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Chemistry 30 Organic Chemistry NOTES. 11. Reactivity of Alkanes, Alkenes and Alkynes  Most to least – alkynes (4 bonding electrons available), alkenes.

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Presentation on theme: "Chemistry 30 Organic Chemistry NOTES. 11. Reactivity of Alkanes, Alkenes and Alkynes  Most to least – alkynes (4 bonding electrons available), alkenes."— Presentation transcript:

1 Chemistry 30 Organic Chemistry NOTES

2 11. Reactivity of Alkanes, Alkenes and Alkynes  Most to least – alkynes (4 bonding electrons available), alkenes (2 bonding electrons), and alkanes (no bonding electrons).

3 III. Important Uses of Aliphatics 1. Alkanes – methane (natural gas), butane (lighter fluid) 1. Alkanes – methane (natural gas), butane (lighter fluid)

4 2. Alkenes – ethene: used in making plastic

5 3. Alkynes – ethyne (acetylene): used in welding

6 IV. Aromatics 1. 1. Definition: A special class of cyclic unsaturated hydrocarbons is known as aromatic hydrocarbons. The simplest of these is benzene (C 6 H 6 ). However, evidence indicates that the bonds between the C’s are equal in length and strength.

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8 So, the actual structure is a mixture of:

9 Therefore, benzene is represented by:

10 2. Nomenclature of Alkyl-Benzene Compounds USE THE FOLLOWING STEPS: a) name the alkyl group followed by benzene Example: methylbenzene (toluene) (toluene)

11 phenyl b) if the alkyl group is attached by a middle carbon, consider, the benzene as an alkyl group called phenyl Example: 2-phenylpropane

12 c) if 2 H’s are replaced in benzene, the replaced groups can be arranged in 3 ways Example: 1. Ortho 2. Meta 3. Para (adjacent C’s) (1C between) (2C’s between ) O-ethylmethylbenzene or 1-ethyl-2-methylbenzene M-ethylmethylbenzene or 1-ethyl-3-methylbenzene P-ethylmethylbenzene or 1-ethyl-4-methylbenzene

13 d) if 3 H’s are replaced, number so that the lowest possible number combination is achieved. Then name alphabetically.

14 Example: i. 1-ethyl-3-methyl-5-propylbenzene NOT 3-ethyl-5-methyl-1-propylbenzene

15 ii. 4-ethyl-1,2-dimethylbenzene NOT 1-ethyl-3,4-dimethylbenzene

16 3. Properties of Benzene Liquid at room temperature, boils at 80.1 C Non-polar so insoluble in water Behaves like an alkane: addition reaction do NOT occur Substitution reactions DO occur

17 Example: This is because there is no definite double bond for the addition reaction to occur on.

18 3. Properties of Benzene Also found in number of explosives Example: trinitrotoluene (TNT)

19 A little more about Benzene benzin, benzol, benzene

20 Discovery 1825- Michael Faraday- first to isolate & identify 1836- Auguste Laurent (French) named it “phène” 1855- August Wilhelm Hofmann used the word “aromatic” to describe the family. 1865- Friedrich August Kekulé (German) had a dream

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24 Uses After-shave lotion Solvent for degreasing metals Decaffeinate coffee paint strippers rubber cements spot removers gasoline additive

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26 Health Issues... “it’s generally considered that the only absolutly safe concentration for benzene is zero” (The American Petroleum Institute, 1948) Know carcinogen- causes leukemia Was first known to cause cancer in the 1920s but it wasn’t until 1979 until it was “conclusive”

27 Still used today... Max 1% as a gasoline additive to make styrene and Nylon rubbers lubricants dyes detergents drugs explosives & napalm pesticides

28 Learning Activities Groups of 2: Make six flash cards. Draw a diagram on one side, name it on the other! Don’t forget IUPAC! Homework Page 11 Go back through the workbook and find any aromatic question that we skipped!


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