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Cyclohexane conformation

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 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.

Stereo chemistry of organic compounds

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Organic Chemistry Stereochemistry of Organic Compounds Dr. Anita Tandon University of Delhi Delhi -110007 CONTENTS Structural Isomers Stereoisomers Conformational Isomers Configurational Isomers (i) Optical isomers (a) Compound with one Asymmetric Carbon Atom (b) Compound with more than one Asymmetric Carbon Atom (c) Compound with no Asymmetric Carbon Atom (d) Elements of Symmetry (e) Properties of Enantiomers (f) Relative Configuration (g) Absolute Configuration (h) Fischer?s Plane Projection Diagram (i) Optical inactivity in compounds having Chiral Carbon Atom (ii) Geometrical Isomers (a) E&Z system of nomenclature (b) Properties of Geometrical Isomers
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