chapter 6 -chemical bonding a steroid alkaloid derived from skin secretions of the phyllobates and...

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Chapter 6 -Chemical Chapter 6 -Chemical Bonding Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison-arrow frogs. It is one of the most potent venoms known. Batrachotoxin

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Page 1: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Chapter 6 -Chemical BondingChapter 6 -Chemical Bonding

A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison-arrow frogs. It is one of the most potent venoms known.

Batrachotoxin

Page 2: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

BondsBonds Forces that hold groups of atoms together and Forces that hold groups of atoms together and

make them function as a unit.make them function as a unit.

Ionic bonds– transfer of electronsIonic bonds– transfer of electrons

Covalent bonds– sharing of electronsCovalent bonds– sharing of electrons

Polar Covalent bonds – unequal sharing of electrons Polar Covalent bonds – unequal sharing of electrons that results in an that results in an unbalanced unbalanced distribution of chargedistribution of charge

Page 3: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

ElectronegativityElectronegativity The ability of an atom in a molecule The ability of an atom in a molecule

to attract shared electrons to to attract shared electrons to itself.itself.

Linus Pauling1901 - 1994

e-e-

Page 4: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Table of Electronegativities

Page 5: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow
Page 6: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Shielding Effect

• Electrons in the inner energy levels block the attraction of the nucleus for the valence electrons.

• Shielding increases down a group.

• This causes EN values to decrease.

Page 7: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

What is Nuclear Shielding?

P+

P+P+

P+

P+

P+P+

P+

P+

e-

e-

e-

The nucleus (+) pulls the electron (-) close to the core.

The further the electron is away from the nucleus, the weaker the nuclear pull.

e-

Inner electrons shield outer electrons from the nuclear pull.

Page 8: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Range of EN Values

3.3 2.0 0.5 0

Polar covalent- Electrons are shared, but unequally. There is some degree of ionic character

in these bonds.

Mostly Ionic Polar Covalent Mostly Covalent

∆∆EN ValuesEN Values

Page 9: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

0.3 1.7

Nonpolar Covalent

Polar Covalent Ionic

EN ∆

Page 10: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Practice Problems

NaCl

Sodium’s EN = 0.9

Chlorine’s EN = 3.0

3.0 - 0.9 = 2.1

therefore it is mostly ionic

H2O

Hydrogen’s EN = 2.1

0xygen’s EN = 3.5

3.5 - 2.1 = 1.4

therefore it is polar covalent

Determine the bond type using EN values:

Page 11: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

6.2 Covalent Bonds

Chapter 6 Chapter 6 Chemical Chemical BondingBonding

Page 12: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Covalent Bonds

Page 13: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Covalent Terms• Molecule: A neutral group of atoms that are held

together by covalent bonds• Diatomic Molecule: A molecule containing only two

atoms

• Molecular Compound: A chemical compound whose simplest units are molecules

• Chemical Formula: Indicates the relative numbers of atoms of each kind of a chemical compound by using atomic symbols and numerical subscripts

• Molecular Formula: Shows the types and numbers of atoms combined in a single molecule of a molecular compound

Example: BrINClHOF

Page 14: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Bonding Forces

Electron – Electron Electron – Electron repulsive forcesrepulsive forces

Proton – Proton repulsive forces

Electron – Proton attractive forces

Page 15: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Pure Covalent Bonding

Page 16: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Bond Length Diagram

Page 17: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Bond Energy

It is the energy required to break a bond.

It gives us information about the strength of a bonding interaction.

Page 18: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Electron Dot Electron Dot NotationNotation

Page 19: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

The The OctetOctet Rule RuleChemical compounds tend to form so that each atom, by gaining, losing, or sharing electrons, has an octet of electrons in its highest occupied energy level.

Diatomic Fluorine

Page 20: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Hydrogen Chloride by the Octet Hydrogen Chloride by the Octet RuleRule

Page 21: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Formation of Water by the Octet Formation of Water by the Octet RuleRule

Page 22: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Comments About the Octet RuleComments About the Octet Rule

2nd row elements C, N, O, F observe the octet rule.

2nd row elements B and Be often have fewer than 8 electrons around themselves - they are very reactive.

3rd row and heavier elements CAN exceed the octet rule using empty valence d orbitals.

When writing Lewis structures, satisfy octets first, then place electrons around elements having available d orbitals.

Page 23: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Shows how valence electrons are arranged Shows how valence electrons are arranged among atoms in a molecule.among atoms in a molecule.

Reflects central idea that stability of a compound Reflects central idea that stability of a compound relates to noble gas electron configuration.relates to noble gas electron configuration.

