/mark><\/strong><br>A) PCl\u2085<br>B) SF\u2086<br>C) ClF\u2083<br>D) XeF\u2082<br><strong>Answer: A<\/strong><br><strong>Explanation: <\/strong>PCl\u2085 is sp\u00b3d hybridised \u2192 trigonal bipyramidal.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">34. Which has octahedral geometry?<\/mark><\/strong><br>A) PCl\u2085<br>B) SF\u2086<br>C) XeF\u2082<br>D) IF\u2083<br><strong>Answer: B<\/strong><br><strong>Explanation: <\/strong>SF\u2086 is sp\u00b3d\u00b2 hybridised \u2192 octahedral.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">35. Hybridisation of Xe in XeF\u2082 is:<\/mark><\/strong><br>A) sp\u00b3<br>B) sp\u00b3d<br>C) sp\u00b3d\u00b2<br>D) sp\u00b3d\u00b3<br><strong>Answer: B<\/strong><br><strong>Explanation: <\/strong>XeF\u2082 \u2192 sp\u00b3d hybridisation, linear shape.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">36. Shape of ClF\u2083 is:<\/mark><\/strong><br>A) Linear<br>B) T-shaped<br>C) Trigonal planar<br>D) Octahedral<br><strong>Answer: B<br>Explanation: <\/strong>ClF\u2083 has sp\u00b3d hybridisation with 2 lone pairs \u2192 T-shaped.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">37. Hybridisation in SF\u2084 is:<\/mark><\/strong><br>A) sp\u00b3<br>B) sp\u00b3d<br>C) sp\u00b3d\u00b2<br>D) sp\u00b3d\u00b3<br><strong>Answer: B<\/strong><br><strong>Explanation: <\/strong>SF\u2084 is sp\u00b3d hybridised, seesaw shape.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">38. Shape of SF\u2084 is:<\/mark><\/strong><br>A) Linear<br>B) Seesaw<br>C) Square planar<br>D) T-shaped<br><strong>Answer: B<\/strong><br><strong>Explanation: <\/strong>SF\u2084 (sp\u00b3d) has one lone pair \u2192 seesaw geometry.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">39. In XeF\u2084, the geometry is:<\/mark><\/strong><br>A) Square planar<br>B) Octahedral<br>C) Tetrahedral<br>D) Trigonal bipyramidal<br><strong>Answer: A<\/strong><br><strong>Explanation:<\/strong><em> <\/em>XeF\u2084 has sp\u00b3d\u00b2 hybridisation with 2 lone pairs \u2192 square planar.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">40. Which molecule has square pyramidal shape?<\/mark><\/strong><br>A) XeF\u2082<br>B) XeF\u2084<br>C) IF\u2085<br>D) SF\u2086<br><strong>Answer: C<\/strong><br><strong>Explanation:<\/strong> IF\u2085 is sp\u00b3d\u00b2 hybridised with one lone pair \u2192 square pyramidal.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">41. The shape of XeF\u2086 is:<\/mark><\/strong><br>A) Octahedral<br>B) Distorted octahedral<br>C) Square planar<br>D) Trigonal bipyramidal<br><strong>Answer: B<\/strong><br><strong>Explanation:<\/strong> XeF\u2086 is sp\u00b3d\u00b3 hybridised with one lone pair \u2192 distorted octahedral.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">42. Which of the following is non-linear?<\/mark><\/strong><br>A) CO\u2082<br>B) BeCl\u2082<br>C) H\u2082O<br>D) C\u2082H\u2082<br><strong>Answer: C<\/strong><br><strong>Explanation: <\/strong>H\u2082O has bent shape, others are linear.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\"><strong>43. Hybridisation of C in C\u2082H\u2082 is:<\/strong><\/mark><br>A) sp\u00b3<br>B) sp\u00b2<br>C) sp<br>D) dsp\u00b2<br><strong>Answer: C<\/strong><br><strong>Explanation: <\/strong>C in acetylene (C\u2082H\u2082) is sp hybridised (linear).<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">44. Hybridisation of C in C\u2082H\u2084 is:<\/mark><\/strong><br>A) sp\u00b3<br>B) sp\u00b2<br>C) sp<br>D) dsp\u00b2<br><strong>Answer: B<\/strong><br><strong>Explanation: <\/strong>Ethene has double bond \u2192 sp\u00b2 hybridisation.