1 Chapter 6, Section 6.1 Introduction to Chemical Bonding i) Define chemical bond. Objectives ii) Explain why most atoms form chemical bonds. iii) Describe ionic and covalent bonding. iv) Explain why most chemical bonding is neither purely ionic nor purely covalent. v) Classify bonding type according to electronegativity differences.
2 Chemical Bond
3 Ionic Bond
4 Covalent Bond
5 Comparing Polar and Nonpolar Covalent Bonds
6 Using Electronegativity Difference to Classify Bonding
7 Sample Problems Using Electronegativity Magnitudes to Classify Bonds Classify the bonds between sulfur, S, and the following elements: i) hydrogen, H; ii) cesium, Cs; and iii) chlorine, Cl. In each pair, which atom will be more negative?
8 Classify the bond between sulfur, S, and hydrogen, H Electronegativity of Sulfur (S) = 2.5 Electronegativity of hydrogen (H ) = 2.1 Difference = = 0.4 = Polar-covalent More negative atom = Sulfur (S) since 2.5 > 2.1
9 Classify the bond between sulfur, S, and cesium, Cs Electronegativity of Sulfur (S) = 2.5 Electronegativity of cesium (Cs)= 0.7 Difference = = 1.8 = Ionic More negative atom = Sulfur (S) since 2.5 > 0.7
10 Classify the bond between sulfur, S, and cesium, Cs Electronegativity of Sulfur (S) = 2.5 Electronegativity of chlorine (Cl) = 3.0 Difference = = 0.5 = Polar-covalent More negative atom = chlorine (Cl) = 3.0 > 2.5
11 Chapter 6, Section 6.2 Covalent Bonding and Molecular Compounds Objectives i) Define molecule and molecular formula. ii) Explain the relationships among potential energy, distance between approaching atoms, bond length, and bond energy. iii) State the octet rule. iv) List the six basic steps used in writing Lewis structures. v) Explain how to determine Lewis structures for molecules containing single bonds, multiple bonds, or both. vi) Explain why scientists use resonance structures to represent some molecules.
12 Molecular Compounds A molecule is a neutral group of atoms that are held together by covalent bonds. A chemical compound whose simplest units are molecules is called a molecular compound.
14 Molecular Compounds The composition of a compound is given by its chemical formula. A chemical formula indicates the relative numbers of atoms of each kind in a chemical compound by using atomic symbols and numerical subscripts. A molecular formula shows the types and numbers of atoms combined in a single molecule of a molecular compound.
15 Chemical Formula
16 Molecular Compounds Structure of the water molecule
17 Molecular Compounds Comparing Monatomic, Diatomic, and Polyatomic Molecules
18 Formation of a Covalent Bond Most atoms have lower potential energy when they are bonded to other atoms than they have as they are independent particles. In example potential energy changes during the formation of a hydrogen-hydrogen bond.
19 Formation of a Covalent Bond The electron of one atom and proton of the other atom attract one another. The two nuclei and two electrons repel each other. These two forces cancel out to form a covalent bond at a length where the potential energy is at a minimum.
20 Formation of a Covalent Bond
21 Characteristics of a Covalent Bond The distance between two bonded atoms at their minimum potential energy (the average distance between two bonded atoms) is the bond length. In forming a covalent bond, the hydrogen atoms release energy. The same amount of energy must be added to separate the bonded atoms. Bond energy is the energy required to break a chemical bond and form neutral isolated atoms.
22 Covalent Bond Length
23 Bond Energy
24 Covalent Bond Length and Energies for Single Bonds
25 Characteristics of a Covalent Bond When two atoms form a covalent bond, their shared electrons form overlapping orbitals. This achieves a noble-gas configuration. The bonding of two hydrogen atoms allows each atom to have the stable electron configuration of helium, 1s2.
26 Premise to The Octet Rule Noble gas atoms are unreactive because their electron configurations are especially stable. This stability results from the fact that the noble-gas atoms outer s and p orbitals are completely filled by a total of eight electrons. Other atoms can fill their outermost s and p orbitals by sharing electrons through covalent bonding.
27 The Octet Rule Such bond formation follows the octet rule: Compounds tend to form so that each atom, by gaining, losing, or sharing electrons, has an octet (Eight) of electrons in its highest energy level.
28 The Octet Rule
29 Exceptions to the Octet Rule Exceptions to the octet rule include those for atoms that cannot fit eight electrons, and for those that can fit more than eight electrons, into their outermost orbital. 1) Hydrogen forms bonds in which it is surrounded by only two electrons. 2) Boron has just three valence electrons, so it tends to form bonds in which it is surrounded by six electrons. 3) Main-group elements in Periods 3 and up can form bonds with expanded valence, involving more than eight electrons.
