McMurry9e PPT CH01

John E.
McMurry
www.cengage.com/chemistry/mcmurry
Chapter 1
Structure and Bonding
2016 Cengage Learning. All Rights Reserved.
Learning Objectives
(1.1)
Atomic structure: The nucleus
(1.2)
Atomic structure: Orbitals
(1.3)
Atomic structure: Electron configurations
(1.4)
Development of chemical bonding theory
Learning Objectives
(1.5)
Describing chemical bonds: Valence bond
theory
(1.6)
sp3 hybrid orbitals and the structure of methane
(1.7)
sp3 hybrid orbitals and the structure of ethane
(1.8)
sp2 hybrid orbitals and the structure of ethylene
Learning Objectives
(1.9)
sp hybrid orbitals and the structure of acetylene
(1.10)
Hybridization of nitrogen, oxygen, phosphorus,
and sulfur
(1.11)
Describing chemical bonds: Molecular orbital
theory
(1.12)
Drawing chemical structures
What is Organic Chemistry?

Living things
are made of
organic
chemicals
Proteins that
make up hair
DNA
Foods and
medicines
Origins of Organic Chemistry

Foundations date from mid-1700s
Compounds obtained from plants and animals
Low-melting solids
Hard to isolate, purify, and work with
Organic compounds were considered to have
some vital force as they were from living

sources
Thought that it could not be synthesized in

laboratory
Origins of Organic Chemistry

1816, Chevreul found that soap can be
separated into several organic compounds

which he termed fatty acids
1828, Whler showed that it was possible to
convert inorganic salt ammonium cyanate into

organic substance urea
Organic Chemistry
Study of carbon compounds
More than 50 million known chemical
compounds contain carbon

Carbon is a group 4A element
Can share 4 valence electrons and form 4

covalent bonds
Able to bond with one another to form long
chains and rings
Only element that has the ability to form
immense diversity of compounds
Figure 1.1 - The Position of

Carbon in the Periodic Table
Atomic Structure - The Nucleus

Positively charged
Surrounded by a cloud of negatively charged
electrons (at a distance of 10-10 m)
Consist of subatomic particles
Protons, positively charged

Neutrons, electrically neutral
Atomic Structure - The Nucleus

Diameter of an atom is about 210-10 m
200 picometers (pm) [the unit ngstrm () is
10-10 m = 100 pm]
Atomic Number and Atomic

Mass
Atomic number (Z) - Number of protons in an
atom's nucleus
Mass number (A) - Number of protons plus
neutrons
Atoms of a given element have the same atomic
number
Isotopes: Atoms with the same atomic number
but different mass numbers
Atomic mass (atomic weight) - Weighted
average mass in atomic mass units (amu) of an
elements naturally occurring isotopes
Atomic Structure - Orbitals

Wave equation - Mathematical equation which
describes the behavior of a specific electron in

an atom
Wave function, or orbital, is the solution of wave

equation
Denoted by the Greek letter psi ()
Plot of 2 describes where an electron is most
likely to be
An electron cloud has no specific boundary
Most probable area is considered


s, p, d, and f are different kinds of orbitals
s and p orbitals are common in organic and
biological chemistry
s orbitals - Spherical, nucleus at center
p orbitals - Dumbbell-shaped, nucleus at middle
d orbitals - Elongated dumbbell-shaped, nucleus
at center

Orbitals in an atom are organized into different
electron shells
Centered around the nucleus in shells of

increasing size and energy
Different shells contain different numbers and
kinds of orbitals
Each orbital can be occupied by two electrons
Figure 1.4 - The Energy Levels of

Electrons in an Atom
P-Orbitals
Each shell consists of three mutually
perpendicular p orbitals
Denoted px, py, and pz
Node: Region of zero electron density

Separates two lobes of each p orbital
Atomic Structure: Electron

Configurations
Ground-state electron configuration: Listing
of orbitals occupied by an atoms electrons
Called lowest-energy arrangement
Rules
Lowest-energy orbitals fill first, in the order of 1s
2s 2p 3s 3p 4s 3d
Aufbau principle
Atomic Structure: Electron

Configurations
Electrons act as if they were spinning around an
axis
Spin can have only two orientations, up () and

down ()
Only two electrons can occupy an orbital, and
they must be of opposite spin
Pauli exclusion principle
If two or more empty orbitals of equal energy
are available, electrons occupy each with

parallel spins until all orbitals have one electron
Hund's rule
Worked Example
Give the ground-state electron configuration for
sulfur
Solution:
Atomic number of sulfur is 16
Number of electrons = 16
In a more concise way it can
be written as
1s2 2s2 2p6 3s2 3p4
Worked Example
How many electrons does magnesium have in
its outermost electron shell?