Lewis Lewis StructuresStructures

Page 24: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

CH

H

H

Cl..

.. .. ..

Completing a Lewis Structure CH3Cl

Add up available valence electrons:

C = 4, H = (3)(1), Cl = 7 Total = 14

Join peripheral atoms to the central atom with electron pairs.

Complete octets on atoms other than hydrogen with remaining electrons

Make carbon the central atom

..

..

..

Page 25: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

How to Make a Lewis Dot Structure for a Molecule

• Draw the Lewis Dot Diagram for each element• Place the atom with the lowest EN value in the

center• Attach the rest of the atoms to the central• If lone electrons exist on adjacent atoms, pair

them for multiple bonds.

Page 26: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Multiple Covalent Bonds:Multiple Covalent Bonds:Double BondsDouble Bonds

•Two pairs of shared electrons

•Higher bond energy and shorter bond length than single bonds

Page 27: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Multiple Covalent Bonds:Multiple Covalent Bonds:Triple bondsTriple bonds

•Three pairs of shared electrons•Higher bond energy and shorter bond length than single or double bonds

Page 28: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

ResonanceResonanceOccurs when more than one valid Lewis structure can be written for a particular molecule.

These are resonance structures. The actual structure is an average of the resonance structures.

Page 29: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Resonance in OzoneResonance in Ozone

Neither structure is correct.

Page 30: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Resonance in a carbonate ion:

Resonance in an acetate ion:

Resonance in Polyatomic Ions

Page 31: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Covalent Network CompoundsCovalent Network CompoundsSome covalently bonded substances DO NOT form

discrete molecules.

Diamond, a network of covalently bonded carbon atoms

Graphite, a network of covalently bonded carbon atoms

Page 32: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

ModelsModels Models are attempts to explain how nature operates Models are attempts to explain how nature operates

on the microscopic level based on experiences in on the microscopic level based on experiences in the macroscopic world.the macroscopic world.

Models can be physical as with this DNA model

Models can be mathematical

Models can be theoretical or philosophical

Page 33: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Fundamental Properties of ModelsFundamental Properties of Models

A model does not equal reality.

Models are oversimplifications, and are therefore often wrong.

Models become more complicated as they age.

We must understand the underlying assumptions in a model so that we don’t misuse them.

Page 34: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

6.3 Ionic Bonding

Chapter 6 Chapter 6 Chemical Chemical BondingBonding

Page 35: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Ionic Bonds

Page 36: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Ionic BondsIonic Bonds Electrons are transferred

Electronegativity differences are generally greater than 1.7 The formation of ionic bonds is always exothermic!

Page 37: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Ionic Bonding

• Formula Unit: The simplest collection of atoms from which an ionic compound's formula can be established

• Lattice Energy: The energy released when one mole of an ionic crystalline compound is formed from gaseous ions

Na+ (g) + Cl- (g) → NaCl (s) + 787.5 kJ

• Formation of ionic compounds is ALWAYS exothermic

Page 38: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Sodium Chloride Crystal LatticeSodium Chloride Crystal LatticeIonic compounds form solids Ionic compounds form solids at ordinary temperatures.at ordinary temperatures.

Ionic compounds organize in Ionic compounds organize in a characteristic crystal lattice a characteristic crystal lattice of alternating positive and of alternating positive and negative ions.negative ions.

Formation of sodium chlorideNa = 3s1 Cl = 3s23p5

Na+ = 2s22p6 Cl- = 3s23p6

Page 39: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Polyatomic Ions

• A charged group of covalently bonded atoms• Creation of octets results in an excess or deficit

of electrons

Page 40: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

A Comparison of Ionic and Molecular Compounds

Page 41: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

6.4 Metallic Bonding

Chapter 6 Chapter 6 Chemical Chemical BondingBonding

Page 42: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

The Metallic Bond Model

• The chemical bonding that results from the attraction between metal atoms and the surrounding sea of electrons

• Electron Delocalization in Metals• Vacant p and d orbitals in metal's outer energy

levels overlap, and allow outer electrons to move freely throughout the metal

• The valence electrons do not belong to any one atom!

Page 43: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Swim in the Sea of Valence Electrons…

• In metals, the valence electrons are held loosely. The vacant p & d orbitals overlap.

• Metal atoms DO NOT lose their valence electrons in metallic bonding, rather they release them into a “Sea of Electrons”

• Although the atoms are bonded together, they are not bonded to any one particular atom, it is more like a large network.

Page 44: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Sea of Valence Electrons…

Page 45: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Bonding Between Metals• Results in an interaction that hold metal atoms

together, however, it is not called a compound.