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">45. Hybridisation of C in C\u2082H\u2086 is:<\/mark><\/strong><br>A) sp\u00b3<br>B) sp\u00b2<br>C) sp<br>D) dsp\u00b2<br><strong>Answer: A<\/strong><br><strong>Explanation:<\/strong> Ethane has only single bonds \u2192 sp\u00b3 hybridisation.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\"><strong>46. The bond angle in sp\u00b3 hybridisation (ideal) is:<\/strong><\/mark><br>A) 90\u00b0<br>B) 109.5\u00b0<br>C) 120\u00b0<br>D) 180\u00b0<br><strong>Answer: B<\/strong><br><strong>Explanation: <\/strong>sp\u00b3 \u2192 tetrahedral \u2192 109.5\u00b0.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\"><strong>47. The bond angle in sp\u00b2 hybridisation is:<\/strong><\/mark><br>A) 90\u00b0<br>B) 109.5\u00b0<br>C) 120\u00b0<br>D) 180\u00b0<br><strong>Answer: C<\/strong><br><strong>Explanation:<\/strong> sp\u00b2 \u2192 trigonal planar \u2192 120\u00b0.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\"><strong>48. The bond angle in sp hybridisation is:<\/strong><\/mark><br>A) 90\u00b0<br>B) 109.5\u00b0<br>C) 120\u00b0<br>D) 180\u00b0<br><strong>Answer: D<\/strong><br><strong>Explanation: <\/strong>sp \u2192 linear \u2192 180\u00b0.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">49. In NH\u2084\u207a ion, the hybridisation of N is:<\/mark><\/strong><br>A) sp\u00b2<br>B) sp\u00b3<br>C) sp\u00b3d<br>D) sp\u00b3d\u00b2<br><strong>Answer: B<\/strong><br><strong>Explanation: <\/strong>NH\u2084\u207a has 4 sigma bonds, no lone pairs \u2192 sp\u00b3 hybridisation.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">50. Which of the following is trigonal pyramidal?<\/mark><\/strong><br>A) BF\u2083<br>B) NH\u2083<br>C) CH\u2084<br>D) CO\u2082<br><strong>Answer: B<\/strong><br><strong>Explanation: <\/strong>NH\u2083 has sp\u00b3 hybridisation with one lone pair \u2192 trigonal pyramidal.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">51. Valence Bond Theory (VBT) explains bond formation by:<\/mark><\/strong><br>A) Sharing of electrons<br>B) Transfer of electrons<br>C) Overlap of atomic orbitals<br>D) Lattice formation<br><strong>Answer: C<\/strong><br><strong>Explanation: <\/strong>VBT states that covalent bonds are formed by overlapping of atomic orbitals containing unpaired electrons.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">52. The overlapping of orbitals along the internuclear axis forms:<\/mark><\/strong><br>A) \u03c0-bond<br>B) \u03c3-bond<br>C) Ionic bond<br>D) Metallic bond<br><strong>Answer: B<\/strong><br><strong>Explanation: <\/strong>End-to-end overlap \u2192 sigma (\u03c3) bond.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\"><strong>53. Sidewise overlap of orbitals forms:<\/strong><\/mark><br>A) \u03c3-bond<br>B) \u03c0-bond<br>C) Ionic bond<br>D) Hydrogen bond<br><strong>Answer: B<\/strong><br>Explanation: Side-by-side overlap \u2192 pi (\u03c0) bond.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">54. Which bond is stronger?<\/mark><\/strong><br>A) \u03c3-bond<br>B) \u03c0-bond<br>C) Both equal<br>D) None<br><strong>Answer: A<\/strong><br>Explanation: \u03c3-bond is stronger due to greater overlap.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">55. A double bond contains:<\/mark><\/strong><br>A) 1 \u03c3 + 1 \u03c0<br>B) 2 \u03c3<br>C) 1 \u03c3 only<br>D) 2 \u03c0<br><strong>Answer: A<\/strong><br><strong>Explanation:<\/strong> Double bond = 1 sigma + 1 pi.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">56. A triple bond contains:<\/mark><\/strong><br>A) 1 \u03c3 + 1 \u03c0<br>B) 1 \u03c3 + 2 \u03c0<br>C) 2 \u03c3 + 1 \u03c0<br>D) 3 \u03c3<br><strong>Answer: B<\/strong><br><strong>Explanation:<\/strong> Triple bond = 1 sigma + 2 pi.