1. Chapter 22 Amines

2. 22.1 Amine Nomenclature

3. Alkylamine N attached to alkyl group Arylamine N attached to aryl group Primary, secondary, or tertiary determined by number of carbon atoms directly attached to nitrogen Classification of Amines

4. Examples: some primary alkylamines CH 3 CHCH 2 CH 2 CH 3 NH 2 (RNH 2 : one carbon directly attached to N) CH 3 CH 2 NH 2 NH 2 ethylamine or ethanamine cyclohexylamine or cyclohexanamine 1-methylbutylamine or 2-pentanamine

5. Examples: some primary arylamines (ArNH 2 : one carbon directly attached to N) p-fluoroaniline 5-bromo-2-ethylaniline NH 2 F Br CH 2 CH 3

6. Examples CH 3 NHCH 2 CH 3 N-methylethylamine NHCH 2 CH 3 NO 2 Cl 4-chloro-N-ethyl-3-nitroaniline CH 3 N N,N-dimethylcycloheptylamine

7. A nitrogen with four substituents is positively charged and is named as a derivative of ammonium ion (NH 4 + ). Ammonium Salts CH 3 NH 3 + Cl– methylammonium chloride N CH 3 H CH 2 CH 3 + CF 3 CO 2 – N-ethyl-N-methylcyclopentylammonium trifluoroacetate

8. When all four atoms attached to N are carbon, the ion is called a quaternary ammonium ion and salts that contain it are called quaternary ammonium salts. Ammonium Salts + CH 2 N CH 3 I – benzyltrimethylammonium iodide

9. 22.2 Structure and Bonding

10. 147 pm 106° 112° Alkylamines

11. Most prominent feature is high electrostatic potential at nitrogen. Reactivity of nitrogen lone pair dominates properties of amines. Alkylamines

12. Compare geometry at N of methylamine, aniline, and formamide. sp 3 sp 2 Geometry at N Pyramidal geometry at sp 3 -hybridized N in methylamine. Planar geometry at sp 2 -hybridized N in formamide. C O NH 2 H C H H H

13. Compare geometry at N of methylamine, aniline, and formamide. sp 3 sp 2 Geometry at N Pyramidal geometry at sp 3 -hybridized N in methylamine. Planar geometry at sp 2 -hybridized N in formamide.

14. Angle that the C—N bond makes with bisector of H—N—H angle is a measure of geometry at N. sp 3 sp 2 Geometry at N ~125° 180° Note: this is not the same as the H—N—H bond angle

15. Angle that the C—N bond makes with bisector of H—N—H angle is a measure of geometry at N. sp 3 sp 2 Geometry at N ~125° 180° 142.5°

16. Geometry at N in aniline is pyramidal; closer to methylamine than to formamide. Geometry at N 142.5°

17. 142.5° Hybridization of N in aniline lies between sp 3 and sp 2. Lone pair of N can be delocalized into ring best if N is sp 2 and lone pair is in a p orbital. Lone pair bound most strongly by N if pair is in an sp 3 orbital of N, rather than p. Actual hybridization is a compromise that maximizes binding of lone pair.

18. Electrostatic Potential Maps of Aniline Nonplanar geometry at N. Region of highest negative potential is at N. Planar geometry at N. High negative potential shared by N and ring. Figure 22.3 (page 862)

19. 22.3 Physical Properties

20. Amines are more polar and have higher boiling points than alkanes; but are less polar and have lower boiling points than alcohols. Physical Properties CH 3 CH 2 CH 3 CH 3 CH 2 NH 2 CH 3 CH 2 OH dipole moment (  ): boiling point: 0 D 1.2 D 1.7 D -42°C17°C78°C

21. Boiling points of isomeric amines decrease in going from primary to secondary to tertiary amines. Primary amines have two hydrogens on N capable of being involved in intermolecular hydrogen bonding. Secondary amines have one. Tertiary amines cannot be involved in intermolecular hydrogen bonds. Physical Properties CH 3 CH 2 NHCH 3 CH 3 CH 2 CH 2 NH 2 (CH 3 ) 3 N boiling point: 50°C34°C3°C