• Special Properties result from this interaction:– Malleable- pounded/ rolled into sheets (aluminum

foil)– Ductile- Drawn into wire. (copper wires)– Conductivity- the flow of electrons– Luster- Shiny-The narrow range of energy

differences between orbitals allows electrons to be easily excited, and emit light upon returning to a lower energy level

Page 46: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Metallic Properties

• Metals are good conductors of heat and light• Metals have luster (shiny)• The narrow range of energy differences between

orbitals allows electrons to be easily excited, and emit light upon returning to a lower energy level

• Metals are Malleable- can be hammered into thin sheets

• Metals are ductile- ability to be drawn into wire• Metallic bonding is the same in all directions, so

metals tend not to be brittle

Page 47: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Metallic Bond Strength• Heat of Vaporization• The ease with which atoms in a metallic solid can be

separated from one another into individual gaseous atoms is related to bond strength

Page 48: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

6.5 Molecular Geometry

Chapter 6 Chapter 6 Chemical Chemical BondingBonding

Page 49: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

VSEPR Model

The structure around a given atom is determined principally by minimizing electron pair repulsions.

The model for predicting molecular shapes

VSEPR Theory: Repulsion between the sets of valence-level electrons surrounding an atom causes these sets to be oriented as far apart as possible

(Valence Shell Electron Pair Repulsion)

Page 50: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

VSEPR and Unshared Electron Pairs

• Unshared pairs take up positions in the geometry of molecules just as atoms do

• Unshared pairs have a relatively greater effect on geometry than do atoms

• Lone (unshared) electron pairs require more room than bonding pairs (they have greater repulsive forces) and tend to compress the angles between bonding pairs

• Lone pairs do not cause distortion when bond angles are 120° or greater

Page 51: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Predicting a VSEPR StructurePredicting a VSEPR Structure

Draw Lewis structure of each atom.Draw Lewis structure of each atom.

Put pairs as far apart as possible.Put pairs as far apart as possible.

Determine positions of atoms from the way Determine positions of atoms from the way electron pairs are shared.electron pairs are shared.

Determine the name of molecular structure Determine the name of molecular structure from positions of the atoms.from positions of the atoms.

Page 52: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Molecular Shapes: Linear

• When only 2 atoms are connected, the only possible shape is a straight line, linear.

• Ex: Diatomics

Br Br

Page 53: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Molecular Shapes: Lone Pairs • When lone pairs of electrons are present

on the central atom, they may shift the shape of the molecule. These are pairs of electrons that are not involved in a bond.

O HH

• They occupy space and provide negative repulsion forces against other electrons. They can repel more strongly than a bonded pair.

Page 54: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Molecular Shapes: Repulsion

• Electrons want to spread out around the central atom.

• They want to be as far away from each other as possible, due to negative-negative repulsion.

• They want to maximize their distance.

e-e- e-e-

Page 55: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Molecular Shapes: Bent • In water, the shape formed

in called bent, which is a variation of a tetrahedron. A tetrahedral molecule has 1 central atom and 4 attached. The bent molecule has 1 central atom and 2 attached.

O

HH

• The other 2 places are left “vacant” for the 2 lone pairs of electrons on oxygen, which occupy space and cause repulsion on the 2 bonded hydrogen atoms & cause them to be pushed downward, or away.

Page 56: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Molecular Shapes: Linear

• Not all molecules with 3 atoms will have the bent shape.

• Carbon Dioxide has 2 double bonds; one to each oxygen. This gives CO2 a linear shape by placing the double bonds as far apart as possible.

O C O

Page 57: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Molecular Shapes: Pyramidal• When you have 1 central atom with 3 attached,

there are 2 possible arrangements.

• In ammonia, NH3, there are 3 hydrogen atoms bonded to a central nitrogen. Due to the lone pair on nitrogen, the hydrogen atoms are pressed downward to form the pyramidal shape.

N

HH

H

Page 58: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Molecular Shapes: Trigonal Planar• The other possible arrangement for 1 central atom

with 3 attached is called trigonal planar.

• In BCl3, the 3 chlorine atoms are bonded to a central boron atom. However, the boron atom does NOT have a lone pair. Therefore, there is not additional pressure placed on the 3 chlorine bonds, so they spread out equally around the central atom.

B

Cl Cl

Cl

Page 59: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Molecular Shapes: Tetrahedral

• When 4 atoms are bonded to 1 central atom, the shape is called tetrahedral.

• In methane, CH4, 4 hydrogen atoms are bonded to 1 central carbon.

