CHE-240 Unit 1 Structure and Stereochemistry of Alkanes CHAPTER TWO Terrence P. Sherlock Burlington County College 2004.

Slides:



Advertisements
Similar presentations
Structure and Bonding of Organic Molecules Orbital Theory Hybridization and Geometry Polarity Functional Groups.
Advertisements

Comparing Acid Strengths by Comparing Structures  Look at the stability of the conjugate base. The more stable the conjugate base, the stronger its acid.
Molecular Geometry.
Honors Chemistry Section 6.5.
Properties of compounds
FORMAL CHARGE Formal Charge N :..... N :.... H H NH 2 - Bonded Unbonded Number of All One half of = valence electrons unshared + all shared in the neutral.
Introduction to Organic Molecules & Functional Groups
Classifying Organic Compounds
Drawing Organic Structures Functional Groups Constitutional Isomers
Atomic and Molecular Orbitals l The horizontal rows of the periodic table are called Periods. l Each period represents a different quantum energy level.
Chapter 2 Structure and Properties of Organic Molecules
Organic Functional Groups
© 2013 Pearson Education, Inc. Chapter 2 Lecture Organic Chemistry, 8 th Edition L. G. Wade, Jr. Structure and Properties of Organic Molecules © 2013 Pearson.
UNIT 1 – ORGANIC CHEMISTRY
Basic Chemistry Copyright © 2011 Pearson Education, Inc. Chapter 10 Structures of Solids and Liquids 10.4 Attractive Forces between Particles 1.
Modern Chemistry Chapter 6 Chemical Bonding
Chapter 2 Structure and Properties of Organic Molecules Organic Chemistry, 5 th Edition L. G. Wade, Jr. Jo Blackburn Richland College, Dallas, TX Dallas.
Chapter 2 Structure and Properties of Organic Molecules Organic Chemistry, 6 th Edition L. G. Wade, Jr. Jo Blackburn Richland College, Dallas, TX Dallas.
Families of Carbon Compounds
Geometry of Molecules Significance? Enzymes (metabolic reactions) Drugs Eyesight Sense of smell.
CHE 311 Organic Chemistry I Dr. Jerome K. Williams, Ph.D. Saint Leo University.
Polarity of Molecules 11/18/14 Polar Molecules are molecules which have an uneven distribution of charge. One side of the molecule is negative while.
STRUCTURE Dr. Clower CHEM 2411 Spring 2014 McMurry (8 th ed.) sections , , 20.2, , , , 7.2, 7.6.
Solubility:  Solubility is a characteristic physical property referring to the ability for a given substance, the solute, to dissolve in a solvent. It.
Chapter 3 Drawing Chemical Structures And Classification of Organic Chemistry 2.1 Drawing Chemical Structures 2.2 Classification of Organic Chemistry.
Chapter 2 Structure and Properties of Organic Molecules Organic Chemistry, 5 th Edition L. G. Wade, Jr.
Chapter 1 Organic Chemistry Chemistry 20. Organic Compounds.
Chapter 6 Preview Objectives Molecular Geometry VSEPR Theory
Covalent Bonding Chapter The Covalent Bond  In order for an atom to gain stability, it can gain, lose, or share electrons.  Atoms that share.
DRAWING ORGANIC STRUCTURES FUNCTIONAL GROUPS CONSTITUTIONAL ISOMERS Dr. Clower CHEM 2411 Spring 2014 McMurry (8 th ed.) sections 1.12, 3.1, 3.2.
CHAPTER 23 ORGANIC CHEMISTRY. The Nature of Organic Molecules Carbon is tetravalent. It has four outer-shell electrons (1s 2 2s 2 2p 2 ) and forms four.
Chapter 21  Functional Groups  Functional group families are characterized by the presence of a certain arrangement of atoms called a functional group.
FUNCTIONAL GROUPS. A functional group is a cluster of atoms within a molecule that have specific reactivity patterns Compounds with the same functional.
Molecular Bonding Unit 5. Covalent Bonds Sharing pairs of electrons Sharing pairs of electrons Covalent bonds are the inter-atomic attraction resulting.
Chapter 1-Continue Introduction to Organic Chemistry.
Organic Chemistry. Homologous Series A grouping of organic compounds based on their composition and properties A series has: A general formula The same.
Intermolecular Forces
Functional Groups. Ether General formula: R-O-R or R-O-R’ where R or R’ may be an alkyl Name ends with ether.
© Houghton Mifflin Harcourt Publishing Company Molecular Geometry The properties of molecules depend not only on the bonding of atoms but also on molecular.
1 Section 8.1The Covalent Bond Section 8.2 Naming Molecules Section 8.3 Molecular Structures Section 8.4 Molecular Shapes (Hybridization and VSEPR model)
Ch. 8 Covalent Bonding Pre AP Chemistry. I. Molecular Compounds  A. Molecules & Molecular Formulas  1. Another way that atoms can combine is by sharing.
Structure and Properties of Organic Molecules
Structure and Properties of Organic Molecules Adapted from Chapter 2 of Organic Chemistry by L. G. Wade, Jr. Highland Hall Biochem Block Handout #2.
Chapter 2 Copyright © 2010 Pearson Education, Inc. Organic Chemistry, 7 th Edition L. G. Wade, Jr. Structure and Properties of Organic Molecules.
1 Organic Chemistry MDL233 Chapter 2 BY Mahwash Hafeez.
© 2014 Pearson Education, Inc. Chad Snyder, PhD Grace College Chapter 2 Lecture Organic Chemistry, 9 th Edition L. G. Wade, Jr. Acids and Bases; Functional.
Acids and Bases Functional Groups Polarity Intermolecular Forces Acids and Bases Functional Groups.
Chapter 2 Families of Carbon Compounds. Basic Definitions Hydrocarbons- Compounds containing only carbon and hydrogen. Alkanes- hydrocarbons that contain.
Acids and Bases: Functional Groups (Part 2)
Lecture: 5 Properties, structures, existence and synthesis/perparation
Chapter 24From Petroleum to Pharmaceuticals
Chapter 6 Preview Objectives Molecular Geometry VSEPR Theory
Chapter 6 –The Shape of Molecules
Chemical Bonding II: Molecular Geometry and Hybridization of Atomic Orbitals Chapter 10 Copyright © The McGraw-Hill Companies, Inc.  Permission required.
Chemical Bonding II: Molecular Geometry and Hybridization of Atomic Orbitals Chapter 10 Copyright © The McGraw-Hill Companies, Inc.  Permission required.
Chapter 6 Molecular Geometry
Acids and Bases Functional Groups
Bonding and Properties
Molecular Geometry.
Structure and Properties of Organic Molecules
Valence Shell Electron Pair Repulsion Theory
Molecular Shapes and Hybrid Orbitals
Types of Covalent Bonds
Introduction Organic chemistry is the study of molecules that contain carbon Carbon is special because: - can form 4 strong covalent bonds - can bond with.
CHE-240 Unit 1 Structure and Stereochemistry of Alkanes CHAPTER ONE
Chapter 10 Properties of Solids and Liquids
Ch. 6.5 Molecular Structure
Chapter 6 Preview Multiple Choice Short Answer Extended Response
Hybridization of atoms
Hybridized Atomic Orbitals
Presentation transcript:

CHE-240 Unit 1 Structure and Stereochemistry of Alkanes CHAPTER TWO Terrence P. Sherlock Burlington County College 2004

Chapter 22 Multiple Bonds A double bond (2 pairs of shared electrons) consists of a sigma bond and a pi bond. A triple bond (3 pairs of shared electrons) consists of a sigma bond and two pi bonds. =>

Chapter 23 Molecular Shapes Bond angles cannot be explained with simple s and p orbitals. Use VSEPR theory. Hybridized orbitals are lower in energy because electron pairs are farther apart. Hybridization is LCAO within one atom, just prior to bonding. =>

Chapter 24 sp Hybrid Orbitals 2 VSEPR pairs Linear electron pair geometry 180° bond angle =>

Chapter 25 sp 2 Hybrid Orbitals 3 VSEPR pairs Trigonal planar e - pair geometry 120° bond angle =>

Chapter 26 sp 3 Hybrid Orbitals 4 VSEPR pairs Tetrahedral e - pair geometry 109.5° bond angle =>

Chapter 27 Sample Problems Predict the hybridization, geometry, and bond angle for each atom in the following molecules: Caution! You must start with a good Lewis structure! NH 2 CH 3 -C  C-CHO =>

Chapter 28 Bond Dipole Moments are due to differences in electronegativity. depend on the amount of charge and distance of separation. In debyes,  x  (electron charge) x d(angstroms) =>

Chapter 29 Molecular Dipole Moments Depend on bond polarity and bond angles. Vector sum of the bond dipole moments. Lone pairs of electrons contribute to the dipole moment. =>

Chapter 210 Intermolecular Forces Strength of attractions between molecules influence m.p., b.p., and solubility; esp. for solids and liquids. Classification depends on structure.  Dipole-dipole interactions  London dispersions  Hydrogen bonding =>

Chapter 211 Dipole-Dipole Forces Between polar molecules Positive end of one molecule aligns with negative end of another molecule. Lower energy than repulsions, so net force is attractive. Larger dipoles cause higher boiling points and higher heats of vaporization. =>

Chapter 212 Dipole-Dipole =>

Chapter 213 London Dispersions Between nonpolar molecules Temporary dipole-dipole interactions Larger atoms are more polarizable. Branching lowers b.p. because of decreased surface contact between molecules. =>

Chapter 214 Dispersions =>

Chapter 215 Hydrogen Bonding Strong dipole-dipole attraction Organic molecule must have N-H or O-H. The hydrogen from one molecule is strongly attracted to a lone pair of electrons on the other molecule. O-H more polar than N-H, so stronger hydrogen bonding =>

Chapter 216 H Bonds =>

Chapter 217 Boiling Points and Intermolecular Forces =>

Chapter 218 Solubility Like dissolves like Polar solutes dissolve in polar solvents. Nonpolar solutes dissolve in nonpolar solvents. Molecules with similar intermolecular forces will mix freely. =>

Chapter 219 Hydrocarbons Alkane: single bonds, sp 3 carbons Cycloalkane: carbons form a ring Alkene: double bond, sp 2 carbons Cycloalkene: double bond in ring Alkyne: triple bond, sp carbons Aromatic: contains a benzene ring =>

Chapter 220 Compounds Containing Oxygen Alcohol: R-OH Ether: R-O-R ' Aldehyde: RCHO Ketone: RCOR ' =>

Chapter 221 Carboxylic Acids and Their Derivatives Carboxylic Acid: RCOOH Acid Chloride: RCOCl Ester: RCOOR ' Amide: RCONH 2 =>

Chapter 222 Compounds Containing Nitrogen Amines: RNH 2, RNHR ', or R 3 N Amides: RCONH 2, RCONHR, RCONR 2 Nitrile: RCN =>

Chapter 223 POWER POINT IMAGES FROM “ORGANIC CHEMISTRY, 5 TH EDITION” L.G. WADE ALL MATERIALS USED WITH PERMISSION OF AUTHOR PRESENTATION ADAPTED FOR BURLINGTON COUNTY COLLEGE ORGANIC CHEMISTRY COURSE BY: ANNALICIA POEHLER STEFANIE LAYMAN CALY MARTIN