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Chemical Bonding Part-2
Chemical Bonding Part-2
CHEMICAL BONDING
Ionic Bond, Co-valent Bond, Co-ordinate Bond, Fajan's rule
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Hydrogen Bond
7. Hydrogen Bond : Identify the case where hydrogen bonding is possible
(i) H 2 O( g ) (ii) NH 3 () (iii) CH 3 O CH 3 (iv) C6 H 5 OH (v) NH2 OH
(vi) CCl3 COOH (vii) C 6 H 5 O CH 3 (viii) C6 H 5 CH 2 OH
OH OH OH CH 2 OH
NO 2 CH 3 OH
(ix) (x) (xi) (xii)
OH
8. Select the molecule separatly showing inter/intra or both hydrogen bonding OH
CH 3
(i) CH 2 OH (ii) CH 2 OH (iii) HO CH 2 CH 2 OD (iv) D C OH (v)
CH 3
CH 2 OH (CH 2 ) 2
OH
CH 2 OH
OH
OH OH
(vi) (vii) (viii) (ix) CH 3 (x)
CH 3
NH 2 OH H OH H OH
COOH H OH HO H
CH 3 CH 3
9. Arrange the following in decreasing order :
CH 3
(c) OH (d) CH 2 CH 2 OH (Boiling point)
OH OH OH CH 3
OH
(iv) (a) , (b) , (c) , (d) (Decreasing order of boiling point)
OH CH 3
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10. Answer the following : by using the concept of hydrogen bonding.
(i) C 2 H 5 OH is soluble in water while CH 3 O CH 3 is not.
(ii) H2 O2 is liquid while NH3 is gas at 25oC and 1 atm.
(iii) In KHF2, hydrogen bond is formed as F .....H F .
NO 2
(vii) Sugar is soluble in water and toluene.
(viii) Order of viscocity is Glycerol >Glycol > water.
(ix) NH3 can be liquified easily by applying pressure while PH3 not.
CH 3
O CH 3 CH 2 OH OH
(x) is less soluble in water than OR
Hybridisation
11. Select the correct and incorrect statements regarding the hybridisation.
(i) Hybridisation is a real phenomenon.
(ii) In hybridisation, hybrid orbitals are always equivalent.
(iii) In hybridisation same no. of hybrid orbitals are obtained as mixed initially.
(iv) Any type of orbital (Half filled, full filled or blank) can participate in hybridisation.
(v) Promotion of electron(s) to other sub-orbit of high energy and mixing of orbitals requires energy.
(vi) Only half filled hybridised orbital can participate in bonding.
(vii) Fully filled and fully vacant orbital can also participate in bonding.
(viii) Hybridised orbitals overlap more efficiently to form stronger bonds.
(ix) In hybridisation orbitals of two same or different elements are mixed.
(x) Different facts like bond angle, bond length variation can be explained on the basis of hybridisation.
12. Find the hybridisation of central atom
(i) PCl 3 (iii) PCl 5 (iii) NH 4 BrF5
(iv) (v) XeF2 (vi) CO2
(vii) NO
2
(viii) N 2O (ix) NO
2
(x) NO 3 (xi) CO3 (xii) BO 3
(xiii) H 3 O (xiv) ClO 3 (xv) SO
3 (xvi) ClO 4 (xvii) PO 4 (xviii) HCN
(xix) H 2 O 2 (xx) N 2 O 3 (xxi) HNO3 (xxii) SO 2 (xxiii) SO3 (xxiv)H 2SO 3
(xxv) H 2SO 4 (xxvi) H 3 PO 4 (xxvii) SO 2 Cl 2 (xxviii) HIO 3 (xxix) BF3 (xxx) ClF3
(xxxi) XeF4 (xxxii) BrCl5 (xxxiii) SF6 (xxxiv) XeF6 (xxxv) I F7
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Br Br Br Br F
Br OH
(vi) , , , (vii) (Showing different dipole moment than expected)
Br
Br
F C C C
CH 3 C C
(viii) (Showing different dipole moment than expected) (ix) , ,
C C C C
C C
Molecular Orbital Theory
15. Select the T/F statements regarding the MOT.
(i) Orbital used in MOT is common to all the atoms involved in bond formaton.
(ii) In MOT orbitals of different atoms are mixed to give same number of molecular orbitals.
(iii) In MOT orbitals of same atom are mixed to give same number of molecular orbital.
(iv) The energy of B.O is less as compared to orbitals mixed initally.
(v) The energy of A.B.O is more as compared to orbitals mixed initially.
(vi) B.O present nearest to the nucleus of atom involved in molecule formation.
(vii) A.B.O present nearest to the nucleus of atoms involved in molecule formation.
(viii) Bond strength increases as bond order increases.
(ix) Bond length increases as bond order decreases.
(x) Species containing unpaired electron(s) are diamagnetic in nature.
