(thermodynamics) a thermodynamic quantity equal to the internal energy of a system plus the product of its volume and pressure
As the number of shared electrons increases, the bond length shortens
(see table 8.5)
C. Bond Energy and Enthalpy (using bond energy to calculate approximate
energies for rxns)
1.
Q1 and Q2 are numerical ion charges
c. r = distance between ion center in nanometers
d. negative sign indicates an attractive force
C. Bond Length (covalent)
1.
the charge on an ion is equal to a constant charge e multiplied by an integer from 1 to 15
Formulas for compounds are balanced so that the total positive ionic
charge is equal to the total negative ionic charge
Al O
2
3
3
2
+ -
Total positive = +6
Total negative = -6
C. Sizes of Ions
1.
not equal or interchangeable in value, quantity, or significance
If nonequivalent Lewis structures exist for a species, those with the
formal charges closest to zero, and with negative formal charges on
the most electronegative atoms are considered the best candidates
2.
Non-bonding and bonding electron pairs will be as far apart as possible
Arrangement of Electron Pairs Around an Atom Yielding Minimum
Repulsion
# of Electron
Pairs
Shape Arrangement of Electron Pairs
2 Linear
Arrange the remaining atoms to satisfy the duet rule for
hydrogen and the octet rule for the second row elements
8.11 Exceptions to the Octet Rule
A. Boron Trifluoride
1.
Energy change is exothermic (negative sign)
Example: Formation of lithium fluoride
Process Description Energy Change (kJ)
Li(s) ‡ Li(g) Sublimation energy 161
Li(g) ‡ Li
+
(g) + e
-
Ionization energy 520
1/2F2 ‡ F(g) Bond energy (1/2 mole) 77
F(g) + e
-
‡ F
-
(g) Electron affinity -328
Li
+
(g) + F
-
(g) ‡ LiF(s) Lattice energy -1047
Li(s) + 1/2F2(g) ‡ LiF(s) DH -617
3.
If nonequivalent Lewis structures exist for a species, those with the
formal charges closest to zero, and with negative formal charges on
the most electronegative atoms are considered the best candidates
2.
of or relating to a molecule made up of more than two atoms
Percent ionic character is difficult to calculate for compounds
containing polyatomic ions8.7 The Covalent Chemical Bond: A Model
A. Strengths of the Bond Model
1.
any of the monovalent metals of group I of the periodic table (lithium or sodium or potassium or rubidium or cesium or francium)
The lattice formed by alkali metals and halogens (1:1 ratio) is cubic
except for cesium salts
B. Lattice Energy Calculations
1.
ø
ö
è
æ
=
r
Q Q
Lattice Energy k
1 2
a. k = a proportionality constant dependent on the solid structure
and the electron configuration
b.
a metric unit of length equal to one billionth of a meter
Q1 and Q2 are numerical ion charges
c. r = distance between ion center in nanometers
d. negative sign indicates an attractive force
C. Bond Length (covalent)
1.
Non-bonding and bonding electron pairs will be as far apart as possible
Arrangement of Electron Pairs Around an Atom Yielding Minimum
Repulsion
# of Electron
Pairs
Shape Arrangement of Electron Pairs
2 Linear
United States civil rights leader who was elected to the legislature in Georgia but was barred from taking his seat because he opposed the Vietnam War (born 1940)
AP Chemistry
A. Allan
Chapter 8 Notes - Bonding: General Concepts
8.1 Types of Chemical Bonds
A. Ionic Bonding
1.
Q1 and Q2 are numerical ion charges
c. r = distance between ion center in nanometers
d. negative sign indicates an attractive force
C. Bond Length (covalent)
1.
The lattice formed by alkali metals and halogens (1:1 ratio) is cubic
except for cesium salts
B. Lattice Energy Calculations
1.
ø
ö
è
æ
=
r
Q Q
Lattice Energy k
1 2
a. k = a proportionality constant dependent on the solid structure
and the electron configuration
b.