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">57. In Molecular Orbital Theory (MOT), molecular orbitals are formed by:<\/mark><\/strong><br>A) Mixing of nuclei<br>B) Mixing of atomic orbitals<br>C) Overlap of sigma bonds<br>D) Overlap of pi bonds<br><strong>Answer: B<\/strong><br><strong>Explanation:<\/strong> MOT states molecular orbitals are linear combinations of atomic orbitals (LCAO).<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">58. Which is true for bonding molecular orbital (BMO)?<\/mark><\/strong><br>A) Higher energy than atomic orbital<br>B) Lower energy than atomic orbital<br>C) Destabilising<br>D) Anti-symmetric<br><strong>Answer: B<\/strong><br><strong>Explanation:<\/strong> BMO has lower energy than atomic orbitals \u2192 stabilising.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">59. Which is true for antibonding molecular orbital?<\/mark><\/strong><br>A) Higher energy<br>B) Lower energy<br>C) Stabilising<br>D) Increases bond order<br><strong>Answer: A<\/strong><br><strong>Explanation: <\/strong>Antibonding orbitals have higher energy \u2192 destabilising.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">60. Bond order (MOT) =<\/mark><\/strong><br>A) \u00bd (Nb \u2013 Na)<br>B) \u00bd (Na \u2013 Nb)<br>C) Nb + Na<br>D) Nb \/ Na<br><strong>Answer: A<\/strong><br><strong>Explanation:<\/strong> Bond order = \u00bd (no. of bonding electrons \u2013 no. of antibonding electrons).<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">61. In H\u2082 molecule, bond order is:<\/mark><\/strong><br>A) 0<br>B) 1<br>C) 2<br>D) 3<br><strong>Answer: B<\/strong><br><strong>Explanation: <\/strong>H\u2082 \u2192 2 bonding e\u207b, 0 antibonding e\u207b \u2192 (2\u20130)\/2 = 1.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">62. In He\u2082 molecule, bond order is:<\/mark><\/strong><br>A) 0<br>B) 1<br>C) 2<br>D) 3<br><strong>Answer: A<\/strong><br><strong>Explanation: <\/strong>He\u2082 \u2192 2 bonding e\u207b, 2 antibonding e\u207b \u2192 (2\u20132)\/2 = 0 (unstable).<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">63. Bond order of O\u2082 molecule is:<\/mark><\/strong><br>A) 1<br>B) 2<br>C) 3<br>D) 2.5<br><strong>Answer: B<\/strong><br><strong>Explanation: <\/strong>O\u2082 \u2192 bond order = 2 (paramagnetic).<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">64. O\u2082 molecule is:<\/mark><\/strong><br>A) Diamagnetic<br>B) Paramagnetic<br>C) Ferromagnetic<br>D) None<br><strong>Answer: B<\/strong><br><strong>Explanation: <\/strong>O\u2082 has 2 unpaired electrons in \u03c0 orbitals \u2192 paramagnetic.*<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">65. Bond order of O\u2082\u207a is:<\/mark><\/strong><br>A) 1.5<br>B) 2<br>C) 2.5<br>D) 3<br><strong>Answer: C<\/strong><br><strong>Explanation: <\/strong>O\u2082\u207a \u2192 one electron removed from antibonding \u2192 bond order 2.5.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">66. Bond order of O\u2082\u207b is:<\/mark><\/strong><br>A) 1.5<br>B) 2<br>C) 2.5<br>D) 3<br><strong>Answer: A<\/strong><br><strong>Explanation:<\/strong> O\u2082\u207b \u2192 one electron added to antibonding orbital \u2192 bond order 1.5.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">67. Which is diamagnetic?<\/mark><\/strong><br>A) O\u2082<br>B) O\u2082\u207a<br>C) O\u2082\u00b2\u207b<br>D) B\u2082<br><strong>Answer: C<\/strong><br><strong>Explanation: <\/strong>O\u2082\u00b2\u207b has paired electrons \u2192 diamagnetic.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">68. Bond order of N\u2082 is:<\/mark><\/strong><br>A) 1<br>B) 2<br>C) 3<br>D) 4<br><strong>Answer: C<\/strong><br><strong>Explanation: <\/strong>N\u2082 bond order = 3 (triple bond, very stable).