30 Electron-Dot Notation To keep track of valence electrons, it is helpful to use electron-dot notation. Electron-dot notation is an electron-configuration notation in which only the valence electrons of an atom of a particular element are shown, indicated by dots placed around the element s symbol. The inner-shell electrons are not shown.
31 Electron Dot Notation
32 Electron-Dot Notation Example: A hydrogen atom has only one occupied energy level, the n = 1 level, which contains a single electron. The group notation for nitrogen s family of elements is ns 2 np 3. Nitrogen has five valence electrons.
33 Lewis Structures Electron-dot notation can also be used to represent molecules. The pair of dots between the two symbols represents the shared electron pair of the hydrogen-hydrogen covalent bond.
34 Lewis Structures For a molecule of fluorine, F 2, the electron-dot notations of two fluorine atoms are combined. The pair of dots between the two symbols represents the shared pair of a covalent bond. Unshared pair(s), also called a lone pair, is a pair of electrons that is not involved in bonding and that belongs exclusively to one atom.
35 Lewis Structures
36 Lone Pairs of Electrons
37 Lewis Structures The pair of dots representing a shared pair of electrons in a covalent bond is often replaced by a long dash.
38 Lewis Structures A structural formula indicates the kind, number, and arrangement, and bonds but not the unshared pairs of the atoms in a molecule.
39 Structural Formula
40 Lewis Structures The Lewis structures and the structural formulas for many molecules can be drawn if one knows the composition of the molecule and which atoms are bonded to each other. A single covalent bond, or single bond, is a covalent bond in which one pair of electrons is shared between two atoms.
41 ******Rules of Drawing Lewis Structures****** 1) Determine the type and number of atoms in the molecule. 2) Write the electron-dot notation for each type of atom in the molecule. 3) Determine the total number of valence electrons available in the atoms to be combined. 4) If carbon is present, it is the central atom. Otherwise, the leastelectronegative atom is central. Hydrogen, is never central. 5) Add unshared pairs of electrons to each nonmetal atom (except hydrogen) such that each is surrounded by eight electrons.
42 Lewis Structures (EXAMPLE) Draw the Lewis structure of iodomethane, CH 3 I 1) Determine the type and number of atoms in the molecule. The formula shows one carbon atom, one iodine atom, and three hydrogen atoms.
43 Lewis Structures (EXAMPLE - Continued) Draw the Lewis structure of iodomethane, CH 3 I 2) Write the electron-dot notation for each type of atom in the molecule. Carbon is from Group 14 and has four valence electrons. Iodine is from Group 17 and has seven valence electrons. Hydrogen has one valence electron.
44 Lewis Structures (EXAMPLE - Continued) Draw the Lewis structure of iodomethane, CH 3 I 3) Determine the total number of valence electrons available in the atoms to be combined. Atom Valence Electrons Per Atom # of Atoms Total Electrons ( e - ) C 4 1 = 4 x 1 = 4 H 1 3 = 1 x 3 = 3 I 7 1 = 7 x 1 = 7 = sum = 14 e -
45 Lewis Structures (EXAMPLE - Continued) Draw the Lewis structure of iodomethane, CH 3 I 4) If carbon is present, it is the central atom. Otherwise, the leastelectronegative atom is central. Hydrogen, is never central. 5) Add unshared pairs of electrons to each nonmetal atom (except hydrogen) such that each is surrounded by eight electrons.
46 Multiple Covalent Bonds A double covalent bond, or simply a double bond, is a covalent bond in which two pairs of electrons are shared between two atoms. Double bonds are often found in molecules containing carbon, nitrogen, and oxygen.
47 Multiple Covalent Bonds A triple covalent bond, or simply a triple bond, is a covalent bond in which three pairs of electrons are shared between two atoms. i.e. Diatomic Nitrogen and Ethyne (Acetylene). Species Involved : Nitrogen, Carbon and Hydrogen
48 Multiple Covalent Bonds A triple covalent bond, or simply a triple bond, is a covalent bond in which three pairs of electrons are shared between two atoms. i.e. Diatomic Nitrogen and Ethyne (Acetylene) or or
49 Multiple Covalent Bonds A double bond is shown either by two side-by-side pairs of dots or by two parallel dashes. or
50 Comparing Single, Double, and Triple Bonds
51 Multiple Covalent Bonds Double and triple bonds are referred to as multiple bonds, or multiple covalent bonds. In general, double bonds have greater bond energies and are shorter than single bonds. Triple bonds are even stronger and shorter than double bonds. When writing Lewis structures for molecules that contain carbon, nitrogen, or oxygen, remember that multiple bonds between pairs of these atoms are possible.