CHH

H

H

Page 60: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Table of Molecular Shapes# of

AtomsStructures

Bond Angles

Shape Name

2 180° Linear

3 105° Bent

4 120°Trigonal Planar

4 107° Pyramidal

5 109.5° Tetrahedral

Page 61: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Table – VSEPR Structures

Page 62: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

VSEPR & The Water Molecule

Page 63: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

VSEPR & The Ammonia Molecule

Page 64: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

VSEPR & Xenon Tetrafluoride

Which one will it be???

Page 65: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

VSEPR & Phosphorus Hexachloride

Page 66: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

How to Determine Polarity of a Molecule

• Draw the molecule’s shape according to the Lewis Structure and VSEPR

• Fill in the EN values, and determine the difference for each bond

• Determine the bond type for each bond in the molecule

• Add in partial (δ) + and partial (δ) – symbols• Determine if there is a divisible axis to

separate the partial + from the partial -

Page 67: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Molecular Polarity • If your molecule has polar bonds, it may be a polar

molecule. • Polar molecules have specialspecial properties that result

from partial positive and negative ends of the entire molecule.

• Polar molecules can also be called dipoles. • These molecules are attracted to one another.

δ = partial

Page 68: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Molecular Polarity

• Water is a bent molecule, with 2 polar bonds.

• Since all of the negative charge is distributed on 1 side of the molecule, and all the positive charge is on the opposite side, water is a polar molecule.

O

HH

δ+

2 δ-

δ+

Page 69: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Molecular Polarity • Not all atoms with polar bonds are polar

molecules!

• Carbon Dioxide has all polar bonds. However, its geometry prohibits overall polarity since there are no distinct ends splitting the positive & negative charges.

O C O

δ- 2δ+ δ-

• CO2, therefore, is a non-polar molecule.

Page 70: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

HybridizationHybridization

The Blending of OrbitalsThe Blending of Orbitals

Page 71: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

We have studied electron configuration notation and the sharing of electrons in the formation of covalent bonds.

Methane is a simple natural gas. Its molecule has a carbon atom at the center with four hydrogen atoms covalently bonded around it.

Lets look at amolecule of methane, CH4.

Page 72: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

What is the expected orbital notation of carbonin its ground state?

(Hint: How many unpaired electrons does this carbon atom have available for bonding?)

Can you see a problem with this?

Carbon ground state configuration

Page 73: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

You should conclude that You should conclude that carbon only has carbon only has TWOTWO electrons available for electrons available for bonding. bonding. That is not enough for a full That is not enough for a full octet!octet!

How does carbon overcome this problem so thatHow does carbon overcome this problem so thatit may form four bonds?it may form four bonds?

Carbon’s Bonding ProblemCarbon’s Bonding Problem

Page 74: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

The first thought that The first thought that chemists had was that chemists had was that carbon promotes one of its carbon promotes one of its 2s2s electrons… electrons…

…to the empty 2p orbital.

Carbon’s Empty OrbitalCarbon’s Empty Orbital

Page 75: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

However, they quickly recognized a problem with such an arrangement…

Three of the carbon-hydrogen bonds would involve an electron pair in which the carbon electron was a 2p, matched with the lone 1s electron from a hydrogen atom.

Page 76: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

This would mean that three of the bonds in a methane molecule would be identical, because they would involve electron pairs of equal energy.

But what about the fourth bond…?

Unequal bond energy

Page 77: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

The fourth bond is between a 2s electron from thecarbon and the lone 1s hydrogen electron.

Such a bond would have slightly less energy than the other bonds in a methane molecule.

Unequal bond energy #2

Page 78: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

This bond would be slightly different in character than the other three bonds in methane.

This difference would be measurable to a chemistby determining the bond length and bond energy.

But is this what they observe?

Unequal bond energy #3

Page 79: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

The simple answer is, “No”.

Chemists have proposed an explanation calledHybridization.

Hybridization is the combining of two or more orbitals of nearly equal energy within the same atom into orbitals of equal energy.

Measurements show that all four bonds in methane are equal. Thus, we need a new explanation for the bonding in methane.

Page 80: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

In the case of methane, they call the hybridization sp3, meaning that an s orbital is combined with threep orbitals to create four equal hybrid orbitals.

These new orbitals have slightly MORE energy thanthe 2s orbital…… and slightly LESS energy than the 2p orbitals.

sp3 Hybrid Orbitals

Page 81: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Here is another way to look at the sp3 hybridizationand energy profile…

sp3 Hybrid Orbitals

Page 82: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

While sp3 is the hybridization observed in methane,there are other types of hybridization that atoms undergo.

