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Chapter 8 “Covalent Bonding”
Section 8.1 Molecular Compounds ,[object Object],[object Object]
Section 8.1 Molecular Compounds ,[object Object],[object Object]
Bonds are… ,[object Object],[object Object],[object Object]
Covalent Bonds ,[object Object],[object Object]
Molecules ,[object Object],[object Object],[object Object],[object Object]
How does H 2  form? ,[object Object],(diatomic hydrogen molecule) + + + +
How does H 2  form? ,[object Object],[object Object],+ +
Covalent bonds ,[object Object],[object Object],[object Object],[object Object],[object Object]
Covalent bonding ,[object Object],F
Covalent bonding ,[object Object],[object Object],F F F F F F F
Covalent bonding ,[object Object],[object Object],[object Object],F F
Covalent bonding ,[object Object],[object Object],[object Object],F F
Covalent bonding ,[object Object],[object Object],[object Object],F F
Covalent bonding ,[object Object],[object Object],[object Object],F F
Covalent bonding ,[object Object],[object Object],[object Object],F F
Covalent bonding ,[object Object],[object Object],[object Object],[object Object],F F
Covalent bonding ,[object Object],[object Object],[object Object],[object Object],F F 8 Valence electrons
Covalent bonding ,[object Object],[object Object],[object Object],[object Object],F F 8 Valence electrons
 
Molecular Compounds ,[object Object],[object Object]
Molecular Compounds ,[object Object],[object Object],[object Object],[object Object]
Molecular Compounds ,[object Object],[object Object],[object Object]
- Page 215 These are some of the different ways to represent ammonia: 1. The  molecular formula  shows how many atoms of each element are present 2. The  structural formula  ALSO shows the arrangement of these atoms! 3. The  ball and stick  model is the  BEST , because it shows a 3-dimensional arrangement.
Section 8.2 The Nature of Covalent Bonding ,[object Object],[object Object]
Section 8.2 The Nature of Covalent Bonding ,[object Object],[object Object]
Section 8.2 The Nature of Covalent Bonding ,[object Object],[object Object]
Section 8.2 The Nature of Covalent Bonding ,[object Object],[object Object]
Section 8.2 The Nature of Covalent Bonding ,[object Object],[object Object]
A Single Covalent Bond is... ,[object Object],[object Object],[object Object],[object Object],[object Object]
Sodium Chloride Crystal Lattice ,[object Object]
How to show the formation… ,[object Object],[object Object],[object Object],[object Object],[object Object]
Water ,[object Object],[object Object],[object Object],[object Object],[object Object],H O
Water ,[object Object],[object Object],[object Object],H O
Water ,[object Object],[object Object],H H Note the two “ unshared ” pairs of electrons O
[object Object],[object Object],[object Object]
Multiple Bonds ,[object Object],[object Object],[object Object],[object Object],[object Object]
Dot diagram for Carbon dioxide ,[object Object],[object Object],[object Object],[object Object],[object Object],C O
Carbon dioxide ,[object Object],C O
Carbon dioxide ,[object Object],C O O
Carbon dioxide ,[object Object],C O O
Carbon dioxide ,[object Object],C O O
Carbon dioxide ,[object Object],C O O
Carbon dioxide ,[object Object],C O O
Carbon dioxide ,[object Object],C O O
Carbon dioxide ,[object Object],O C O
Carbon dioxide ,[object Object],[object Object],[object Object],O C O
Carbon dioxide ,[object Object],[object Object],[object Object],O C O 8 valence electrons
Carbon dioxide ,[object Object],[object Object],[object Object],O C O 8 valence electrons
Carbon dioxide ,[object Object],[object Object],[object Object],O C O 8 valence electrons
How to draw them? ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Example ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],N H
Examples ,[object Object],[object Object],[object Object],N H H H
Example: HCN ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
HCN ,[object Object],[object Object],[object Object],N H C
HCN ,[object Object],[object Object],[object Object],[object Object],N H C
HCN ,[object Object],[object Object],[object Object],[object Object],[object Object],N H C
Another way of indicating bonds ,[object Object],[object Object],[object Object],H H O = H H O
Other Structural Examples H   C N C  O H H
A Coordinate Covalent Bond... ,[object Object],[object Object],Both the carbon and oxygen give another single electron to share O C
Coordinate Covalent Bond ,[object Object],[object Object],O C Oxygen gives  both  of these electrons, since it has no more singles to share. This carbon electron moves to make a pair with the other single.
Coordinate Covalent Bond ,[object Object],[object Object],O C C  O The coordinate covalent bond is shown with an arrow as:
Coordinate covalent bond ,[object Object],[object Object],[object Object],[object Object]
Bond Dissociation Energies... ,[object Object],[object Object]
Resonance is... ,[object Object],[object Object],[object Object],[object Object],[object Object]
Resonance in Ozone Neither   structure is correct, it is actually a hybrid of the two.  To show it, draw all varieties possible, and join them with a double-headed arrow. Note the  different location  of the  double bond
Resonance ,[object Object],[object Object],[object Object]
Polyatomic ions  – note the different positions of the double bond. Resonance in a carbonate ion (CO 3 2- ): Resonance in an acetate ion (C 2 H 3 O 2 1- ):
The  3 Exceptions  to Octet rule ,[object Object],[object Object],[object Object],[object Object]
Exceptions to Octet rule ,[object Object],[object Object],[object Object],[object Object]
Section 8.3 Bonding Theories ,[object Object],[object Object]
Section 8.3 Bonding Theories ,[object Object],[object Object]
Molecular Orbitals are... ,[object Object],[object Object],[object Object]
Molecular Orbitals - definitions ,[object Object],[object Object],[object Object]
- Pages 230 and 231 Sigma bond  is symmetrical along the axis between the two nuclei. Pi bond  is above and below the bond axis, and is weaker than sigma
VSEPR: stands for... ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
VSEPR ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
VSEPR for methane (a gas): ,[object Object],[object Object],[object Object],C H H H H This 2-dimensional drawing does not show a true representation of the chemical arrangement.
4 atoms bonded ,[object Object],[object Object],[object Object],C H H H H 109.5º
Other angles, pages 232 - 233 ,[object Object],[object Object],[object Object],[object Object]
- Page 232 Methane has an angle of 109.5 o , called  tetrahedral Ammonia has an angle of 107 o , called  pyramidal Note the unshared pair that is repulsion for other electrons.
Section 8.4 Polar Bonds and Molecules ,[object Object],[object Object]
Section 8.4 Polar Bonds and Molecules ,[object Object],[object Object]
Section 8.4 Polar Bonds and Molecules ,[object Object],[object Object]
Section 8.4 Polar Bonds and Molecules ,[object Object],[object Object]
Bond Polarity ,[object Object],[object Object],[object Object],[object Object]
Bond Polarity ,[object Object],[object Object],[object Object]
Electronegativity? ,[object Object],Linus Pauling 1901 - 1994
Table of Electronegativities Higher electronegativity
Bond Polarity ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Bond Polarity ,[object Object],[object Object],[object Object],[object Object],       and    
Bond Polarity ,[object Object],[object Object],[object Object],H Cl
Polar molecules ,[object Object],[object Object],[object Object],[object Object],[object Object]
Polar molecules ,[object Object],[object Object]
Polar molecules ,[object Object],[object Object]
Polar molecules ,[object Object],[object Object]
Attractions between molecules ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
#2. Dipole interactions ,[object Object],[object Object],[object Object],[object Object]
#2. Dipole interactions ,[object Object],[object Object],[object Object],H F     H F    
#2. Dipole Interactions                                                
#3. Hydrogen bonding ,[object Object],[object Object],[object Object],[object Object]
Order of Intermolecular attraction strengths ,[object Object],[object Object],[object Object],[object Object]
#3. Hydrogen bonding defined: ,[object Object],[object Object],[object Object]
Hydrogen Bonding (Shown in water) This hydrogen is bonded covalently to: 1) the highly negative oxygen, and 2) a nearby unshared pair. H H O  +  -  + H H O  +  -  +
Hydrogen bonding allows H 2 O to be a liquid at room conditions. H H O H H O H H O H H O H H O H H O H H O
Attractions and properties ,[object Object],[object Object],[object Object],[object Object]
Attractions and properties ,[object Object],[object Object],[object Object],[object Object]
Covalent Network Compounds Some covalently bonded substances DO NOT form discrete molecules. Diamond, a network of covalently bonded carbon atoms Graphite, a network of covalently bonded carbon atoms
End of Chapter 8