52 Drawing Lewis Structures with Many Atoms
53 Drawing Lewis Structures with Many Atoms
54 Multiple Covalent Bonds Example - Draw the Lewis structure for methanal, CH 2 O, which is also known as formaldehyde. 1) Determine the number of atoms of each element present in the molecule. The formula shows one carbon atom, two hydrogen atoms, and one oxygen atom.
55 Multiple Covalent Bonds Example - Draw the Lewis structure for methanal, CH 2 O, which is also known as formaldehyde. 2) Write the electron-dot notation for each type of atom. Carbon is from Group 14 and has four valence electrons. Oxygen, which is in Group 16, has six valence electrons. Hydrogen has only one valence electron.
56 Multiple Covalent Bonds Example - Draw the Lewis structure for methanal, CH 2 O, which is also known as formaldehyde. 3) Determine the total number of valence electrons available in the atoms to be combined. Atom Valence Electrons Per Atom # of Atoms Total Electrons ( e - ) C 4 1 = 4 x 1 = 4 H 1 2 = 1 x 2 = 2 O 6 1 = 6 x 1 = 6 = sum = 12 e -
57 Multiple Covalent Bonds Example - Draw the Lewis structure for methanal, CH 2 O, which is also known as formaldehyde. 4) Arrange the atoms to form a skeleton structure for the molecule. Connect the atoms by electron-pair bonds.
58 Multiple Covalent Bonds Example - Draw the Lewis structure for methanal, CH 2 O, which is also known as formaldehyde. 5) Add unshared pairs of electrons to each nonmetal atom (except hydrogen) such that each is surrounded by eight electrons.
59 Multiple Covalent Bonds Example - Draw the Lewis structure for methanal, CH 2 O, which is also known as formaldehyde. 6a) Count the electrons in the Lewis structure to be sure that the number of valence electrons used equals the number available. The structure has 14 electrons. The structure has two valence electrons too many.
60 Multiple Covalent Bonds Example - Draw the Lewis structure for methanal, CH 2 O, which is also known as formaldehyde. 6b) Subtract one or more lone pairs until the total number of valence electrons is correct. Atom Valence Electrons Per Atom # of Atoms Total Electrons ( e - ) C 4 1 = 4 x 1 = 4 H 1 2 = 1 x 2 = 2 O 6 1 = 6 x 1 = 6 = sum = 12 e -
61 Multiple Covalent Bonds Example - Draw the Lewis structure for methanal, CH 2 O, which is also known as formaldehyde. 6b) Continued Move one or more lone electron pairs to existing bonds until the outer shells of all atoms are completely filled. Subtract the lone pair of electrons from the carbon atom. Move one lone pair of electrons from the oxygen to the bond between carbon and oxygen to form a double bond. or
62 Atomic Resonance
63 Chapter 6, Section 6.3 Ionic Bonding and Ionic Compounds Objectives i) Compare a chemical formula for a molecular compounds with one for an ionic compound. ii) Discuss the arrangements of ions in crystals. iii) Define lattice energy and explain its significance. iv) List and compare the distinctive properties of ionic and molecular compounds. v) Write the Lewis structure for a polyatomic ion given the identity of the atoms combined and other appropriate information.
64 Ionic Compounds Most of the rocks and minerals that make up Earth s crust consist of positive and negative ions held together by ionic bonding. Example: Table salt, NaCl, consists of sodium and chloride ions combined in a one-to-one ratio (Na + Cl - ) so that each positive charge is balanced by a negative charge.
65 Ionic Compounds An ionic compound is composed of positive and negative ions that are combined so that the numbers of positive and negative charges are equal. Most ionic compounds exist as crystalline solids. A crystal of any ionic compound is a three-dimensional network of positive and negative ions mutually attracted to each other.
66 Ionic Compounds In contrast to a molecular compound, an ionic compound is not composed of independent, neutral units that can be isolated. The chemical formula of an ionic compound represents not molecules, but the simplest ratio of the compound s ions. A formula unit is the simplest collection of atoms from which an ionic compound s formula can be established.
67 Ionic Vs. Covalent Bonding
68 Formation of Ionic Compounds The sodium atom has two valence electrons and the chlorine atom has seven valence electrons.
69 Formation of Ionic Compounds Sodium + Chlorine -> Sodium + Chlorine Atom Atom Cation Anion Atoms of sodium and other alkali metals easily lose one electron to form cations. Atoms of chlorine and other halogens easily gain one electron to form anions.
70 Formation of Ionic Compounds In an ionic crystal, ions minimize their potential energy by combining in an orderly arrangement known as a crystal lattice. Attractive forces exist between oppositely charged ions within the lattice. Repulsive forces exist between like-charged ions within the lattice.
