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Chemistry

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Organic Chapter 7 ppt

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Chapter 7 Structure and Synthesis of Alkenes Jo Blackburn Richland College, Dallas, TX Dallas County Community College District ? 2006, Prentice Hall Organic Chemistry, 6th Edition L. G. Wade, Jr. Chapter 7 * Introduction Hydrocarbon with carbon-carbon double bonds Sometimes called olefins Term derived from olefiant gas meaning ?oil-forming gas? Originates with early experiments and the oily appearance of alkene derivatives Chapter 7 Chapter 7 * Characteristics Among most important industrial compounds and found in many plants and animals Ethylene ? a.k.a. ethene largest volume industrial organic compound used to make polyethylene and others Pinene ? major component of turpentine ? paint solvent distilled from extracts of evergreen trees Chapter 7 Chapter 7 *

Organic Chapter 6 ppt

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Chapter 6 Alkyl Halides: Nucleophilic Substitution and Elimination Organic Chemistry, 6h Edition L. G. Wade, Jr. Chapter 6 * Classes of Halides Alkyl: Halogen, X, is directly bonded to sp3 carbon. Most reactions result from breaking of this bond. C ? X bond is polar (EN difference) C is slightly positive ? electrophilic (can be attacked by nucleophile) X can leave with electrons ? elimination X can be replaced with another functional group ? substitution Chapter 6 Chapter 6 * Classes of Halides Examples: CHCl3 ? chloroform (solvent) CHClF2 ? freon-22 (refrigerant) CCl3 ? CH3 ? 1,1,1-trichloroethane (cleaning fluid) CF3 ? CHClBr ? halothane (nonflammable anesthetic) Chapter 6 Chapter 6 * Classes of Halides Vinyl: X is bonded to sp2 carbon of alkene. Examples:

Organic Chapter 5 ppt

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Chapter 5 Stereochemistry Organic Chemistry, 6th Edition L. G. Wade, Jr. Chapter 5 * Summary of Isomers => Chapter 5 Chapter 5 * Stereochemistry The study of 3-D structure of molecues. Recall the 2 different types of isomers: Constitutional Stereoisomers Chapter 5 Chapter 5 * Stereoisomers Same bonding sequence. Different arrangement in space. Example: HOOC-CH=CH-COOH has two geometric (cis-trans) isomers: o o => Chapter 5 Chapter 5 * Chirality ?Handedness?: right glove doesn?t fit the left hand. Mirror-image object is different from the original object. Relationship ? the objects are nonsuperimposable (nonidentical) mirror images. Chapter 5 Chapter 5 * Chirality in Molecules The cis isomer is achiral (?not handed? or identical with its mirror image).

Organic Chapter 4 ppt

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Chapter 4 The Study of Chemical Reactions Organic Chemistry, 6th Edition L. G. Wade, Jr. Chapter 4 * Introduction Reactants ? Products: overall reaction. Mechanism: complete step-by-step description of exactly which bonds break and form in what order to give observed products To learn more about a reaction: Thermodynamics Kinetics. => Chapter 4 Chapter 4 * Thermodynamics study of energy changes provides an opportunity to: compare stability of reactants and products predict which compounds are favored Kinetics study of reaction rates, determining which products form the fastest helps predict how the rate will change if conditions are changed Chapter 4 Chapter 4 * Chlorination of Methane

Organic Chapter 3 ppt

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Chapter 3 Structure and Stereochemistry of Alkanes Organic Chemistry, 6th Edition L. G. Wade, Jr. Chapter 3 * Classification Review Chapter 3 Chapter 3 * Alkane Formulas All C-C single bonds Saturated with hydrogens Ratio: CnH2n+2 Alkane homologs: CH3(CH2)nCH3 Same ratio for branched alkanes => Chapter 3 Chapter 3 * Common Names Isobutane, ?isomer of butane? Isopentane, isohexane, etc., methyl branch on next-to-last carbon in chain. Neopentane, most highly branched Five possible isomers of hexane, 18 isomers of octane and 75 for decane! => Chapter 3 Chapter 3 * Alkane Examples => Chapter 3 Chapter 3 * IUPAC Names Find the longest continuous carbon chain.

Organic Chapter 2 ppt

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Chapter 2 Structure and Properties of Organic Molecules Organic Chemistry, 6th Edition L. G. Wade, Jr. Chapter 2 * Sigma Bonding Electron density lies between the nuclei. A bond may be formed by s-s, p-p, s-p, or hybridized orbital overlaps. => Chapter 2 Chapter 2 * Pi Bonding Pi bonds form after sigma bonds. Sideways overlap of parallel p orbitals. => Chapter 2 Chapter 2 * 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 2 Chapter 2 * Molecular Shapes Bond angles cannot be explained with simple s and p orbitals. Use VSEPR theory.

Organic Chapter 1 ppt

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Chapter 1 Introduction and Review Organic Chemistry, 6th Edition L. G. Wade, Jr. Chapter 1 * Definitions Old: ?derived from living organisms? New: ?chemistry of carbon compounds? From inorganic to organic, vitalism and W?hler, 1828 => Chapter 1 Chapter 1 * Atomic Structure Atoms: protons, neutrons, and electrons. The number of protons determines the identity of the element. Some atoms of the same element have a different number of neutrons. These are called isotopes. Example: 12C, 13C, and 14C => Chapter 1 Chapter 1 * Electronic Structure Electrons: outside the nucleus, in orbitals. Electrons have wave properties. Electron density is the probability of finding the electron in a particular part of an orbital.

Atomic Radius

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Atomic Radius: The atomic radius is the size of the atom of an element. The values decrease. Yes, they both decrease. The atomic radius increases. Yes, but they increase at a slower rate. Ionic Radius: An atom becomes a cation when an atom loses electrons in a reaction. An atom becomes an anion when it gains electrons in a reaction. The cations? values decrease. The anion?s values also decrease. Yes, their trends are the same. The ionic radius value increases. Yes, they also increase. Electronegativity: Electronegativity is the measurement of an element?s tendency to react with electrons in a chemical bond. The values greatly increase. Yes, they both increase. The values slowly decrease. No, because only one number in group 18 is plotted.

lab9

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lab8

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