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Alkene

Organic Chemistry Lecture 9

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Chapter 9 ? 2010, Prentice Hall Organic Chemistry, 7th Edition L. G. Wade, Jr. Alkynes Chapter 9 * Introduction Alkynes contain a triple bond. General formula is CnH2n-2. Two elements of unsaturation for each triple bond. Some reactions resemble the reactions of alkenes, like addition and oxidation. Some reactions are specific to alkynes. Chapter 9 Chapter 9 * Nomenclature: IUPAC Find the longest chain containing the triple bond. Change -ane ending to -yne. Number the chain, starting at the end closest to the triple bond. Give branches or other substituents a number to locate their position. Chapter 9 Chapter 9 * Examples of Nomenclature

Organic Chemistry Lecture 8

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Chapter 8 ? 2010, Prentice Hall Organic Chemistry, 7th Edition L. G. Wade, Jr. Reactions of Alkenes Chapter 8 * Bonding in Alkenes Electrons in pi bond are loosely held. The double bond acts as a nucleophile attacking electrophilic species. Carbocations are intermediates in the reactions. These reactions are called electrophilic additions. Chapter 8 Chapter 8 * Electrophilic Addition Step 1: Pi electrons attack the electrophile. Step 2: Nucleophile attacks the carbocation. Chapter 8 Chapter 8 * Types of Additions Chapter 8 Chapter 8 * Addition of HX to Alkenes Step 1 is the protonation of the double bond. The protonation step forms the most stable carbocation possible. In step 2, the nucleophile attacks the carbocation, forming an alkyl halide.

Organic Chemistry Lecture 7

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Chapter 7 ?2010, Prentice Hall Organic Chemistry, 7th Edition L. G. Wade, Jr. Structure and Synthesis of Alkenes Chapter 7 * Introduction Alkenes are hydrocarbon with carbon-carbon double bonds. Alkenes are also called olefins, meaning ?oil-forming gas?. The functional group of alkenes is the carbon-carbon double bond, which is reactive. Chapter 7 Chapter 7 * Sigma Bonds of Ethylene Chapter 7 Chapter 7 * Orbital Description Sigma bonds around the double-bonded carbon are sp2 hybridized. Angles are approximately 120? and the molecular geometry is trigonal planar. Unhybridized p orbitals with one electron will overlap forming the double bond (pi bond) . Chapter 7 Chapter 7 * Bond Lengths and Angles sp2 hybrid orbitals have more s character than the sp3 hybrid orbitals.

Organic chemistry

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Organic Chemistry Name: _______________________ organic chemistry: the study of carbon-containing compounds -- hydrocarbons: compounds containing only hydrogen and carbon alkanes: contain only single bonds alkenes (olefins): contain at least one C=C double bond alkynes: contain at least one carbon-carbon triple bond aromatic hydrocarbons: benzene-based -- structural isomers: compounds with the same molecular formula but different bonding arrangements e.g., C4H10 Organic Nomenclature Memorize the first ten prefixes. 1 = meth-, 2 = eth-, 3 = prop-, 4 = but-, 5 = pent-, 6 = hex-, 7 = hept-, 8 = oct-, 9 = non-, 10 = dec- NOTE: Hydrocarbon substituent groups use these prefixes and end in –yl. Naming Alkanes

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