71 Formation of Ionic Compounds The combined attractive and repulsive forces within a crystal lattice determine: i) The distances between ions ii) The pattern of the ions arrangement in the crystal
72 Characteristics of Ion Bonding in a Crystal Lattice
73 NaCl and CsCl Crystal Lattices
74 Lattice Energy
75 A Comparison of Ionic and Molecular Compounds The force that holds ions together in an ionic compound is a very strong electrostatic attraction. In contrast, the forces of attraction between molecules of covalent compounds are much weaker. This difference in the strength of attraction between the basic units of molecular and ionic compounds gives rise to different properties between the two types of compounds.
76 Comparison of Melting and Boiling Points of Covalent and Ionic Bonded Compounds
77 How to Identify a Compound as Ionic
78 How to Identify a Compound as Ionic
79 Comparing Ionic and Molecular Compounds
80 Polyatomic Ions Certain atoms bond covalently with each other to form a group of atoms that has both molecular and ionic characteristics. A charged group of covalently bonded atoms is known as a polyatomic ion. Like other ions, polyatomic ions have a charge that results from either a shortage or excess of electrons.
81 Polyatomic Ions An example of a polyatomic ion is the ammonium ion: (NH 4 ) + It is written in this manner to show that the group of atoms as a whole has a charge of 1+. The charge of the ammonium ion is determined as follows: The seven protons in the nitrogen atom plus the four protons in the four hydrogen atoms give the ammonium ion a potential total positive charge of (11+). One of their electrons is lost, giving the polyatomic ion a total negative charge of (-10).
82 Polyatomic Ions Some examples of Lewis structures of polyatomic ions are shown below.
83 Comparing Monatomic, Polyatomic, and Diatomic Structures
84 Chapter 6, Section 6.4 Metallic Bonding Objectives i) Describe the electron-sea model of metallic bonding, and explain why metals are good electrical conductors. ii) Explain why metal surfaces are shiny. iii) Explain why metals are malleable and ductile but ionic-crystalline compound are not.
85 Metallic Bonding Chemical bonding is different in metals than it is in ionic, molecular, or covalent-network compounds. The unique characteristics of metallic bonding gives metals their characteristic properties, listed below. i) Electrical conductivity ii) Thermal conductivity iii) Malleability iv) Ductility v) Shiny appearance
86 Properties of Substances with Metallic, Ionic, and Covalent Bonds
87 The Metallic-Bond Model In a metal, the vacant orbitals in the atoms outer energy levels overlap. This overlapping of orbitals allows the outer electrons of the atoms to roam freely throughout the entire metal. The electrons are delocalized, which means that they do not belong to any one atom but move freely about the metal s network of empty atomic orbitals. These mobile electrons form a sea of electrons around the metal atoms, which are packed together in a crystal lattice. The chemical bonding that results from the attraction between metal atoms and the surrounding sea of electrons is called metallic bonding
88 Metallic Bonding
89 Properties of Metals: Surface Appearance
90 Properties of Metals: Malleability and Ductility
91 Properties of Metals: Electrical and Thermal Conductivity
92 i) Explain VSEPR theory. Chapter 6, Section 6.5 Molecular Geometry Objectives ii) Predict the shapes of molecules or polyatomic ions using VSEPR theory. iii) Explain how the shapes of molecules are accounted for by hybridization theory. iv) Describe dipole-dipole forces, hydrogen bonding, induced dipoles, and London dispersion forces and their effects on properties such as boiling and melting points. v) Explain the shapes of molecules or polyatomic ions using VSEPR theory.
93 Molecular Geometry The properties of molecules depend not only on the bonding of atoms but also on molecular geometry: the three-dimensional arrangement of a molecule s atoms. The polarity of each bond, along with the geometry of the molecule, determines molecular polarity, or the uneven distribution of molecular shape. Molecular polarity strongly influences the forces that act between molecules in liquids and solids. A chemical formula, by itself, reveals little information about a molecule s geometry.
94 VSEPR Theory As shown at right, diatomic molecules, like those of a) hydrogen (H 2 ) and b) hydrogen chloride (HCl) can only be linear because they consist of only two atoms. To predict the geometries of more-complicated molecules, one must consider the locations of all electron pairs surrounding the bonding atoms. This is the basis of VSEPR theory
95 VSEPR Theory The abbreviation VSEPR (say it VES-pur ) stands for valence-shell electron-pair repulsion. VSEPR theory states that repulsion between the sets of valence-level electrons surrounding an atom causes these sets to be oriented as far apart as possible.
96 VSEPR Theory Example (Beryllium Flouride, BeF 2 ) The central beryllium atom is surrounded by only the two electron pairs it shares with the fluorine atoms. According to VSEPR, the shared pairs will be as far away from each other as possible, so the bonds to fluorine will be 180 apart from each other. The molecule will therefore be linear.
