1. © Prentice Hall 2001Chapter 21 Nomenclature of Alkyl Substituents If a Hydrogen is replaced by a halogen, the compound is an alkyl halide

2. © Prentice Hall 2001Chapter 22 Nomenclature of Alkyl Halides Common name - Name the alkyl group first, followed by the name of the halogen expressed as an -ide name

3. © Prentice Hall 2001Chapter 23 Nomenclature of Alkyl Halides IUPAC name - The halogen is treated as a substituent

4. © Prentice Hall 2001Chapter 24 Nomenclature of Ethers Common name - Name(s) of alkyl group(s) listed first followed by the word “ether”

5. © Prentice Hall 2001Chapter 25 Nomenclature of Ethers IUPAC name - The smaller alkyl group is converted to an “alkoxy” name and used as a substituent

6. © Prentice Hall 2001Chapter 26 Nomenclature of Alkyl Substituents If a hydrogen of an alkane is replaced by an OH group, the compound is an alcohol

7. © Prentice Hall 2001Chapter 27 Nomenclature of Alcohols Alcohols are classified as primary, secondary or tertiary

8. © Prentice Hall 2001Chapter 28 Nomenclature of Alcohols Common name - Name of the Alkyl group followed by the word “alcohol”

9. © Prentice Hall 2001Chapter 29 Nomenclature of Alcohols IUPAC name - The OH group is a site of reactivity (a functional group) Functional group is denoted by the suffix, “ol” methanol ethanol

10. © Prentice Hall 2001Chapter 210 IUPAC Nomenclature of Alcohols 1.Parent Hydrocarbon is the longest continuous chain that contains the OH 2.Number the chain in direction that gives functional group the lowest number 3.If both a substituent and a functional group are present, the functional group gets the lower number

11. © Prentice Hall 2001Chapter 211 IUPAC Nomenclature of Alcohols 4.If the functional group gets the same number when counted from both directions, use direction which gives the substituent the lower number 5.If there is more than one substituent, cite substituents in alphabetical order

12. © Prentice Hall 2001Chapter 212 IUPAC Nomenclature of Alcohols System is summarized as [Substituent] [Parent Hydrocarbon] [Functional Group]

13. © Prentice Hall 2001Chapter 213 Nomenclature of Alkyl Substituents If a hydrogen is replaced by an NH 2, the compound is an amine

14. © Prentice Hall 2001Chapter 214 Nomenclature of Amines Common name - Name of the Alkyl group(s) (in alphabetical order) followed by the syllable “amine” The whole name is a single word methylamine methylpropylamine

15. © Prentice Hall 2001Chapter 215 Nomenclature of Amines IUPAC name - The NH 2 group is a site of reactivity (a functional group) Functional group is denoted by the suffix, “amine” Final “e” of longest alkane group replaced by suffix “amine” 1-butanamine butan-1-amine

16. © Prentice Hall 2001Chapter 216 Nomenclature of Amines Amines are classified as primary, secondary or tertiary depending on number of alkyl groups bonded to the nitrogen

17. © Prentice Hall 2001Chapter 217 Nomenclature of Amines In some compounds there are four alkyl groups bonded to a nitrogen Such compounds must be salts because it is impossible to have four bonds to nitrogen without having developed a positive charge These are quaternary ammonium salts

18. © Prentice Hall 2001Chapter 218 Structures of Alkyl Halides, Alcohols, Ethers, & Amines

19. © Prentice Hall 2001Chapter 219 Structures of Alkyl Halides, Alcohols, Ethers, & Amines

20. © Prentice Hall 2001Chapter 220 Properties of Alkyl Halides, Alcohols, Ethers, & Amines Three physical properties are compared for these classes of compounds, 1.) boiling point, 2.) melting point, and 3.) solubility Boiling point increases as the number of carbons in a hydrocarbon increases As branching increases boiling point decreases

21. © Prentice Hall 2001Chapter 221 Properties of Alkyl Halides, Alcohols, Ethers, & Amines Boiling point principally is a function of intermolecular attractions of which there are basically two kinds: 1.) dipole-dipole, and 2.) induced dipole-induce dipole Dipole-dipole interactions stronger A particularly strong dipole-dipole interaction is the hydrogen bond (requires a hydrogen atom bonded to a nitrogen, oxygen or fluorine atom)

22. © Prentice Hall 2001Chapter 222 Properties of Alkyl Halides, Alcohols, Ethers, & Amines For alkanes, there are only induced dipole-induced dipole interactions (also known as van der Waals forces or London forces) van der Waals forces are a function of surface area

23. © Prentice Hall 2001Chapter 223 Induced Dipole-Induced Dipole Interactions

24. © Prentice Hall 2001Chapter 224 Hydrogen Bonding: Strong Dipole-Dipole Interactions

25. © Prentice Hall 2001Chapter 225 Dipole-dipole Interactions Particularly important for alcohols and amines Ethers and alkyl halides have dipole moments, but their intermolecular attractions are not as strong as hydrogen bonds

26. © Prentice Hall 2001Chapter 226 Comparative Boiling Points

27. © Prentice Hall 2001Chapter 227 Melting Points Melting point are a function of: intermolecular attractions packing in the crystalline state

28. © Prentice Hall 2001Chapter 228 Solubility The more carbons that are present, the less soluble an organic compound is in water