Bonds can not adequately explain some phenomena
a. resonance
8.8 Covalent Bond Energies and Chemical Reactions
A. Average Bond Energies
Process Energy Required (kJ/mol)
CH4(g) ‡ CH3(g) + H(g) 435
CH3(g) ‡ CH2(g) + H(g) 453
CH2(g) ‡ CH(g) + H(g) 425
CH(g) ‡ C(g) + H(g) 339
Total 1652
Average 413
B. Multiple Bonds
1.
any of five related nonmetallic elements (fluorine or chlorine or bromine or iodine or astatine) that are all monovalent and readily form negative ions
The lattice formed by alkali metals and halogens (1:1 ratio) is cubic
except for cesium salts
B. Lattice Energy Calculations
1.
ø
ö
è
æ
=
r
Q Q
Lattice Energy k
1 2
a. k = a proportionality constant dependent on the solid structure
and the electron configuration
b.
harmonious arrangement or relation of parts or elements within a whole (as in a design)
The lattice formed by alkali metals and halogens (1:1 ratio) is cubic
except for cesium salts
B. Lattice Energy Calculations
1.
ø
ö
è
æ
=
r
Q Q
Lattice Energy k
1 2
a. k = a proportionality constant dependent on the solid structure
and the electron configuration
b.
Energy change is exothermic (negative sign)
Example: Formation of lithium fluoride
Process Description Energy Change (kJ)
Li(s) ‡ Li(g) Sublimation energy 161
Li(g) ‡ Li
+
(g) + e
-
Ionization energy 520
1/2F2 ‡ F(g) Bond energy (1/2 mole) 77
F(g) + e
-
‡ F
-
(g) Electron affinity -328
Li
+
(g) + F
-
(g) ‡ LiF(s) Lattice energy -1047
Li(s) + 1/2F2(g) ‡ LiF(s) DH -617
3.
an abundant tasteless odorless multivalent nonmetallic element; best known in yellow crystals; occurs in many sulphide and sulphate minerals and even in native form (especially in volcanic regions)
Boron often forms molecules that obey the octet
rule
B. Sulfur Hexafluoride
1.
a process in which substances are changed into others
Bonds can not adequately explain some phenomena
a. resonance
8.8 Covalent Bond Energies and Chemical Reactions
A. Average Bond Energies
Process Energy Required (kJ/mol)
CH4(g) ‡ CH3(g) + H(g) 435
CH3(g) ‡ CH2(g) + H(g) 453
CH2(g) ‡ CH(g) + H(g) 425
CH(g) ‡ C(g) + H(g) 339
Total 1652
Average 413
B. Multiple Bonds
1.
a soft silver-white univalent element of the alkali metal group; the lightest metal known; occurs in several minerals
Energy change is exothermic (negative sign)
Example: Formation of lithium fluoride
Process Description Energy Change (kJ)
Li(s) ‡ Li(g) Sublimation energy 161
Li(g) ‡ Li
+
(g) + e
-
Ionization energy 520
1/2F2 ‡ F(g) Bond energy (1/2 mole) 77
F(g) + e
-
‡ F
-
(g) Electron affinity -328
Li
+
(g) + F
-
(g) ‡ LiF(s) Lattice energy -1047
Li(s) + 1/2F2(g) ‡ LiF(s) DH -617
3.
the molecular weight of a substance expressed in grams
Bonds can not adequately explain some phenomena
a. resonance
8.8 Covalent Bond Energies and Chemical Reactions
A. Average Bond Energies
Process Energy Required (kJ/mol)
CH4(g) ‡ CH3(g) + H(g) 435
CH3(g) ‡ CH2(g) + H(g) 453
CH2(g) ‡ CH(g) + H(g) 425
CH(g) ‡ C(g) + H(g) 339
Total 1652
Average 413
B. Multiple Bonds
1.
a change directly from the solid to the gaseous state
Energy change is exothermic (negative sign)
Example: Formation of lithium fluoride
Process Description Energy Change (kJ)
Li(s) ‡ Li(g) Sublimation energy 161
Li(g) ‡ Li
+
(g) + e
-
Ionization energy 520
1/2F2 ‡ F(g) Bond energy (1/2 mole) 77
F(g) + e
-
‡ F
-
(g) Electron affinity -328
Li
+
(g) + F
-
(g) ‡ LiF(s) Lattice energy -1047
Li(s) + 1/2F2(g) ‡ LiF(s) DH -617
3.