<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">69. Bond order of N\u2082\u207a is:<\/mark><\/strong><br>A) 2<br>B) 2.5<br>C) 3<br>D) 3.5<br><strong>Answer: B<\/strong><br><strong>Explanation: <\/strong>N\u2082\u207a loses one electron from bonding orbital \u2192 bond order 2.5.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">70. Which molecule is paramagnetic according to MOT?<\/mark><\/strong><br>A) N\u2082<br>B) O\u2082<br>C) CO\u2082<br>D) H\u2082O<br><strong>Answer: B<\/strong><br><strong>Explanation:<\/strong> O\u2082 is paramagnetic (2 unpaired electrons).<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">71. The increasing bond order in O\u2082 species is:<\/mark><\/strong><br>A) O\u2082 &lt; O\u2082\u207a &lt; O\u2082\u00b2\u207b<br>B) O\u2082\u00b2\u207b &lt; O\u2082 &lt; O\u2082\u207a<br>C) O\u2082 &lt; O\u2082\u00b2\u207b &lt; O\u2082\u207a<br>D) O\u2082\u207a &lt; O\u2082 &lt; O\u2082\u00b2\u207b<br><strong>Answer: B<\/strong><br><strong>Explanation: <\/strong>Bond order: O\u2082\u00b2\u207b (1) &lt; O\u2082 (2) &lt; O\u2082\u207a (2.5).<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">72. According to MOT, which species is least stable?<\/mark><\/strong><br>A) N\u2082<br>B) O\u2082<br>C) He\u2082<br>D) CO<br><strong>Answer: C<\/strong><br><strong>Explanation:<\/strong> He\u2082 bond order = 0 \u2192 unstable.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">73. In B\u2082 molecule, magnetic property is:<\/mark><\/strong><br>A) Diamagnetic<br>B) Paramagnetic<br>C) Ferromagnetic<br>D) None<br><strong>Answer: B<\/strong><br>Explanation: B\u2082 has 2 unpaired electrons in \u03c0 orbitals \u2192 paramagnetic.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">74. CO molecule is isoelectronic with:<\/mark><\/strong><br>A) N\u2082<br>B) O\u2082<br>C) F\u2082<br>D) Ne\u2082<br><strong>Answer: A<\/strong><br><strong>Explanation:<\/strong><em> <\/em>CO (14 e\u207b) is isoelectronic with N\u2082 (14 e\u207b).<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">75. Which has highest bond energy?<\/mark><\/strong><br>A) O\u2082<br>B) N\u2082<br>C) F\u2082<br>D) Cl\u2082<br><strong>Answer: B<\/strong><br><strong>Explanation: <\/strong>N\u2082 has bond order 3 (triple bond) \u2192 highest bond energy.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">76. Resonance in molecules occurs due to:<\/mark><\/strong><br>A) Rapid interconversion of isomers<br>B) Delocalization of electrons<br>C) Vibrations of nuclei<br>D) Hybridization of orbitals<br><strong>Answer:<\/strong> B<br><strong>Explanation:<\/strong> Resonance represents electron delocalization across different positions without actual movement of atoms.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">77. The resonance energy of benzene is approximately:<\/mark><\/strong><br>A) 36 kcal\/mol<br>B) 50 kcal\/mol<br>C) 100 kcal\/mol<br>D) 10 kcal\/mol<br><strong>Answer:<\/strong> A<br><strong>Explanation:<\/strong> Benzene is more stable than expected due to resonance energy (~36 kcal\/mol).<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">78. Which ion shows resonance?<\/mark><\/strong><br>A) NH\u2084\u207a<br>B) CO\u2083\u00b2\u207b<br>C) Na\u207a<br>D) Cl\u207b<br><strong>Answer:<\/strong> B<br><strong>Explanation:<\/strong> Carbonate ion has delocalized \u03c0-electrons across three oxygen atoms.