Solution:
Elements of the periodic table are organized into

groups based on the number of outer-shell
electrons each element has
Using the periodic table we locate the group of
the element, magnesium
Magnesium - Group 2A
Has two electrons in its outermost shell
Development of Chemical
Bonding Theory
Kekul and Couper independently observed that
carbon is tetravalent
Jacobus Van't Hoff and Le Bel proposed that the
four bonds of carbon have specific spatial
directions
Atoms surround carbon at corners of a regular

tetrahedron
Figure 1.6 - A Representation of a

Tetrahedral Carbon Atom
Bonding Theory
Atoms form bonds because the resulting
compound is more stable than the separate

atoms
Valence shell: Atoms outermost shell
Impart special stability to the noble gas elements
Ionic bonds - Ions held together by a
electrostatic attraction
Formed as a result of electron transfers
Covalent bond: Formed by sharing of electrons

Organic compounds have covalent bonds from
sharing electrons
Bonding Theory
Molecule: Neutral collection of atoms held
together by covalent bonds

Electron-dot structures: Represents valence
shell electrons of an atom as dots
Called Lewis structures
Line-bond structures: Indicates two-electron
covalent bond as a line drawn between atoms
Called Kekul structures
Bonding Theory
Bonding Theory
Number of covalent bonds an atom forms
depends on the number of additional valence

electrons it needs to reach a stable octet
Carbon has four valence electrons (2s2 2p2),
forming four bonds
Nitrogen has five valence electrons (2s2 2p3),
forming three bonds
Non-Bonding Electrons
Lone pair - Valence electrons not used in
bonding
Example
Nitrogen atom in ammonia (NH3)
Shares six valence electrons in three covalent bonds

Two valence electrons are nonbonding lone pair
Worked Example
Draw a molecule of chloroform, CHCl3, using
solid, wedged, and dashed lines to show its

tetrahedral geometry
Solution:
Valence Bond Theory

Covalent bond forms when two atoms approach
each other closely so that a singly occupied

orbital on one atom overlaps a singly occupied
orbital on the other atom
HH bond results from the overlap of two singly

occupied hydrogen 1s orbitals
HH bond is cylindrically symmetrical, sigma ()
bond
Valence Bond Theory

Reaction 2 H H2 releases 436 kJ/mol
HH has a bond strength of 436 kJ/mol
(1 kJ = 0.2390 kcal; 1 kcal = 4.184 kJ)
Valence Bond Theory

Bond length: Ideal distance between nuclei that
leads to maximum stability
If too close, they repel

If too far apart, bonding is weak
sp3 Orbitals and the Structure of

Methane
Carbon has 4 valence electrons (2s2 2p2)
In CH4, all CH bonds are identical (tetrahedral)
sp3 hybrid orbitals: s orbital and three p
orbitals combine to form four equivalent,

unsymmetrical, tetrahedrally oriented orbitals

Methane
sp3 orbitals in a C atom overlap with 1s orbitals
of an H atom to form four identical CH bonds

Each CH bond has a strength of 439 kJ/mol
and a length of 109 pm
Bond angle: Formed between two adjacent
bonds

Ethane
Two Cs bond to each other by overlap of an
sp3 orbital from each

Three sp3 orbitals on each C overlap with H 1s
orbitals to form six CH bonds
CH bond strength in ethane is 421 kJ/mol

CC bond is 154 pm long and strength is 377
kJ/mol
Bond angles of ethane are tetrahedral
Figure 1.12 - The Structure

of Ethane
Worked Example
Draw a line-bond structure for propane,
CH3CH2CH3
Predict the value of each bond angle, and

indicate the overall shape of the molecule
Solution:
Geometry - Tetrahedral
Bond angles - 109(approximately)