Energy change is exothermic (negative sign)
Example: Formation of lithium fluoride
Process Description Energy Change (kJ)
Li(s) ‡ Li(g) Sublimation energy 161
Li(g) ‡ Li
+
(g) + e
-
Ionization energy 520
1/2F2 ‡ F(g) Bond energy (1/2 mole) 77
F(g) + e
-
‡ F
-
(g) Electron affinity -328
Li
+
(g) + F
-
(g) ‡ LiF(s) Lattice energy -1047
Li(s) + 1/2F2(g) ‡ LiF(s) DH -617
3.
The lattice formed by alkali metals and halogens (1:1 ratio) is cubic
except for cesium salts
B. Lattice Energy Calculations
1.
ø
ö
è
æ
=
r
Q Q
Lattice Energy k
1 2
a. k = a proportionality constant dependent on the solid structure
and the electron configuration
b.
Lattice energy increases as the ionic charge increases and the
distance between anions and cations decreases
8.6 Partial Ionic Character of Covalent Bonds
A. Calculating Percent Ionic Character
x100%
calculated dipole moment of X Y
measured dipole moment of X Y
Percent ionic character
ø
ö
è
æ -
=
+ -
B. Ionic vs.
When necessary to exceed the octet rule for one of several third
row elements, assume that the extra electrons be placed on the
central atom
8.12 Resonance
A. Nitrate ion
1.
SF6 fills the 3s and 3p orbitals with 8 of the
valence electrons, and places the other 4 in the
higher energy 3d orbital
C. More About the Octet Rule
1.
a representation of something, often on a smaller scale
Percent ionic character is difficult to calculate for compounds
containing polyatomic ions8.7 The Covalent Chemical Bond: A Model
A. Strengths of the Bond Model
1.
Lone (unshared) electron pairs require more room than bonding pairs
(they have greater repulsive forces) and tend to compress the angles
between bonding pairs
3.
Bonds can not adequately explain some phenomena
a. resonance
8.8 Covalent Bond Energies and Chemical Reactions
A. Average Bond Energies
Process Energy Required (kJ/mol)
CH4(g) ‡ CH3(g) + H(g) 435
CH3(g) ‡ CH2(g) + H(g) 453
CH2(g) ‡ CH(g) + H(g) 425
CH(g) ‡ C(g) + H(g) 339
Total 1652
Average 413
B. Multiple Bonds
1.
characterized by denial or opposition or resistance
Q1 and Q2 are numerical ion charges
c. r = distance between ion center in nanometers
d. negative sign indicates an attractive force
C. Bond Length (covalent)
1.
Q1 and Q2 are numerical ion charges
c. r = distance between ion center in nanometers
d. negative sign indicates an attractive force
C. Bond Length (covalent)
1.
Energy change is exothermic (negative sign)
Example: Formation of lithium fluoride
Process Description Energy Change (kJ)
Li(s) ‡ Li(g) Sublimation energy 161
Li(g) ‡ Li
+
(g) + e
-
Ionization energy 520
1/2F2 ‡ F(g) Bond energy (1/2 mole) 77
F(g) + e
-
‡ F
-
(g) Electron affinity -328
Li
+
(g) + F
-
(g) ‡ LiF(s) Lattice energy -1047
Li(s) + 1/2F2(g) ‡ LiF(s) DH -617
3.
any of various water-soluble compounds capable of turning litmus blue and reacting with an acid to form a salt and water
The lattice formed by alkali metals and halogens (1:1 ratio) is cubic
except for cesium salts
B. Lattice Energy Calculations
1.
ø
ö
è
æ
=
r
Q Q
Lattice Energy k
1 2
a. k = a proportionality constant dependent on the solid structure
and the electron configuration
b.
"A molecule is composed of atoms that are bound together by sharing
pairs of electrons using the atomic orbitals of the bound atoms
D. Derivations of the Localized Model
1.