97 VSEPR Theory Representing the central atom in a molecule by A and the atoms bonded to the central atom by B, then according to VSEPR theory, BeF 2 is an example of an AB 2 molecule, which is linear. In an AB 3 molecule, the three A B bonds stay farthest apart by pointing to the corners of an equilateral triangle, giving 120 angles between the bonds. In an AB 4 molecule, the distance between electron pairs is maximized if each A B bond points to one of four corners of a tetrahedron.
98 VSEPR and Basic Molecular Shapes
99 VSEPR Theory Example - Use VSEPR theory to predict the molecular geometry of boron trichloride, BCl 3 In an AB 3 molecule, the three A B bonds stay farthest apart by pointing to the corners of an equilateral triangle, giving 120 angles between the bonds. First write the Lewis structure for BCl 3. Boron is in Group 13 and has three valence electrons. Chlorine is in Group 17, so each chlorine atom has seven valence electrons.
100 VSEPR Theory Determine the total number of valence electrons available in the atoms to be combined. Atom Valence Electrons Per Atom # of Atoms Total Electrons ( e - ) B 3 1 = 3 x 1 = 3 Cl 7 3 = 7 x 3 = 21 = sum = 24 e - The Lewis structure uses all 24 electrons.
101 VSEPR Theory In an AB 3 molecule, the three A B bonds stay farthest apart by pointing to the corners of an equilateral triangle, giving 120 angles between the bonds. Boron trichloride is an AB 3 type of molecule. Its geometry should therefore be trigonal-planar.
102 VSEPR Theory VSEPR theory can also account for the geometries of molecules with unshared electron pairs. Examples are ammonia (NH 3 ) and water (H 2 O) The Lewis Structure of ammonia shows that the central nitrogen atom has an unshared electron pair: VSEPR theory postulates that the lone pair occupies space around the nitrogen atom just as the bonding pairs do.
103 VSEPR Theory Taking into account its unshared electron pair, NH 3 takes a tetrahedral shape, as in an AB 4 molecule. The shape of a molecule refers to the positions of atoms only. The geometry of an ammonia molecule is that of a pyramid with a triangular base. In an AB 4 molecule, the distance between electron pairs is maximized if each A B bond points to one of four corners of a tetrahedron.
104 VSEPR Theory H 2 O has two unshared pairs, and its molecular geometry takes the shape of a bent, or angular, molecule. Unshared electron pairs repel other electron pairs more strongly than bonding pairs do. This is why the bond angles in ammonia and water are somewhat less than the bond angles of a perfectly tetrahedral molecule.
105 VSEPR and Lone Electron Pairs
106 VSEPR Theory The same basic principles of VSEPR theory that have been described can be used to determine the geometry of several additional types of molecules, such as AB 2 E, AB 2 E 2, AB 5, and AB 6. Treat double and triple bonds the same way as single bonds. Treat polyatomic ions similarly to molecules. The next few slides shows several more examples of molecular geometries determined by VSEPR theory.
107 VSEPR and Molecular Geometry
108 VSEPR and Molecular Geometry
109 VSEPR Theory Use VSEPR theory to predict the shape of a molecule of carbon dioxide, CO 2. Draw the Lewis structure of carbon dioxide. There are two carbon-oxygen double bonds and no unshared electron pairs on the carbon atom. This is an AB 2 molecule, which is linear.
110 VSEPR Theory Use VSEPR theory to predict the shape of a chlorate ion, (ClO 3 ) -1 Draw the Lewis structure of chlorate ion. There are three oxygen atoms bonded to the central chlorine atom, which has an unshared electron pair. This is an AB 3 E molecule, which is trigonal-pyramidal.
111 Hybridization VSEPR theory is useful for predicting and explaining the shapes of molecules. A step further must be taken to explain how the orbitals of an atom are rearranged when the atom forms covalent bonds. For this purpose, we use the Model of hybridization, which is the mixing of two or more atomic orbitals of similar energies on the same atom to produce new hybrid atomic orbitals of equal energies.
112 Hybridization Take the simple example of methane, CH4. The carbon atom has four valence electrons, two in the 2s orbital and two in 2p orbitals. Experiments have determined that a methane molecule is tetrahedral. How does carbon form four equivalent, tetrahedrally arranged, covalent bonds? 1) Recall that s and p orbitals have different shapes. To achieve four equivalent bonds, carbon s 2s and three 2p orbitals hybridize to form four new, identical orbitals called sp3 orbitals. 2) The superscript 3 on the p indicates that there are three p orbitals included in the hybridization. The superscript 1 on the s is left out, like in a chemical formula.