Ethylene
sp2 hybrid orbitals: Derived by combination of
an s atomic orbital with two p atomic orbitals

sp2 orbitals are in a plane with an angle of
120from each other
Remaining p orbital is perpendicular to the plane

Ethylene
Two sp2 hybridized orbitals overlap to form a
bond
p orbitals interact by sideways overlap to form a
pi () bond
sp2sp2 bond and 2p2p bond result in
sharing four electrons and formation of CC
double bond
Electrons in the bond are centered between
nuclei
Electrons in the bond occupy regions on either
side of a line between nuclei
Structure of Ethylene
H atoms form s bonds with four sp2 orbitals
HCH and HCC form bond angles of about
120
CC double bond in ethylene is shorter and
stronger than single bond in ethane
Worked Example
Draw electron-dot and line-bond structures of
formaldehyde
Indicate the hybridization of the carbon orbitals
Solution:
Two hydrogens, one carbon, and one oxygen can
combine in one way
The orbitals are sp2-hybridized

sp Orbitals and the Structure of

Acetylene
Carbon can form a triple bond sharing six
electrons
Carbon 2s orbital hybridizes with a single p
orbital giving two sp hybrids
Two p orbitals remain unchanged
sp orbitals are linear, 180apart on x-axis

Two p orbitals are perpendicular on the y-axis
and the z-axis
Figure 1.15 - sp Hybridization
Orbitals of Acetylene
Two sp hybrid orbitals from each C form
sp
sp bond
pz orbitals from each C form a pzpz bond by
sideways overlap
py orbitals overlap to form pypy bond
Bonding in Acetylene
Sharing of six electrons forms CC
Two sp orbitals form bonds with hydrogens
Shortest and strongest carboncarbon bond
Table 1.2 - Comparison of CC and CH Bonds

in Methane, Ethane, Ethylene, and Acetylene
Worked Example
Draw a line-bond structure for propyne,
CH3CCH
Indicate the hybridization of the orbitals on each

carbon
Predict a value for each bond angle
Solution:
Worked Example
C3-H bonds are bonds
Overlap of an sp3 orbital of carbon
3 with s orbital of hydrogen
C1-H bond is a bond
Overlap of an sp orbital of carbon

1 with an s orbital of hydrogen
C2-C3 bond is a bond

Overlap of an sp orbital of carbon
2 with an sp3 orbital of carbon 3
Three C1-C2 bonds
Worked Example
Bond angle
Between three carbon atoms is 180
HC1C2 is 180
Between hydrogen and the sp3-hybridized carbon
is 109
Hybridization of Nitrogen, Oxygen,

Phosphorus, and Sulfur
HNH bond angle in methylamine 107.1
CNH bond angle is 110.3
Ns orbitals hybridize to form four sp3 orbitals
One sp3 orbital is occupied by two nonbonding
electrons, and three sp3 orbitals have one

electron each

Oxygen atom in methanol can be described as
sp3-hybridized
COH bond angle in methanol is 108.5
Two sp3 hybrid orbitals on oxygen are occupied
by nonbonding electron lone pairs

Methyl phosphate, CH3OPO32 OPO bond angle is approximately 110 to
112
Implies sp3 hybridization in the phosphorus

orbitals

Dimethyl sulfide [(CH3)2S] is the simplest
example of a sulfide
Described by approximate sp3 hybridization
around sulfur
Have significant deviation from the tetrahedral
angle
Worked Example
Identify all nonbonding lone pairs of electrons in
the oxygen atom in dimethyl ether, CH3OCH3
What is its expected geometry
Solution:
The sp3-hybridized oxygen atom has tetrahedral
geometry
Molecular Orbital (MO) Theory

Description of covalent bond formation as
resulting from a mathematical combination of

atomic orbitals to form molecular orbitals
Bonding MO: Molecular orbital that is lower in
energy than the atomic orbitals from which it is
formed
Antibonding MO: Molecular orbital that is
higher in energy than the atomic orbitals from
which it is formed
Figure 1.17 - Molecular Orbitals

of H2
Molecular Orbital Theory

The bonding MO is from combining p orbital
lobes with the same algebraic sign

The antibonding MO is from combining lobes
with opposite signs
Only bonding MO is occupied
Drawing Chemical Structures

Several shorthand methods have been
developed to write structures

Condensed structures: C-H or C-C single
bonds are not shown, they are understood
Example
Rules for Drawing Skeletal

