1 / 64

Organic chemistry for medicine and biology students Chem 2311 Chapter 3 By Prof. Dr.

Explore the fundamentals of organic chemistry focusing on alkenes, alkynes, and hydrocarbons. Learn about the structure, nomenclature, isomerism, and reactions of these important compounds. This comprehensive guide by Prof. Dr. Adel M. Awadallah from the Islamic University of Gaza is essential for students in Chem 2311.

carlgriffin
Download Presentation

Organic chemistry for medicine and biology students Chem 2311 Chapter 3 By Prof. Dr.

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript

  1. Organic chemistry for medicine and biology students Chem 2311 Chapter 3 By Prof. Dr. Adel M. Awadallah Islamic University of Gaza

  2. Alkenes and Alkynes Hydrocarbons(contain only carbon and hydrogen) • Saturated: (Contain only single bonds) Alkanes (CnH2n + 2 ) Cycloalkanes (CnH2n ) b)Unsaturated: contain Alkenes: double bonds (,,,CnH2n) Alkynes: triple bonds ((CnH2n - 2) Aromatic: benzene like compounds

  3. Facts about double and triple bonds

  4. Nomenclature of alkenes and Alkynes • The ending ene is used for alkenes and yne for alkynes • Select the longest chain that includes both carbons of the multiple bond • Number the chain from the end nearest to the multiple bond • Indicate the position of the multiple. Examples

  5. Isomers and common names of simple alkenes

  6. Nomenclature of compounds containing more than one multiple bond • Number from the end nearest to the multiple bond. • If a double and a triple bond are equidistant from he end, the double bond receives the lowest numbers • Example

  7. Compounds containing more than one double bond

  8. Cis-Trans (Z-E) Isomerism in Alkenes If each end of the double bond is attached to two different groups, then the compound exists in two different forms called (Diastereomers; These are non mirror image stereoisomers). If the two groups are identical we distinguish the two isomers by adding the prefix cis (same side) or trans (opposite sides) Example

  9. If the groups attached to the double bond are different, we distinguish the two isomers by adding the prefix Z (same side) or E (opposite sides) depending on the atomic number of the atoms attached to each end of the double bond

  10. Hydrogen is a symmetric reagent

  11. Bromine is a symmetric reagent

  12. Water is unsymmetric reagent

  13. Addition of HBr (Unsymmetric reagent):

  14. Electrophilic addition of HBr to conjugated diens

  15. The Diels –Alder Reaction

  16. Free Radical Polymerization of Ethylene

  17. Examples

  18. Examples

More Related