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Chemistry - Chp 8 - Covalent Bonding - PowerPoint

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  • 24. - Page 215 These are some of the different ways to represent ammonia: 1. The molecular formula shows how many atoms of each element are present 2. The structural formula ALSO shows the arrangement of these atoms! 3. The ball and stick model is the BEST , because it shows a 3-dimensional arrangement.
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  • 59. Other Structural Examples H C N C O H H
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  • 66. Resonance in Ozone Neither structure is correct, it is actually a hybrid of the two. To show it, draw all varieties possible, and join them with a double-headed arrow. Note the different location of the double bond
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  • 68. Polyatomic ions – note the different positions of the double bond. Resonance in a carbonate ion (CO 3 2- ): Resonance in an acetate ion (C 2 H 3 O 2 1- ):
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  • 75. - Pages 230 and 231 Sigma bond is symmetrical along the axis between the two nuclei. Pi bond is above and below the bond axis, and is weaker than sigma
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  • 81. - Page 232 Methane has an angle of 109.5 o , called tetrahedral Ammonia has an angle of 107 o , called pyramidal Note the unshared pair that is repulsion for other electrons.
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  • 89. Table of Electronegativities Higher electronegativity
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  • 100. #2. Dipole Interactions                                
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  • 104. Hydrogen Bonding (Shown in water) This hydrogen is bonded covalently to: 1) the highly negative oxygen, and 2) a nearby unshared pair. H H O  +  -  + H H O  +  -  +
  • 105. Hydrogen bonding allows H 2 O to be a liquid at room conditions. H H O H H O H H O H H O H H O H H O H H O
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  • 108. Covalent Network Compounds Some covalently bonded substances DO NOT form discrete molecules. Diamond, a network of covalently bonded carbon atoms Graphite, a network of covalently bonded carbon atoms