113 Hybridization The four (s + p + p + p) hybrid orbitals in the sp3-hybridized methane molecule are equivalent: they all have the same energy, which is greater than that of the 2s orbital but less than that of the 2p orbitals. Hybrid orbitals are orbitals of equal energy produced by the combination of two or more orbitals on the same atom. Hybridization explains the bonding and geometry of many molecules.
114 Geometry of Hybrid Orbitals
115 Hybrid Orbitals
116 Intermolecular Forces Boiling points for ionic compounds and metals tend to be much higher than those for molecular substances: forces between molecules are weaker than those between metal atoms or ions. The forces of attraction between molecules are known as intermolecular forces. The boiling point of a liquid is a good measure of the intermolecular forces between its molecules: the higher the boiling point, the stronger the forces between the molecules. Intermolecular forces vary in strength but are generally weaker than bonds between atoms within molecules, ions in ionic compounds, or metal atoms in solid metals.
117 Comparing Ionic and Molecular Substances
118 Intermolecular Forces The strongest intermolecular forces exist between polar molecules. Because of their uneven charge distribution, polar molecules have dipoles. A dipole is created by equal but opposite charges that are separated by a short distance. The direction of a dipole is from the dipole s positive pole to its negative pole. A dipole is represented by an arrow with its head pointing toward the negative pole and a crossed tail at the positive pole. The dipole created by a hydrogen chloride molecule is indicated as:
119 Intermolecular Forces The negative region in one polar molecule attracts the positive region in adjacent molecules. So the molecules all attract each other from opposite sides. Such forces of attraction between polar molecules are known as dipole-dipole forces. Dipole-dipole forces act at short range, only between nearby molecules. Dipole-dipole forces explain, for example the difference between the boiling points of iodine chloride, I Cl (97 C), and bromine, Br Br (59 C).
120 Comparing Dipole-Dipole Forces
121 Dipole-Dipole Forces
122 Intermolecular Forces A polar molecule can induce a dipole in a nonpolar molecule by temporarily attracting its electrons. The result is a short-range intermolecular force that is somewhat weaker than the dipole-dipole force. Induced dipoles account for the fact that a nonpolar molecule, oxygen, O 2, is able to dissolve in water, a polar molecule.
123 Dipole-Induced Dipole Interaction
124 Intermolecular Forces Some hydrogen-containing compounds have unusually high boiling points. This is explained by a particularly strong type of dipole-dipole force. In compounds containing H F, H O, or H N bonds, the large electronegativity differences between hydrogen atoms and the atoms they are bonded to make their bonds highly polar. This gives the hydrogen atom a positive charge that is almost half as large as that of a bare proton.
125 Intermolecular Forces Hydrogen bonds are usually represented by dotted lines connecting the hydrogen-bonded hydrogen to the unshared electron pair of the electronegative atom to which it is attracted. An excellent example of hydrogen bonding is that which occurs between water molecules. The strong hydrogen bonding between water molecules accounts for many of water s characteristic properties. The small size of the hydrogen atom allows the atom to come very close to an unshared pair of electrons in an adjacent molecule. The intermolecular force in which a hydrogen atom that is bonded to a highly electronegative atom is attracted to an unshared pair of electrons of an electronegative atom in a nearby molecule is known as hydrogen bonding.
126 Hydrogen Bonding
127 London Dispersion Forces Even noble gas atoms and nonpolar molecules can experience weak intermolecular attraction. In any atom or molecule polar or nonpolar the electrons are in continuous motion. As a result, at any instant the electron distribution may be uneven. A momentary uneven charge can create a positive pole at one end of an atom of molecule and a negative pole at the other.
128 London Dispersion Forces This temporary dipole can then induce a dipole in an adjacent atom or molecule. The two are held together for an instant by the weak attraction between temporary dipoles. The intermolecular attractions resulting from the constant motion of electrons and the creation of instantaneous dipoles are called London dispersion forces. Fritz London first proposed their existence in 1930.
