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1 Organic Chemistry, Second Edition Janice Gorzynski Smith University of Hawai’i Chapter 8 Alkyl Halides and Elimination Reactions Copyright © The McGraw-Hill.

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Presentation on theme: "1 Organic Chemistry, Second Edition Janice Gorzynski Smith University of Hawai’i Chapter 8 Alkyl Halides and Elimination Reactions Copyright © The McGraw-Hill."— Presentation transcript:

1 1 Organic Chemistry, Second Edition Janice Gorzynski Smith University of Hawai’i Chapter 8 Alkyl Halides and Elimination Reactions Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Prepared by Rabi Ann Musah State University of New York at Albany

2 2 Elimination reactions involve the loss of elements from the starting material to form a new  bond in the product. General Features of Elimination

3 3 Equations [1] and [2] illustrate examples of elimination reactions. In both reactions a base removes the elements of an acid, HX, from the organic starting material. General Features of Elimination

4 4 Removal of the elements HX is called dehydrohalogenation. Dehydrohalogenation is an example of  elimination. The curved arrow formalism shown below illustrates how four bonds are broken or formed in the process. General Features of Elimination

5 5 The most common bases used in elimination reactions are negatively charged oxygen compounds, such as HO ¯ and its alkyl derivatives, RO ¯, called alkoxides. General Features of Elimination

6 6 To draw any product of dehydrohalogenation—Find the  carbon. Identify all  carbons with H atoms. Remove the elements of H and X from the  and  carbons and form a  bond. General Features of Elimination

7 7 Recall that the double bond of an alkene consists of a  bond and a  bond. Alkenes—The Products of Elimination

8 8 Alkenes are classified according to the number of carbon atoms bonded to the carbons of the double bond. Figure 8.1 Classifying alkenes by the number of R groups bonded to the double bond Alkenes—The Products of Elimination

9 9 Recall that rotation about double bonds is restricted. Alkenes—The Products of Elimination

10 10 Because of restricted rotation, two stereoisomers of 2- butene are possible. cis-2-Butene and trans-2-butene are diastereomers, because they are stereoisomers that are not mirror images of each other. Alkenes—The Products of Elimination

11 11 Whenever the two groups on each end of a carbon- carbon double bond are different from each other, two diastereomers are possible. Alkenes—The Products of Elimination

12 12 In general, trans alkenes are more stable than cis alkenes because the groups bonded to the double bond carbons are further apart, reducing steric interactions. Alkenes—The Products of Elimination

13 13 The stability of an alkene increases as the number of R groups bonded to the double bond carbons increases. The higher the percent s-character, the more readily an atom accepts electron density. Thus, sp 2 carbons are more able to accept electron density and sp 3 carbons are more able to donate electron density. Consequently, increasing the number of electron donating groups on a carbon atom able to accept electron density makes the alkene more stable. Alkenes—The Products of Elimination

14 14 trans-2-Butene (a disubstituted alkene) is more stable than cis-2-butene (another disubstituted alkene), but both are more stable than 1-butene (a monosubstituted alkene). Alkenes—The Products of Elimination

15 15 There are two mechanisms of elimination—E2 and E1, just as there are two mechanisms of substitution, S N 2 and S N 1. E2 mechanism—bimolecular elimination E1 mechanism—unimolecular elimination The E2 and E1 mechanisms differ in the timing of bond cleavage and bond formation, analogous to the S N 2 and S N 1 mechanisms. E2 and S N 2 reactions have some features in common, as do E1 and S N 1 reactions. Mechanisms of Elimination

16 16 The most common mechanism for dehydrohalogenation is the E2 mechanism. It exhibits second-order kinetics, and both the alkyl halide and the base appear in the rate equation, i.e., Mechanisms of Elimination—E2 rate = k[(CH 3 ) 3 CBr][ ¯ OH] The reaction is concerted—all bonds are broken and formed in a single step.

17 17 Mechanisms of Elimination—E2

18 18 Figure 8.4 An E2 elimination with DBN used as the base Mechanisms of Elimination—E2

19 19 Mechanisms of Elimination—E2

20 20 Mechanisms of Elimination—E2

21 21 Mechanisms of Elimination—E2 Figure 8.5 Two examples of the E2 reaction used in organic synthesis

22 22 Recall that when alkyl halides have two or more different  carbons, more than one alkene product is formed. When this happens, one of the products usually predominates. The major product is the more stable product—the one with the more substituted double bond. This phenomenon is called the Zaitsev rule. The Zaitsev (Saytzeff) Rule

23 23 The Zaitsev rule: the major product in  elimination has the more substituted double bond. A reaction is regioselective when it yields predominantly or exclusively one constitutional isomer when more than one is possible. Thus, the E2 reaction is regioselective.

24 24 When a mixture of stereoisomers is possible from a dehydrohalogenation, the major product is the more stable stereoisomer. A reaction is stereoselective when it forms predominantly or exclusively one stereoisomer when two or more are possible. The E2 reaction is stereoselective because one stereoisomer is formed preferentially. The Zaitsev (Saytzeff) Rule


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