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">79. The most stable resonance structure is the one with:<\/mark><\/strong><br>A) Maximum number of covalent bonds<br>B) Least formal charge<br>C) Negative charge on more electronegative atom<br>D) All of the above<br><strong>Answer:<\/strong> D<br><strong>Explanation:<\/strong> Stability depends on bond maximization, proper charge placement, and minimal separation.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">80. In resonance, the actual structure of a molecule is:<\/mark><\/strong><br>A) One of the resonance forms<br>B) A mixture of resonance forms<br>C) An intermediate hybrid<br>D) Rapidly interchanging isomers<br><strong>Answer:<\/strong> C<br><strong>Explanation:<\/strong> The real structure is a resonance hybrid, more stable than any single canonical form.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">81. Which of the following molecules has resonance?<\/mark><\/strong><br>A) SO\u2082<br>B) NH\u2083<br>C) H\u2082O<br>D) CH\u2084<br><strong>Answer:<\/strong> A<br><strong>Explanation:<\/strong> SO\u2082 has multiple resonance structures with delocalized \u03c0-bonds.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">82. Hydrogen bonding is strongest in:<\/mark><\/strong><br>A) H\u2082S<br>B) H\u2082Se<br>C) H\u2082O<br>D) H\u2082Te<br><strong>Answer:<\/strong> C<br><strong>Explanation:<\/strong> Due to high electronegativity and small size of oxygen, H\u2082O shows strong H-bonding.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">83. Hydrogen bonding leads to:<\/mark><\/strong><br>A) Higher boiling points<br>B) Higher viscosity<br>C) Higher surface tension<br>D) All of the above<br><strong>Answer:<\/strong> D<br><strong>Explanation:<\/strong> H-bonding creates strong intermolecular forces, increasing these physical properties.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">84. Which of the following exhibits intramolecular hydrogen bonding?<\/mark><\/strong><br>A) o-nitrophenol<br>B) p-nitrophenol<br>C) m-nitrophenol<br>D) Phenol<br><strong>Answer:<\/strong> A<br><strong>Explanation:<\/strong> o-Nitrophenol has intramolecular H-bonding between \u2013OH and \u2013NO\u2082 group.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">85. Which of the following exhibits intermolecular hydrogen bonding?<\/mark><\/strong><br>A) o-nitrophenol<br>B) p-nitrophenol<br>C) Both A and B<br>D) None<br><strong>Answer:<\/strong> B<br><strong>Explanation:<\/strong> p-Nitrophenol molecules form H-bonds with neighboring molecules.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">86. Ice floats on water due to:<\/mark><\/strong><br>A) Lower density of ice because of H-bonding<br>B) Higher density of ice because of H-bonding<br>C) Presence of covalent bonds<br>D) Resonance in H\u2082O<br><strong>Answer:<\/strong> A<br><strong>Explanation:<\/strong> H-bonding in ice creates an open lattice structure, lowering density.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">87. Which of the following molecules shows resonance stabilization?<\/mark><\/strong><br>A) CH\u2082=CH\u2082<br>B) CH\u2083\u2013CH\u2083<br>C) C\u2086H\u2086<br>D) CH\u2084<br><strong>Answer:<\/strong> C<br><strong>Explanation:<\/strong> Benzene has delocalized \u03c0-electrons and resonance stabilization.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">88. Which type of hydrogen bond is stronger?<\/mark><\/strong><br>A) Intermolecular<br>B) Intramolecular<br>C) Both equal<br>D) None<br><strong>Answer:<\/strong> A<br><strong>Explanation:<\/strong> Intermolecular H-bonds generally lead to higher stability and stronger interactions.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">89. Which factor is not essential for hydrogen bonding?