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Part B 2 Allow a total of 15 credits for this part. The student must answer all questions in this part. 51  Allow 1 credit for 3 Mg(s) N 2 (g) Mg 3 N 2 (s). Allow credit even if the coefficient 1 is
Forensic Science Standards and Standard 1: Understands and applies principles of scientific inquiry Power : Identifies questions and concepts that guide science investigations Uses technology and mathematics
Name: Class: Date: Unit 11 Practice Multiple Choice Identify the choice that best completes the statement or answers the question. 1) Crystalline solids. A) have their particles arranged randomly B) have
Organic Functional Groups Chapter 7 Alcohols, Ethers and More 1 What do you do when you are in Pain? What do you do when you are in a lot of pain? 2 Functional Groups A functional group is an atom, groups
Chapter 1: Moles and equations 1 Learning outcomes you should be able to: define and use the terms: relative atomic mass, isotopic mass and formula mass based on the 12 C scale perform calculations, including
Electron Counting in Organometallic Chemistry 1. The 18-Electron Rule; definition & rationalisation The constitution and structure of main group element complexes can be predicted and rationalised by a
TÜRK FEN EĞİTİMİ DERGİSİ Yıl 7, Sayı 2, Haziran 2010 N Journal of TURKISH SCIENCE EDUCATION Volume 7, Issue 2, June 2010 http://www.tused.org Secondary School Students Misconceptions of Covalent Bonding
EXAMPLE EXERCISE 4.1 Change of Physical State State the term that applies to each of the following changes of physical state: (a) Snow changes from a solid to a liquid. (b) Gasoline changes from a liquid
10 CHEMICAL QUANTITIES SECTION 10.1 THE MOLE: A MEASUREMENT OF MATTER (pages 287 296) This section defines the mole and explains how the mole is used to measure matter. It also teaches you how to calculate
The Nature of Molecules Chapter 2 Energy and Metabolism Chapter 6 Chemical Bonds Molecules are groups of atoms held together in a stable association. Compounds are molecules containing more than one type
Name: Class: Date: ID: A Unit 12 Practice Test Multiple Choice Identify the choice that best completes the statement or answers the question. 1) A solid has a very high melting point, great hardness, and
Woods Chem-1 Lec-02 10-1 Atoms, Ions, Mole (std) Page 1 ATOMIC THEORY, MOLECULES, & IONS Proton: A positively charged particle in the nucleus Atomic Number: We differentiate all elements by their number
INTDUCTIN T LEWIS ACID-BASE CEMISTY DEINITINS Lewis acids and bases are defined in terms of electron pair transfers. A Lewis base is an electron pair donor, and a Lewis acid is an electron pair acceptor.
A Review of General hemistry ELETRS, BDS, AD MLEULAR PRPERTIES DID YU EVER WDER... what causes lightning? Believe it or not, the answer to this question is still the subject of debate (that s right scientists
ION EXCHANGE FOR DUMMIES An introduction Water Water is a liquid. Water is made of water molecules (formula H 2 O). All natural waters contain some foreign substances, usually in small amounts. The water
Atoms, Ions and Molecules The Building Blocks of Matter Chapter 2 1 Chapter Outline 2.1 The Rutherford Model of Atomic Structure 2.2 Nuclides and Their Symbols 2.3 Navigating the Periodic Table 2.4 The
Chapter 4, Lesson 4: Energy Levels, Electrons, and Covalent Bonding Key Concepts The electrons on the outermost energy level of the atom are called valence electrons. The valence electrons are involved
P. Table & E Configuration Practice TEST Multiple Choice Identify the choice that best completes the statement or answers the question. 1. A line spectrum is produced when an electron moves from one energy
CHAPTER 3 Calculations with Chemical Formulas and Equations MOLECULAR WEIGHT (M. W.) Sum of the Atomic Weights of all atoms in a MOLECULE of a substance. FORMULA WEIGHT (F. W.) Sum of the atomic Weights
SCH 4C1 Unit 2 Problem Set Questions taken from Frank Mustoe et all, "Chemistry 11", McGraw-Hill Ryerson, 2001 1. A small pin contains 0.0178 mol of iron. How many atoms of iron are in the pin? 2. A sample
CHEMISTRY 123-07 Midterm #1 Answer key October 14, 2010 Statistics: Average: 74 p (74%); Highest: 97 p (95%); Lowest: 33 p (33%) Number of students performing at or above average: 67 (57%) Number of students
CHEM 120 Online: Chapter 6 Sample problems Date: 1. To determine the formula mass of a compound you should A) add up the atomic masses of all the atoms present. B) add up the atomic masses of all the atoms
Name: Class: Date: IM Bonding 1) In liquids, the attractive intermolecular forces are. A) very weak compared with kinetic energies of the molecules B) strong enough to hold molecules relatively close together
How much does a single atom weigh? Different elements weigh different amounts related to what makes them unique. What units do we use to define the weight of an atom? amu units of atomic weight. (atomic
35 MOLES ND MOLE CLCULTIONS INTRODUCTION The purpose of this section is to present some methods for calculating both how much of each reactant is used in a chemical reaction, and how much of each product
Physical Science 1 Progression This progression is the about the structure and properties of matter. Matter is composed of material that is too small to be seen, but is understood in terms of the types
TEKS REVIEW 8B Calculating Atoms, Ions, or Molecules Using Moles TEKS 8B READINESS Use the mole concept to calculate the number of atoms, ions, or molecules in a sample TEKS_TXT of material. Vocabulary
Hydrogen Bonds Hydrogen bonds have played an incredibly important role in the history of structural biology. Both the structure of DNA and of protein a-helices and b-sheets were predicted based largely
Moles Balanced chemical equations Molar ratios Mass Composition Empirical and Molecular Mass Predicting Quantities Equations Micro World atoms & molecules Macro World grams Atomic mass is the mass of an
Ca 2+ The contents of this module were developed under grant award # P116B-001338 from the Fund for the Improvement of Postsecondary Education (FIPSE), United States Department of Education. However, those
Chapter 3 Mass Relationships in Chemical Reactions Student: 1. An atom of bromine has a mass about four times greater than that of an atom of neon. Which choice makes the correct comparison of the relative
Lecture 5, The Mole What is a mole? Moles Atomic mass unit and the mole amu definition: 12 C = 12 amu. The atomic mass unit is defined this way. 1 amu = 1.6605 x 10-24 g How many 12 C atoms weigh 12 g?