Only experimental evidence can conclusively determine the correct
bonding situation in a molecule
8.13 Molecular Structure: The VSEPR Model
A. Valence Shell Electron Pair Repulsion (VSEPR)
1.
Q1 and Q2 are numerical ion charges
c. r = distance between ion center in nanometers
d. negative sign indicates an attractive force
C. Bond Length (covalent)
1.
Description of the type of atomic orbitals used to share or hold lone
pairs of electrons
8.10 Lewis Structures
A. Electrons and Stability
1. "the most important requirement for the formation of a stable
compound is that the atoms achieve noble gas configurations
2.
"A molecule is composed of atoms that are bound together by sharing
pairs of electrons using the atomic orbitals of the bound atoms
D. Derivations of the Localized Model
1.
As the number of shared electrons increases, the bond length shortens
(see table 8.5)
C. Bond Energy and Enthalpy (using bond energy to calculate approximate
energies for rxns)
1.
As the number of shared electrons increases, the bond length shortens
(see table 8.5)
C. Bond Energy and Enthalpy (using bond energy to calculate approximate
energies for rxns)
1.
an arrangement of objects or people side by side in a line
Arrange the remaining atoms to satisfy the duet rule for
hydrogen and the octet rule for the second row elements
8.11 Exceptions to the Octet Rule
A. Boron Trifluoride
1.
"A molecule is composed of atoms that are bound together by sharing
pairs of electrons using the atomic orbitals of the bound atoms
D. Derivations of the Localized Model
1.
Bonds can not adequately explain some phenomena
a. resonance
8.8 Covalent Bond Energies and Chemical Reactions
A. Average Bond Energies
Process Energy Required (kJ/mol)
CH4(g) ‡ CH3(g) + H(g) 435
CH3(g) ‡ CH2(g) + H(g) 453
CH2(g) ‡ CH(g) + H(g) 425
CH(g) ‡ C(g) + H(g) 339
Total 1652
Average 413
B. Multiple Bonds
1.
Lattice energy increases as the ionic charge increases and the
distance between anions and cations decreases
8.6 Partial Ionic Character of Covalent Bonds
A. Calculating Percent Ionic Character
x100%
calculated dipole moment of X Y
measured dipole moment of X Y
Percent ionic character
ø
ö
è
æ -
=
+ -
B. Ionic vs.
Description of the type of atomic orbitals used to share or hold lone
pairs of electrons
8.10 Lewis Structures
A. Electrons and Stability
1. "the most important requirement for the formation of a stable
compound is that the atoms achieve noble gas configurations
2.
The lattice formed by alkali metals and halogens (1:1 ratio) is cubic
except for cesium salts
B. Lattice Energy Calculations
1.
ø
ö
è
æ
=
r
Q Q
Lattice Energy k
1 2
a. k = a proportionality constant dependent on the solid structure
and the electron configuration
b.
Energy change is exothermic (negative sign)
Example: Formation of lithium fluoride
Process Description Energy Change (kJ)
Li(s) ‡ Li(g) Sublimation energy 161
Li(g) ‡ Li
+
(g) + e
-
Ionization energy 520
1/2F2 ‡ F(g) Bond energy (1/2 mole) 77
F(g) + e
-
‡ F
-
(g) Electron affinity -328
Li
+
(g) + F
-
(g) ‡ LiF(s) Lattice energy -1047
Li(s) + 1/2F2(g) ‡ LiF(s) DH -617
3.
Arrange the remaining atoms to satisfy the duet rule for
hydrogen and the octet rule for the second row elements
8.11 Exceptions to the Octet Rule
A. Boron Trifluoride
1.
As the number of shared electrons increases, the bond length shortens
(see table 8.5)
C. Bond Energy and Enthalpy (using bond energy to calculate approximate
energies for rxns)
1.
Formulas for compounds are balanced so that the total positive ionic
charge is equal to the total negative ionic charge
Al O
2
3
3
2
+ -
Total positive = +6
Total negative = -6
C. Sizes of Ions
1.