<\/mark><\/strong><br>A) High electronegativity<br>B) Small size of atom<br>C) Presence of lone pairs<br>D) High atomic mass<br><strong>Answer:<\/strong> D<br><strong>Explanation:<\/strong> Atomic mass doesn\u2019t influence hydrogen bonding; electronegativity and size do.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">90. Which of the following shows hydrogen bonding in liquid state?<\/mark><\/strong><br>A) HF<br>B) NH\u2083<br>C) H\u2082O<br>D) All of these<br><strong>Answer:<\/strong> D<br><strong>Explanation:<\/strong> HF, NH\u2083, and H\u2082O all form intermolecular hydrogen bonds in liquid state.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">91. The abnormal high boiling point of water is due to:<\/mark><\/strong><br>A) Ionic bonding<br>B) Covalent bonding<br>C) Hydrogen bonding<br>D) van der Waals forces<br><strong>Answer:<\/strong> C<br><strong>Explanation:<\/strong> Strong hydrogen bonds between water molecules increase its boiling point.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">92. Which of the following molecules does not show resonance?<\/mark><\/strong><br>A) O\u2083<br>B) NO\u2082\u207b<br>C) H\u2082O<br>D) CO\u2083\u00b2\u207b<br><strong>Answer:<\/strong> C<br><strong>Explanation:<\/strong> Water has localized bonds, no delocalization of electrons.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">93. Which of the following molecules shows extensive hydrogen bonding leading to dimer formation?<\/mark><\/strong><br>A) Acetic acid<br>B) Methanol<br>C) Phenol<br>D) Ammonia<br><strong>Answer:<\/strong> A<br><strong>Explanation:<\/strong> Acetic acid forms strong dimeric structures via intermolecular H-bonds.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">94. Hydrogen bonding is absent in:<\/mark><\/strong><br>A) HCl<br>B) HF<br>C) NH\u2083<br>D) H\u2082O<br><strong>Answer:<\/strong> A<br><strong>Explanation:<\/strong> Chlorine is large and less electronegative, so HCl does not form H-bonds.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">95. Which of the following explains the planarity of benzene?<\/mark><\/strong><br>A) Hybridization<br>B) Resonance<br>C) Hydrogen bonding<br>D) Ionic nature<br><strong>Answer:<\/strong> B<br><strong>Explanation:<\/strong> Delocalized \u03c0-electrons in resonance enforce planarity in benzene.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">96. Which bond order indicates resonance stabilization?<\/mark><\/strong><br>A) 1<br>B) 1.33<br>C) 2<br>D) 3<br><strong>Answer:<\/strong> B<br><strong>Explanation:<\/strong> Bond orders like 1.33 (e.g., CO\u2083\u00b2\u207b, NO\u2083\u207b) arise due to resonance.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">97. The anomalous high viscosity of glycerol is due to:<\/mark><\/strong><br>A) Ionic bonding<br>B) Extensive hydrogen bonding<br>C) Resonance<br>D) van der Waals forces<br><strong>Answer:<\/strong> B<br><strong>Explanation:<\/strong> Glycerol has three \u2013OH groups, forming multiple H-bonds \u2192 high viscosity.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">98. The bond angle in water decreases from tetrahedral angle due to:<\/mark><\/strong><br>A) Resonance<br>B) Lone pair\u2013bond pair repulsion and H-bonding<br>C) Hydrogen bonding only<br>D) Ionic bonding<br><strong>Answer:<\/strong> B<br><strong>Explanation:<\/strong> Strong lone pair repulsions reduce bond angle to ~104.5\u00b0.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\"><strong>99. Which of the following molecules exhibits both resonance and hydrogen bonding?<\/strong><\/mark><br>A) Benzene<br>B) Acetic acid<br>C) Methane<br>D) Ethylene<br><strong>Answer:<\/strong> B<br><strong>Explanation:<\/strong> Acetic acid has resonance in \u2013COOH and hydrogen bonding between molecules.