Haloalkane
Organic Chemistry Lecture 11b
Organic Chemistry Lecture 8
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 9
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
Organic Chemistry Lecture 7
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 Lecture 6
Chapter 6 Organic Chemistry, 7th Edition L. G. Wade, Jr. Alkyl Halides: Nucleophilic Substitution and Elimination ?2010, Prentice Hall Chapter 6 * Classes of Halides Alkyl halides: Halogen, X, is directly bonded to sp3 carbon. Vinyl halides: X is bonded to sp2 carbon of alkene. Aryl halides: X is bonded to sp2 carbon on benzene ring. C C H H H C l vinyl halide C H H H C H H B r alkyl halide I aryl halide Chapter 6 Chapter 6 * Polarity and Reactivity Halogens are more electronegative than C. Carbon?halogen bond is polar, so carbon has partial positive charge. Carbon can be attacked by a nucleophile. Halogen can leave with the electron pair. Chapter 6 Chapter 6 * IUPAC Nomenclature Name as haloalkane.
Need Help?
We hope your visit has been a productive one. If you're having any problems, or would like to give some feedback, we'd love to hear from you.
For general help, questions, and suggestions, try our dedicated support forums.
If you need to contact the Course-Notes.Org web experience team, please use our contact form.
Need Notes?
While we strive to provide the most comprehensive notes for as many high school textbooks as possible, there are certainly going to be some that we miss. Drop us a note and let us know which textbooks you need. Be sure to include which edition of the textbook you are using! If we see enough demand, we'll do whatever we can to get those notes up on the site for you!