"A molecule is composed of atoms that are bound together by sharing
pairs of electrons using the atomic orbitals of the bound atoms
D. Derivations of the Localized Model
1.
The lattice formed by alkali metals and halogens (1:1 ratio) is cubic
except for cesium salts
B. Lattice Energy Calculations
1.
ø
ö
è
æ
=
r
Q Q
Lattice Energy k
1 2
a. k = a proportionality constant dependent on the solid structure
and the electron configuration
b.
Q1 and Q2 are numerical ion charges
c. r = distance between ion center in nanometers
d. negative sign indicates an attractive force
C. Bond Length (covalent)
1.
If nonequivalent Lewis structures exist for a species, those with the
formal charges closest to zero, and with negative formal charges on
the most electronegative atoms are considered the best candidates
2.
Only experimental evidence can conclusively determine the correct
bonding situation in a molecule
8.13 Molecular Structure: The VSEPR Model
A. Valence Shell Electron Pair Repulsion (VSEPR)
1.
an intermediate scale value regarded as normal or usual
Bonds can not adequately explain some phenomena
a. resonance
8.8 Covalent Bond Energies and Chemical Reactions
A. Average Bond Energies
Process Energy Required (kJ/mol)
CH4(g) ‡ CH3(g) + H(g) 435
CH3(g) ‡ CH2(g) + H(g) 453
CH2(g) ‡ CH(g) + H(g) 425
CH(g) ‡ C(g) + H(g) 339
Total 1652
Average 413
B. Multiple Bonds
1.
determined by conditions or circumstances that follow
The lattice formed by alkali metals and halogens (1:1 ratio) is cubic
except for cesium salts
B. Lattice Energy Calculations
1.
ø
ö
è
æ
=
r
Q Q
Lattice Energy k
1 2
a. k = a proportionality constant dependent on the solid structure
and the electron configuration
b.
pleasing to the eye or mind as through beauty or charm
Q1 and Q2 are numerical ion charges
c. r = distance between ion center in nanometers
d. negative sign indicates an attractive force
C. Bond Length (covalent)
1.
the mathematical symbol 0 denoting absence of quantity
If nonequivalent Lewis structures exist for a species, those with the
formal charges closest to zero, and with negative formal charges on
the most electronegative atoms are considered the best candidates
2.
Bonds can not adequately explain some phenomena
a. resonance
8.8 Covalent Bond Energies and Chemical Reactions
A. Average Bond Energies
Process Energy Required (kJ/mol)
CH4(g) ‡ CH3(g) + H(g) 435
CH3(g) ‡ CH2(g) + H(g) 453
CH2(g) ‡ CH(g) + H(g) 425
CH(g) ‡ C(g) + H(g) 339
Total 1652
Average 413
B. Multiple Bonds
1.
relation with respect to comparative quantity or magnitude
The lattice formed by alkali metals and halogens (1:1 ratio) is cubic
except for cesium salts
B. Lattice Energy Calculations
1.
ø
ö
è
æ
=
r
Q Q
Lattice Energy k
1 2
a. k = a proportionality constant dependent on the solid structure
and the electron configuration
b.
Formulas for compounds are balanced so that the total positive ionic
charge is equal to the total negative ionic charge
Al O
2
3
3
2
+ -
Total positive = +6
Total negative = -6
C. Sizes of Ions
1.
Percent ionic character is difficult to calculate for compounds
containing polyatomic ions8.7 The Covalent Chemical Bond: A Model
A. Strengths of the Bond Model
1.
Non-bonding and bonding electron pairs will be as far apart as possible
Arrangement of Electron Pairs Around an Atom Yielding Minimum
Repulsion
# of Electron
Pairs
Shape Arrangement of Electron Pairs
2 Linear
the property created by the space between two objects
Q1 and Q2 are numerical ion charges
c. r = distance between ion center in nanometers
d. negative sign indicates an attractive force
C. Bond Length (covalent)
1.