<\/p>\n\n\n\n<p class=\"has-large-font-size\"><strong><mark style=\"background-color:rgba(0, 0, 0, 0)\" class=\"has-inline-color has-luminous-vivid-orange-color\">100. Which property of DNA structure is due to hydrogen bonding?<\/mark><\/strong><br>A) Double helix stability<br>B) Base pairing specificity<br>C) Complementary strand binding<br>D) All of the above<br><strong>Answer:<\/strong> D<br><strong>Explanation:<\/strong> H-bonding between bases stabilizes double helix and ensures specific base pairing.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>1. Which type of bond is formed by transfer of electrons?A) Ionic bondB) Covalent bondC) Metallic bondD) Hydrogen bondAnswer: AExplanation: Ionic bonds form due to complete transfer of electrons from one atom to another. 2. Ionic bond is generally formed between:A) Metal &amp; Non-metalB) Metal &amp; MetalC) Non-metal &amp; Non-metalD) Noble gasesAnswer: AExplanation: Metals lose<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[9],"tags":[15924,15926,15922,15915,10966,15886,15892,15876,15898,15901,15887,15899,15879,15883,15928,15914,15916,15884,15918,15921,15919,4029,15897,5649,5623,15923,15913,15927,15920,15900,15896,15894,15917,15925],"class_list":{"0":"post-12756","1":"post","2":"type-post","3":"status-publish","4":"format-standard","6":"category-chemistry","7":"tag-bond-energy","8":"tag-bond-length","9":"tag-chemical-bonding","10":"tag-chemical-bonding-problems","11":"tag-chemical-bonding-top-100-mcqs-with-answer-and-explanation","12":"tag-chemistry-formulas","13":"tag-chemistry-learning","14":"tag-chemistry-mcqs","15":"tag-chemistry-preparation-material","16":"tag-chemistry-questions-and-answers","17":"tag-chemistry-quiz","18":"tag-chemistry-revision","19":"tag-chemistry-study-material","20":"tag-competitive-exam-chemistry","21":"tag-covalent-bond","22":"tag-covalent-compounds","23":"tag-hybridization","24":"tag-intermolecular-forces","25":"tag-ionic-bond","26":"tag-ionic-compounds","27":"tag-lewis-structure","28":"tag-mcqs-adda","29":"tag-mcqs-for-chemistry-exam","30":"tag-mcqs-for-pc-psi-sda-fda-pdo-vao-banking-kas-ias-ssc-gd-ssc-chsl-ssc-cgl-for-all-compitative-exams","31":"tag-mcqs-for-sda-fda-pdo-vao-banking-kas-ias-ssc-gd-ssc-chsl-ssc-cgl-for-all-compitative-exams","32":"tag-metallic-bond","33":"tag-molecular-geometry","34":"tag-molecular-structure","35":"tag-polar-and-nonpolar-bonds","36":"tag-psc-chemistry-mcqs","37":"tag-ssc-chemistry-mcqs","38":"tag-upsc-chemistry-mcqs","39":"tag-valence-electrons","40":"tag-vsepr-theory"},"_links":{"self":[{"href":"https:\/\/mcqsadda.com\/index.php\/wp-json\/wp\/v2\/posts\/12756","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/mcqsadda.com\/index.php\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/mcqsadda.com\/index.php\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/mcqsadda.com\/index.php\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/mcqsadda.com\/index.php\/wp-json\/wp\/v2\/comments?post=12756"}],"version-history":[{"count":7,"href":"https:\/\/mcqsadda.com\/index.php\/wp-json\/wp\/v2\/posts\/12756\/revisions"}],"predecessor-version":[{"id":12925,"href":"https:\/\/mcqsadda.com\/index.php\/wp-json\/wp\/v2\/posts\/12756\/revisions\/12925"}],"wp:attachment":[{"href":"https:\/\/mcqsadda.com\/index.php\/wp-json\/wp\/v2\/media?parent=12756"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/mcqsadda.com\/index.php\/wp-json\/wp\/v2\/categories?post=12756"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/mcqsadda.com\/index.php\/wp-json\/wp\/v2\/tags?post=12756"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}