Presentation on theme: "Unit 4 Alkyl Halides: Nucleophilic Substitution and Elimination Reactions."— Presentation transcript:
Unit 4 Alkyl Halides: Nucleophilic Substitution and Elimination Reactions
Nomenclature of Alkyl Halides Apply the same rules you learned for the alkanes. IUPAC: Name the halogen as a substituent. bromoethane Common name: The alkyl group is named as the substituent. Ethyl bromide CH 3 CH 2 Br
Nomenclature of Alkyl Halides 3-(iodomethyl)pentane 4-(2-fluoroethyl)heptane
Nomenclature of Alkyl Halides An alkyl halide has a halogen bonded to an sp 3 C. Methyl halides, CH 3 X: the sp 3 C is bonded only to H atoms. X denotes a halogen: F, Cl, Br, I. Primary (1°) halides, RCH 2 X: the sp 3 C is bonded to one other C atom. CH 3 Br CH 3 CH 2 Br
Nomenclature of Alkyl Halides A vicinyl dihalide has two halogens bonded to neighboring sp 3 C atoms. A geminal dihalide has two halogens on the same sp 3 C.
Nomenclature of Alkyl Halides A allylic halogen is one that is bonded to the sp 3 C atom immediately next to a double bond. FYI: The allylic position can be occupied by a substituent other than a halogen.
Nomenclature of Other Halides A benzylic halide has a halogen bonded to an sp 3 C substituent of benzene.
Nomenclature: Nitro, Phenyl A benzene ring as a substituent is called phenyl, -C 6 H 5. Another substituent to know is the nitro group, -NO 2. trans-9-phenyl-2-methylundec-3-ene TNT
Uses of Alkyl Halides Solvents 1,1,1-trichloroethane and methylene chloride Starting materials for syntheses. Anesthetics Halothane Freons Pesticides DDT, lindane (lice), chlordane (termites)
C-X is a Polar Bond Polar bonds have dipole moments which are proportional to both partial charge and bond length. Partial charge increases with electronegativity: I
"name": "C-X is a Polar Bond Polar bonds have dipole moments which are proportional to both partial charge and bond length.",
"description": " Partial charge increases with electronegativity: I
C-X is a Polar Bond E.N.bond length partial charge dipole moment F4.01.380.231.51 D Cl3.21.780.181.56 D Br3.01.940.161.48 D I18.104.22.168.29 D for comparisondipole moment C-H0.3 D N-H1.31 D O-H1.53 D C=O2.4 D C≡NC≡N3.6 D
Intermolecular Forces in Alkyl Halides The strongest intermolecular force in alkyl halides is the London force (instantaneous dipole-induced dipole). This force increases with molecular weight and with surface area. Since the C-X bond is polar, there will also be a contribution from the dipole- dipole attraction.
Physical Properties of Alkyl Halides - Boiling Points Here the surface area has more effect than the C-X dipole. Since atomic size increases down the halogen group, boiling points will, too, if the alkyl part of the compound is the same. For compounds with similar molecular weights, branched compounds will have lower boiling points than compounds with straight chains.
Physical Properties of Alkyl Halides - Densities Alkyl fluorides are comparable to alkanes and are less dense than water. Alkyl chlorides with one Cl are less dense than water. Alkyl bromides and iodides are denser than water.
Preparation of Alkyl Halides - Allylic Bromination We will learn other ways to prepare alkyl halides in later units. Free-radical halogenations often give a mixture of products. Allylic bromination, a free-radical process, can be selective.
Allylic Bromination - Overall Reaction NBS, n-bromosuccinimide, is often used as the source of bromine. That way, the amount of bromine is kept low…why? H 2 C=CH-CH 2 -CH 3 H 2 C=CH-CHBr-CH 3 + H 2 CBr-CH=CH 2 -CH 3 NBS, hv
Allylic Bromination - NBS ++ Br 2 is present in trace amounts in NBS (for initiation), and HBr is formed as soon as any products are formed, and so is available to produce more Br 2.