Structures
Carbon atoms arent usually shown
Carbon atom is assumed to be at each
intersection of two lines (bonds) and at the end

of each line
Hydrogen atoms bonded to carbon arent shown
Atoms other than carbon and hydrogen are
shown
Table 1.3 - Kekul and Skeletal

Structures for Some Compounds
Worked Example
How many hydrogens are bonded to each
carbon in the following compound
Give the molecular formula of each substance
Worked Example
Solution:
Summary
Organic chemistry - Study of carbon compounds
Atom: Charged nucleus containing positively
charged protons and neutrally charged neutrons

surrounded by negatively charged electrons
Electronic structure of an atom is described by
wave equation
Different orbitals have different energy levels and

different shapes
s orbitals are spherical, p orbitals are dumbbellshaped
Summary
Covalent bonds - Electron pair is shared
between atoms
Valence bond theory - Electron sharing occurs
by the overlapping of two atomic orbitals
Molecular orbital (MO) theory - Bonds result
from combination of atomic orbitals to give
molecular orbitals, which belong to the entire
molecule
Summary
Sigma () bonds - Circular cross-section and
are formed by head-on interaction

Pi () bonds - Formed by sideways interaction of
p orbitals
Carbon uses hybrid orbitals to form bonds in
organic molecules
In single bonds with tetrahedral geometry, carbon

has four sp3 hybrid orbitals
In double bonds with planar geometry, carbon
uses three equivalent sp2 hybrid orbitals and one
unhybridized p orbital
Summary
Carbon uses two equivalent sp hybrid orbitals to

form a triple bond with linear geometry, with two
unhybridized p orbitals
Atoms such as nitrogen and oxygen hybridize to
form strong, oriented bonds
Nitrogen atom in ammonia and the oxygen atom

in water are sp3-hybridized
Structures in which carboncarbon and carbon
hydrogen bonds arent shown are called

condensed structures

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John E.

2016 Cengage Learning. All Rights Reserved.

2016 Cengage Learning. All Rights Reserved.

What is Organic Chemistry?

2016 Cengage Learning. All Rights Reserved.

Origins of Organic Chemistry

some vital force as they were from living

Thought that it could not be synthesized in

2016 Cengage Learning. All Rights Reserved.

Origins of Organic Chemistry

separated into several organic compounds

1828, Whler showed that it was possible to

convert inorganic salt ammonium cyanate into

2016 Cengage Learning. All Rights Reserved.

compounds contain carbon

Can share 4 valence electrons and form 4

2016 Cengage Learning. All Rights Reserved.

Figure 1.1 - The Position of

2016 Cengage Learning. All Rights Reserved.

Atomic Structure - The Nucleus

Protons, positively charged

2016 Cengage Learning. All Rights Reserved.

Atomic Structure - The Nucleus

2016 Cengage Learning. All Rights Reserved.

Atomic Number and Atomic

Atomic Structure - Orbitals

describes the behavior of a specific electron in

Wave function, or orbital, is the solution of wave

Plot of 2 describes where an electron is most

Most probable area is considered

Atomic Structure - Orbitals

2016 Cengage Learning. All Rights Reserved.

Atomic Structure - Orbitals

Centered around the nucleus in shells of

Different shells contain different numbers and

2016 Cengage Learning. All Rights Reserved.

Figure 1.4 - The Energy Levels of

2016 Cengage Learning. All Rights Reserved.

Denoted px, py, and pz

Node: Region of zero electron density

2016 Cengage Learning. All Rights Reserved.

Atomic Structure: Electron

of orbitals occupied by an atoms electrons

Called lowest-energy arrangement

2016 Cengage Learning. All Rights Reserved.

Atomic Structure: Electron

Spin can have only two orientations, up () and

Pauli exclusion principle

If two or more empty orbitals of equal energy

are available, electrons occupy each with

Atomic number of sulfur is 16

2016 Cengage Learning. All Rights Reserved.

its outermost electron shell?

Elements of the periodic table are organized into

Has two electrons in its outermost shell

2016 Cengage Learning. All Rights Reserved.

Atoms surround carbon at corners of a regular

2016 Cengage Learning. All Rights Reserved.

Figure 1.6 - A Representation of a