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Bonding
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Electrons
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Electron Configurations
Electron Configurations are a short hand way to show where all the electrons are located in an atom
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How to Write and Electron Configuration
Determine the number of electrons For a neutral atom = the atomic number For an ion= atomic number - the oxidation number Fill the orbitals according to the orbital filling diagram until all electrons have been placed
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Examples Lithium: Phosphorous: Chlorine: Cl-1: Mg+2:
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Valence Electrons Valence electrons are the electrons located in the outermost energy level of the atom The number of valence electrons can be predicted by the position on the periodic table Highlight the valence electrons in the examples above
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Predicting Valence Electrons
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Lewis Dot Structures Diagrams that use the chemical symbol and dots to represent the valence electrons for an atom How to draw Lewis Structure for an atom: Write the symbol Place one dot on each side of the symbol to represent the valence electrons until all valence electrons are placed
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Examples: Lithium Phosphorous Chlorine Magnesium Argon
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The Octet Rule Atoms will loose, gain, or share electrons in order to acquire a full outer shell of 8 valence electrons Exceptions include those of period 1, Lithium, Beryllium, and Boron which prefer to have a full outer shell of 2 Once the atoms has bonded in a way to provide a full outer shell, we say it has a stable octet
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Electronegativity Electronegativity is the attraction an atom has for electrons in a chemical bond The electronegativity of an atom determines what will happen to its electrons when bonding
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Ionic Compounds Involve a transfer of electrons from a metal to a nonmetal Results in a metal cation and an a nonmetal anion that then bond in order to neutralize the charge between the two Ionic compounds have an electronegativity difference greater than or equal to 2.0
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Covalent Compounds Also known as Molecular Compounds or Molecules
Involve a sharing of electrons between two nonmetals In a covalent compound there is no neutralization of charge Atoms share electrons so that all the atoms can obtain a stable octet Covalent compounds have an electronegativity difference less than 2.0
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Lewis Structure for Covalent Compounds
Count the total number of valence electrons for ALL atoms in the molecule If the molecule is charged subtract the oxidation number Draw the skeletal structure for the molecule Put the most electronegative or single atom in the center Hydrogen is always on the outside Draw a single bond between each of the atoms in the compound (two dots, or one solid line) Subtract the bonding electrons from the total number Place the remaining electrons to fill the octets of the outer atoms Place any remaining electron pairs on the central atom If the central atom does not have a complete octet move atoms to form multiple bonds until it does
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Simple Covalent Compounds
Water: H2O Methane: CH4
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The Lewis Challenge Draw the Lewis Structure for the following compounds based on the conditions below: You must satisfy the octet rule for all atoms involved. Some atoms may share more than one pair of electrons. All valence electrons for all atoms must be accounted for. F2 N2 HCN
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Covalent Compounds with Multiple Bonds
Single Bonds- two atoms share one pair of electrons Double Bonds- two atoms share two pairs of electrons Triple Bonds- two atoms share three pairs of electrons
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Examples Carbon Dioxide: CO2 Nitrogen: N2
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Covalent Compounds with Charges (Polyatomic Ions)
For a charged covalent compound, draw the structure the same way then place the entire structure in brackets with the charge on the outside
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Examples Nitrate: NO3-1 Carbonate: CO3 -2
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VSEPR and Molecular Geometry
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VSEPR VSEPR stands for valence shell electron pair repulsion
A model for predicting the geometry of molecules based on the arrangement of atoms that minimizes the repulsion of bonding and nonbonding pairs of electrons
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Bonding pairs= pairs of electrons that are participating in a bond
Nonbonding pairs= pairs of electrons not participating in a bond (also sometimes called lone pairs)
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Predicting Molecular Geometry
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Linear Compound Dot Diagram VSEPR Model HCl
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Bent/Angular Compound Dot Diagram VSEPR Model H2O
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Trigonal Planar Compound Dot Diagram VSEPR Model AlCl3
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Trigonal Pyramidal Compound Dot Diagram VSEPR Model NF3
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Tetrahedral Compound Dot Diagram VSEPR Model CH4
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Molecular Polarity
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Polar Molecules Polar molecules are molecules in which electrons are not shared evenly The charges referred to in a polar molecule are much weaker than those in an ionic compound
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Polar molecules are sometimes called a dipole because they have two ends with slightly different charges A slightly negative end Labeled δ- Always associated with the more electronegative atom A slightly positive end Labeled δ+
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Polarity can be determined by Electron Placement
Polarity can be predicted based on the number of bonding and nonbonding pairs Any molecule with a high concentration of nonbonding electrons around an electronegative atom will be a polar molecule (Delete the line that says: “polar molecules will be one of three molecular geometries”)
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Examples Compound HCl H2O NH3 CHCl3 Dot Diagram Molecular Geometry
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Bond Polarity Nonpolar molecules can still have polarity in their bonds The more electronegative atom will be where the electrons spend more of their time, giving that end of the bond a slightly negative charge Bond polarity can be calculated using electronegativity.