Bonds can not adequately explain some phenomena
a. resonance
8.8 Covalent Bond Energies and Chemical Reactions
A. Average Bond Energies
Process Energy Required (kJ/mol)
CH4(g) ‡ CH3(g) + H(g) 435
CH3(g) ‡ CH2(g) + H(g) 453
CH2(g) ‡ CH(g) + H(g) 425
CH(g) ‡ C(g) + H(g) 339
Total 1652
Average 413
B. Multiple Bonds
1.
Lattice energy increases as the ionic charge increases and the
distance between anions and cations decreases
8.6 Partial Ionic Character of Covalent Bonds
A. Calculating Percent Ionic Character
x100%
calculated dipole moment of X Y
measured dipole moment of X Y
Percent ionic character
ø
ö
è
æ -
=
+ -
B. Ionic vs.
When a molecule exhibits resonance, ANY of the resonance structures
can be used to predict the molecular structure using the VSEPR model
D. Molecules Containing No Single Central Atom
1.
Q1 and Q2 are numerical ion charges
c. r = distance between ion center in nanometers
d. negative sign indicates an attractive force
C. Bond Length (covalent)
1.
Arrange the remaining atoms to satisfy the duet rule for
hydrogen and the octet rule for the second row elements
8.11 Exceptions to the Octet Rule
A. Boron Trifluoride
1.
having the same quantity, value, or measure as another
Formulas for compounds are balanced so that the total positive ionic
charge is equal to the total negative ionic charge
Al O
2
3
3
2
+ -
Total positive = +6
Total negative = -6
C. Sizes of Ions
1.
"A molecule is composed of atoms that are bound together by sharing
pairs of electrons using the atomic orbitals of the bound atoms
D. Derivations of the Localized Model
1.
The lattice formed by alkali metals and halogens (1:1 ratio) is cubic
except for cesium salts
B. Lattice Energy Calculations
1.
ø
ö
è
æ
=
r
Q Q
Lattice Energy k
1 2
a. k = a proportionality constant dependent on the solid structure
and the electron configuration
b.
Energy change is exothermic (negative sign)
Example: Formation of lithium fluoride
Process Description Energy Change (kJ)
Li(s) ‡ Li(g) Sublimation energy 161
Li(g) ‡ Li
+
(g) + e
-
Ionization energy 520
1/2F2 ‡ F(g) Bond energy (1/2 mole) 77
F(g) + e
-
‡ F
-
(g) Electron affinity -328
Li
+
(g) + F
-
(g) ‡ LiF(s) Lattice energy -1047
Li(s) + 1/2F2(g) ‡ LiF(s) DH -617
3.
influence that results in motion, stress, etc. when applied
Q1 and Q2 are numerical ion charges
c. r = distance between ion center in nanometers
d. negative sign indicates an attractive force
C. Bond Length (covalent)
1.
Lattice energy increases as the ionic charge increases and the
distance between anions and cations decreases
8.6 Partial Ionic Character of Covalent Bonds
A. Calculating Percent Ionic Character
x100%
calculated dipole moment of X Y
measured dipole moment of X Y
Percent ionic character
ø
ö
è
æ -
=
+ -
B. Ionic vs.
Bonds can not adequately explain some phenomena
a. resonance
8.8 Covalent Bond Energies and Chemical Reactions
A. Average Bond Energies
Process Energy Required (kJ/mol)
CH4(g) ‡ CH3(g) + H(g) 435
CH3(g) ‡ CH2(g) + H(g) 453
CH2(g) ‡ CH(g) + H(g) 425
CH(g) ‡ C(g) + H(g) 339
Total 1652
Average 413
B. Multiple Bonds
1.
Lattice energy increases as the ionic charge increases and the
distance between anions and cations decreases
8.6 Partial Ionic Character of Covalent Bonds
A. Calculating Percent Ionic Character
x100%
calculated dipole moment of X Y
measured dipole moment of X Y
Percent ionic character
ø
ö
è
æ -
=
+ -
B. Ionic vs.
Formulas for compounds are balanced so that the total positive ionic
charge is equal to the total negative ionic charge
Al O
2
3
3
2
+ -
Total positive = +6
Total negative = -6
C. Sizes of Ions
1.