Lab 11 Sugar or Salt? Ionic and Covalent Bonds TN Standard 2.1: The student will investigate chemical bonding. Have you ever accidentally used salt instead of sugar? D rinking tea that has been sweetened
Determining the Structure of an Organic Compound The analysis of the outcome of a reaction requires that we know the full structure of the products as well as the reactants In the 19 th and early 20 th
1 MOLECULAR MASS AND FORMULA MASS Molecular mass = sum of the atomic weights of all atoms in the molecule. Formula mass = sum of the atomic weights of all atoms in the formula unit. 2 MOLECULAR MASS AND
Chapter 3: Stoichiometry Key Skills: Balance chemical equations Predict the products of simple combination, decomposition, and combustion reactions. Calculate formula weights Convert grams to moles and
4 When sweat evaporates, it cools the skin by absorbing heat from the body. Energy and Matter CAPTER OUTLINE 4.1 Energy 4.2 The Three States of Matter 4.3 Intermolecular Forces 4.4 Boiling Point and Melting
CHAPTER THREE: CALCULATIONS WITH CHEMICAL FORMULAS AND EQUATIONS Part One: Mass and Moles of Substance A. Molecular Mass and Formula Mass. (Section 3.1) 1. Just as we can talk about mass of one atom of
The Mole Concept Ron Robertson r2 c:\files\courses\1110-20\2010 final slides for web\mole concept.docx The Mole The mole is a unit of measurement equal to 6.022 x 10 23 things (to 4 sf) just like there
Chapter 3 Stoichiometry 3-1 Chapter 3 Stoichiometry In This Chapter As you have learned in previous chapters, much of chemistry involves using macroscopic measurements to deduce what happens between atoms
18 electron rule : How to count electrons The rule states that thermodynamically stable transition metal organometallic compounds are formed when the sum of the metal d electrons and the electrons conventionally
Role of Hydrogen Bonding on Protein Secondary Structure Introduction The function and chemical properties of proteins are determined by its three-dimensional structure. The final architecture of the protein
Chem 106 Thursday Feb. 3, 2011 Chapter 13: -The Chemistry of Solids -Phase Diagrams - (no Born-Haber cycle) 2/3/2011 1 Approx surface area (Å 2 ) 253 258 Which C 5 H 12 alkane do you think has the highest
Combinatorial Biochemistry and Phage Display Prof. Valery A. Petrenko Director - Valery Petrenko Instructors Galina Kouzmitcheva and I-Hsuan Chen Auburn 2006, Spring semester COMBINATORIAL BIOCHEMISTRY
Lesson Objectives Students will: Create a physical representation of the autoionization of water using the water kit. Describe and produce a physical representation of the dissociation of a strong acid
CHM111(M)/Page 1 of 5 INTI COLLEGE MALAYSIA A? LEVEL PROGRAMME CHM 111: CHEMISTRY MOCK EXAMINATION: DECEMBER 2000 SESSION SECTION A Answer ALL EIGHT questions. (52 marks) 1. The following is the mass spectrum
Chapter 5 Chemical Quantities and Reactions 5.1 The Mole Collection Terms A collection term states a specific number of items. 1 dozen donuts = 12 donuts 1 ream of paper = 500 sheets 1 case = 24 cans 1
Columbia College Online Campus P a g e 1 CHEM 110 A Chemistry I Early Fall Session (15-51) Monday, August 17 Saturday, October 10, 2015 Course Description Fundamental course in the principles of chemistry.
Chemical Bonds 1. Which of the following is NOT a true compound? a. pure substance b. composed of combinations of atoms c. held together by chemical bonds d. substance that cannot be broken down into simpler
96 Chapter 7: Calculations with Chemical Formulas and Chemical Reactions Chemical reactions are written showing a few individual atoms or molecules reacting to form a few atoms or molecules of products.
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