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Bond Polarity Example: Methane
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Intra and Intermolecular Forces
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Intramolecular Forces
Intra= inside Intramolecular forces are the strong forces within a chemical bond
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Ionic Bonds Electrostatic attractions between a cation (+ ion) and an anion (- ion) Results in the formation of a crystal lattice, where every cation is surrounded by anions and every anion is surrounded by cations Ionic bonds are the strongest chemical bonds
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Crystal Lattice Illustration
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Metallic Bonds Attractions between metal cations and delocalized electrons Results in a network similar to the ionic crystal lattice Metallic bonds are slightly weaker than ionic bonds
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Electron Sea Model
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Covalent Bonds Result in the formation of molecules
forces between the electrons of one atom and the nucleus of another Result in the formation of molecules Slightly weaker than metallic bonds, with the exception of the covalent bonds found in network covalent compounds (which are stronger than ionic bonds)
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Intermolecular Forces
Inter= between Intermolecular forces are the forces between molecules They are ONLY found in covalent compounds, in between molecules
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Dipole-Dipole Interactions
Weak attractions between the δ- end of one molecule and the δ- end of another Example: H-Cl
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Hydrogen Bonding Dipole interactions between hydrogen of one molecule and the nitrogen, oxygen, or fluorine of another Example: Water
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Dispersion Forces Attractions between nonpolar compounds, between bonding electrons of one molecule and the nucleus of atoms in another molecule Example: Methane
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Strength of Intermolecular Forces
Ionic Metallic Covalent Hydrogen Bonding Dipole-Dipole Interactions Dispersion Forces DECREASES
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Properties and Strengths of Compounds
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Types of Compounds Network Covalent- compounds that are composed of atoms covalently bonded to each other multiple times Examples: diamond, sand
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Ionic- compounds that result from the attraction of positive ions (cations) to negative ions (anions) Examples: NaCl Mg(OH)2
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Polar Covalent Compounds- compounds where electrons are shared unevenly
Example: water
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Non-Polar Covalent Compounds-compounds where electrons are shared evenly
Example: Methane
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Strengths of Compounds
Type of Compound Relative Strength Types of Forces MP and BP Solubility Conductivity Network Covalent Ionic Metallic Polar Covalent Non-Polar Covalent
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Strengths of Compounds
Type of Compound Relative Strength Types of Forces MP and BP Solubility Conductivity Network Covalent Only covalent bonds highest Not soluble in anything No Ionic Ionic bonds Soluble in water and polar solvents Yes Metallic Metallic bonds N/A Polar Covalent Covalent bonds, hydrogen bonds, dipole interactions Non-Polar Covalent Covalent bonds, dispersion forces lowest Soluble in nonpolar solvents only
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Organic Molecules
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Defining Organic Molecules
All organic molecules contain a large amount of carbon Monomers- single organic subunits Polymers- long chains of monomers Importance of Polymers Biological Molecules- DNA, proteins, carbohydrates, lipids Industry- plastics
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Alkanes Most basic organic compounds Also called hydrocarbonds
Made of only carbon and hydrogen with single bonds General Formula for alkanes: CnH2n+2
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Names and Formulas for Alkanes
CH4 C6H14 C2H6 C7H16 C3H8 C8H18 C4H10 C9H20 C5H12 C10H22
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Other Organic Compounds
Variation on alkanes with the addition of functional groups Functional Group- a group of molecules that when added to an alkane base, changes the physical and chemical properties of the compound
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Alkene Functional Group: carbon-carbon double bond
Properties: Stronger than alkanes
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Alkyne Functional Group: carbon-carbon triple bond
Properties: stronger than alkanes and alkenes; always linear
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Alcohols Functional Group: hydroxyl group
Properties: Makes the molecule polar
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Carboxylic Acids Functional Group: carboxyl group
Properties: polarity, acidic properties
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