Lattice energy increases as the ionic charge increases and the
distance between anions and cations decreases
8.6 Partial Ionic Character of Covalent Bonds
A. Calculating Percent Ionic Character
x100%
calculated dipole moment of X Y
measured dipole moment of X Y
Percent ionic character
ø
ö
è
æ -
=
+ -
B. Ionic vs.
have a disposition to do or be something; be inclined
Lone (unshared) electron pairs require more room than bonding pairs
(they have greater repulsive forces) and tend to compress the angles
between bonding pairs
3.
an area that is in the middle of some larger region
Q1 and Q2 are numerical ion charges
c. r = distance between ion center in nanometers
d. negative sign indicates an attractive force
C. Bond Length (covalent)
1.
Description of the type of atomic orbitals used to share or hold lone
pairs of electrons
8.10 Lewis Structures
A. Electrons and Stability
1. "the most important requirement for the formation of a stable
compound is that the atoms achieve noble gas configurations
2.
harmonious arrangement or relation of parts within a whole
Formulas for compounds are balanced so that the total positive ionic
charge is equal to the total negative ionic charge
Al O
2
3
3
2
+ -
Total positive = +6
Total negative = -6
C. Sizes of Ions
1.
When necessary to exceed the octet rule for one of several third
row elements, assume that the extra electrons be placed on the
central atom
8.12 Resonance
A. Nitrate ion
1.
When necessary to exceed the octet rule for one of several third
row elements, assume that the extra electrons be placed on the
central atom
8.12 Resonance
A. Nitrate ion
1.
If nonequivalent Lewis structures exist for a species, those with the
formal charges closest to zero, and with negative formal charges on
the most electronegative atoms are considered the best candidates
2.
a particular course of action intended to achieve a result
Energy change is exothermic (negative sign)
Example: Formation of lithium fluoride
Process Description Energy Change (kJ)
Li(s) ‡ Li(g) Sublimation energy 161
Li(g) ‡ Li
+
(g) + e
-
Ionization energy 520
1/2F2 ‡ F(g) Bond energy (1/2 mole) 77
F(g) + e
-
‡ F
-
(g) Electron affinity -328
Li
+
(g) + F
-
(g) ‡ LiF(s) Lattice energy -1047
Li(s) + 1/2F2(g) ‡ LiF(s) DH -617
3.
white crystalline form of especially sodium chloride used to season and preserve food
The lattice formed by alkali metals and halogens (1:1 ratio) is cubic
except for cesium salts
B. Lattice Energy Calculations
1.
ø
ö
è
æ
=
r
Q Q
Lattice Energy k
1 2
a. k = a proportionality constant dependent on the solid structure
and the electron configuration
b.
Bonds can not adequately explain some phenomena
a. resonance
8.8 Covalent Bond Energies and Chemical Reactions
A. Average Bond Energies
Process Energy Required (kJ/mol)
CH4(g) ‡ CH3(g) + H(g) 435
CH3(g) ‡ CH2(g) + H(g) 453
CH2(g) ‡ CH(g) + H(g) 425
CH(g) ‡ C(g) + H(g) 339
Total 1652
Average 413
B. Multiple Bonds
1.
Arrange the remaining atoms to satisfy the duet rule for
hydrogen and the octet rule for the second row elements
8.11 Exceptions to the Octet Rule
A. Boron Trifluoride
1.
a visible clue that something has happened or is present
Q1 and Q2 are numerical ion charges
c. r = distance between ion center in nanometers
d. negative sign indicates an attractive force
C. Bond Length (covalent)
1.
Non-bonding and bonding electron pairs will be as far apart as possible
Arrangement of Electron Pairs Around an Atom Yielding Minimum
Repulsion
# of Electron
Pairs
Shape Arrangement of Electron Pairs
2 Linear
The lattice formed by alkali metals and halogens (1:1 ratio) is cubic
except for cesium salts
B. Lattice Energy Calculations
1.