These include sp hybridization, in which one s orbital combines with a single p orbital.

Notice that this produces two hybrid orbitals, whileleaving two normal p orbitals

sp Hybrid Orbitals

Page 83: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Another hybrid is the sp2, which combines two orbitals from a p sublevel with one orbital from an s sublevel.

Notice that one p orbital remains unchanged.

sp2 Hybrid Orbitals

Page 84: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Predicting the Geometry of Hybridized Orbitals

Page 85: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Intermolecular Forces

• Forces of attraction between molecules• Generally weaker than bonds that join atoms in

molecules• Boiling point gives a rough estimate of

intermolecular forces• high bp = large attractive forces• low bp = small attractive forces

Page 86: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Molecular Polarity and Dipole-Dipole Forces

• Dipole- Created by equal but opposite charges that are separated by a short distance

• A dipole is represented by an arrow with a head pointing toward the negative pole and a crossed tail situated at the positive pole

Page 87: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

PolarityPolarity A molecule, such as HF, that has a center of A molecule, such as HF, that has a center of

positive charge and a center of negative positive charge and a center of negative charge is said to be polar, or to have a dipole charge is said to be polar, or to have a dipole moment.moment.

+

FH

This symbol means “partial”

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Polar Covalent Bonding

• δ = partial

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Dipole-Dipole forces

• The negative region of one molecule is attracted to the positive region of another molecule

• A polar molecule can induce a dipole in a nonpolar molecule by temporarily attracting its electrons

Page 90: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Dipole-Dipole Dipole-Dipole AttractionsAttractions

Attraction between oppositely charged regions of neighboring molecules.

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The Water Dipole

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The Ammonia Dipole

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Polarity• Water is a polar molecule. • (A molecule with partially

positive & negative ends due to differences in electronegativity)

• Its electrons are shared unequally so it is a dipole.

• Causes strong intermolecular attractions.

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Hydrogen Bonding

• The intermolecular force in which a hydrogen atom that is bonded to a highly electronegative atom (F, O, N) is attracted to an unshared pair of electrons of an electronegative atom in a nearby molecule

• It is usually represented by dotted lines

Page 95: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

Hydrogen Bonds

• When the partial positive, or hydrogen end of a molecule is attracted to the partial negative, or oxygen end of another molecule we call it a Hydrogen bond.

• It is an attraction! • Hydrogen, and Fluorine, Oxygen

& Nitrogen. (F-O-N)

(high electronegativity values)

Page 96: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

H-Bonds

• Diagram of H-bonds

• Solid lines are normal bonds

• Dotted lines are H-bonds

Page 97: Chapter 6 -Chemical Bonding A steroid alkaloid derived from skin secretions of the Phyllobates and Dendrobates genera of South American poison- arrow

H-Bonds• Molecules containing

hydrogen bonds, like water, have very high points.

• Why might this occur?• Hydrogen bonds are

strong -holds molecules together.

• It takes a lot of energy to break apart these attractions to liberate each molecule into the gaseous state.

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Hydrogen BondingHydrogen Bonding

Hydrogen bonding is used in Kevlar, a strong polymer used in bullet-proof vests.

Bonding between hydrogen and more electronegative neighboring atoms such as oxygen and nitrogen

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Hydrogen Hydrogen Bonding Bonding in Waterin Water

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Hydrogen Bonding Between Ammonia & Water

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London Dispersion ForcesLondon Dispersion Forcesaka Van Der Waals Forcesaka Van Der Waals Forces

The temporary separations of charge The temporary separations of charge that lead to the London force that lead to the London force attractions are what attract one attractions are what attract one nonpolar molecule to its neighbors.nonpolar molecule to its neighbors.

Fritz LondonFritz London1900-19541900-1954

•All molecules experience London All molecules experience London forces forces •London forces increase with the size London forces increase with the size of the molecules.of the molecules.

• London forces are the only forces of attraction London forces are the only forces of attraction among noble-gas atoms, nonpolar, and slightly among noble-gas atoms, nonpolar, and slightly polar moleculespolar molecules

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London Forces in HydrocarbonsLondon Forces in Hydrocarbons

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Comparison of Boiling Points & Bond Types

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Relative Magnitudes of ForcesRelative Magnitudes of ForcesThe types of bonding forces vary in their The types of bonding forces vary in their strength as measured by average bond strength as measured by average bond energy.energy.

Covalent bonds (400 kcal)

Hydrogen bonding (12-16 kcal )

Dipole-dipole interactions (2-0.5 kcal)

London forces (less than 1 kcal)

Strongest

Weakest