16. Find the bond order of following species.
(i) H2 (ii) H 2 (iii) H 2 (iv) He2 (v) He 2 (vi) N 2
(vii) N 2 (viii) O 2 (ix) O 2 (x) O 2 (xi) NO (xii) NO (xiii) C2
(xiv) C 2 (xv) C 2 (xvi) CO (xvii) CO (xviii) C 2 (xix) NO
(xx) C N (xxi) Ne2 (xxii) F2
17. Arrange the following as instructed
(a) H 2 , He 2 , N 2 , N 2 (Decreasing bond strength) (b) O 2 , O 2 , O 2 , O 2 (Decreasing bond length)
(c) N 2 , N 2 , N 2 , N 2 (Decreasing stability order) (d) NO, NO , CO, CO (Decreasing bond order)
18. Select the paramagnetic /Diamagnetic species.
(i) H2 (ii) N 2 (iii) C2 (iv) H 2 (v) O 2 (vi) C 2
(vii) H 2 (viii) O 2 (ix) C 2 (x) He2 (xi) O 2 (xii) CO
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-----------------------------------ANSWER KEY----------------------------------------
1. (i) Metallic bond, (ii) Ionic bond, (iii) Co-valent /Co-ordinate (iv) Co-valent/Co-ordinate (v) Ionic bond
2. (i) F (ii) T (iii) F (iv) T (v) T (vi) F (vii) F (viii) F (ix) T (x) T
O O
3. (i) Na S Na (ii) K O S O K (iii) Ba [O S O]
O O
O O O
(iv) Cu [O S O] (v) 2K [O C O] (vi) K [O Cl O]
O O
S O O
(viii) K O P O K (ix) 3 Ca 2 [O P O ]
(vii) K O S O K
O OK O
O O O O O
(x) 2 Al 3 [O S O]
3
(xi) K O Cr O Cr O K (xii) K O S O O S O K
O O O O O
CN
CN CN NC CN
(xiii) K N C
(xiv) 4K Fe2 (xv) 2K Ni
CN CN NC CN
CN
O O
(xvi) Na O S S S S O Na
O O
4. (i) F (ii) T (iii) T (iv) T (v) T (vi) T (vii) T (viii) T
10. (i)T (ii) T (iii) T (iv) T (v) T (vi) T (vii) F (viii) T (ix) T (x) T
11. (i) F (ii) F (iii) T (iv) T (v) T (vi) F (vii) T (viii) T (ix) F (x) T
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12. (i) (sp3) (ii) (sp3d) (iii) (sp3) (iv) (sp3d2) (v) (sp3d1) (vi) (sp)
(vii) (sp 2 ) (viii) (sp) (ix) (sp) (x) (sp 2 ) (xi) (sp 2 ) (xii) (sp 2 )
(xiii) (sp 3 ) (xiv) (sp 3 ) (xv) (sp 3 ) (xvi) (sp 3 ) (xvii) (sp 3 ) (xviii) (sp)
(xix) (sp 3 ) (xx) (sp 2 ) (xxi) (sp 2 ) (xxii) (sp 2 ) (xxiii) (sp 2 ) (xxiv) (sp 3 )
(xxv) (sp 3 ) (xxvi) (sp 3 ) (xxvii) (sp 3 ) (xxviii) (sp 3 ) (xxix) (sp 2 ) (xxx) (sp3d1)
(xxxi) (sp3d2) (xxxii) (sp3d2) (xxxiii) (sp3d2) (xxxiv) (sp3d3) (xxxv) (sp3d3)
13. (i) (V -shape) (ii) (Pyramidal) (iii) (Linear) (iv) (T-shape) (v) (Squar planer)
(vi) (T-shape) (vii) (Pyramidal) (viii) (Sqare pyramidal) (ix) (Linear)
(x) (Square planer) (xi) Square pyramidal (xii) (Sea-saw)
(xiii) (Pentagonal bipyramidal) (xiv) (Tetrahedral) (xv) Trigonal bipyramidal
(xvi) Octahedral (xvii) Square planer
14. (i) a > b (ii) a = b = c (iii) a > b > c >d (iv) da cb
(v) cdba (vi) abdc (vii) Due to hydrogen bonding
(viii) Steric repulsion (ix) a b c' ( Zero)
15. (i) T (ii) T (iii) F (iv) T (v) T (vi) T (vii) F (viii) T (ix) T (x) F
1 1 1
16. (i) 1 (ii) (iii) (iv) 0 (v) (vi) 2.5 (vii) 2.5 (viii) 1.5 (ix) 2.5 (x) 1 (xi) 2.5
2 2 2
(xii) 3 (xiii) 2 (xiv) 2.5 (xv) 3 (xvi) 3 (xvii) 2.5 (xviii) 2.5 (xix) 2.5 (xx) 2.5 (xxi) 0 (xxii) 1.5
17. (a) N 2 N H 2 He
2 2
(b) O O2 O O
2 2 2
(c) N 2 N 2 N 2 N 2 (d) CO NO NO CO
18. Paramagnetic - ii, iv, v, vi, vii, viii, x, xiii, xiv, xv, xvi, xviii , Diamagnetic - i, iii, ix, xi, xii, xvii
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