ø
ö
è
æ
=
r
Q Q
Lattice Energy k
1 2
a. k = a proportionality constant dependent on the solid structure
and the electron configuration
b.
free from error; especially conforming to fact or truth
Only experimental evidence can conclusively determine the correct
bonding situation in a molecule
8.13 Molecular Structure: The VSEPR Model
A. Valence Shell Electron Pair Repulsion (VSEPR)
1.
If nonequivalent Lewis structures exist for a species, those with the
formal charges closest to zero, and with negative formal charges on
the most electronegative atoms are considered the best candidates
2.
coming next after the first in position in space or time
Arrange the remaining atoms to satisfy the duet rule for
hydrogen and the octet rule for the second row elements
8.11 Exceptions to the Octet Rule
A. Boron Trifluoride
1.
Arrange the remaining atoms to satisfy the duet rule for
hydrogen and the octet rule for the second row elements
8.11 Exceptions to the Octet Rule
A. Boron Trifluoride
1.
Non-bonding and bonding electron pairs will be as far apart as possible
Arrangement of Electron Pairs Around an Atom Yielding Minimum
Repulsion
# of Electron
Pairs
Shape Arrangement of Electron Pairs
2 Linear
Arrange the remaining atoms to satisfy the duet rule for
hydrogen and the octet rule for the second row elements
8.11 Exceptions to the Octet Rule
A. Boron Trifluoride
1.
"A molecule is composed of atoms that are bound together by sharing
pairs of electrons using the atomic orbitals of the bound atoms
D. Derivations of the Localized Model
1.
English statesman who opposed Henry VIII's divorce from Catherine of Aragon and was imprisoned and beheaded; recalled for his concept of Utopia, the ideal state
SF6 fills the 3s and 3p orbitals with 8 of the
valence electrons, and places the other 4 in the
higher energy 3d orbital
C. More About the Octet Rule
1.
the linear extent in space from one end to the other
Q1 and Q2 are numerical ion charges
c. r = distance between ion center in nanometers
d. negative sign indicates an attractive force
C. Bond Length (covalent)
1.
uninterrupted in time and indefinitely long continuing
The lattice formed by alkali metals and halogens (1:1 ratio) is cubic
except for cesium salts
B. Lattice Energy Calculations
1.
ø
ö
è
æ
=
r
Q Q
Lattice Energy k
1 2
a. k = a proportionality constant dependent on the solid structure
and the electron configuration
b.
SF6 fills the 3s and 3p orbitals with 8 of the
valence electrons, and places the other 4 in the
higher energy 3d orbital
C. More About the Octet Rule
1.
When necessary to exceed the octet rule for one of several third
row elements, assume that the extra electrons be placed on the
central atom
8.12 Resonance
A. Nitrate ion
1.
Bonds can not adequately explain some phenomena
a. resonance
8.8 Covalent Bond Energies and Chemical Reactions
A. Average Bond Energies
Process Energy Required (kJ/mol)
CH4(g) ‡ CH3(g) + H(g) 435
CH3(g) ‡ CH2(g) + H(g) 453
CH2(g) ‡ CH(g) + H(g) 425
CH(g) ‡ C(g) + H(g) 339
Total 1652
Average 413
B. Multiple Bonds
1.
Description of the type of atomic orbitals used to share or hold lone
pairs of electrons
8.10 Lewis Structures
A. Electrons and Stability
1. "the most important requirement for the formation of a stable
compound is that the atoms achieve noble gas configurations
2.
Lattice energy increases as the ionic charge increases and the
distance between anions and cations decreases
8.6 Partial Ionic Character of Covalent Bonds
A. Calculating Percent Ionic Character
x100%
calculated dipole moment of X Y
measured dipole moment of X Y
Percent ionic character
ø
ö
è
æ -
=
+ -
B. Ionic vs.
If nonequivalent Lewis structures exist for a species, those with the
formal charges closest to zero, and with negative formal charges on
the most electronegative atoms are considered the best candidates
2.
Only experimental evidence can conclusively determine the correct
bonding situation in a molecule
8.13 Molecular Structure: The VSEPR Model
A. Valence Shell Electron Pair Repulsion (VSEPR)
1.
Created on Tue Jan 10 23:32:49 EST 2012
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