![Page 1: Chemistry 30 Organic Chemistry NOTES. 11. Reactivity of Alkanes, Alkenes and Alkynes Most to least – alkynes (4 bonding electrons available), alkenes](https://reader034.vdocuments.net/reader034/viewer/2022042503/56649e5f5503460f94b58bb3/html5/thumbnails/1.jpg)
Chemistry 30Chemistry 30
Organic Chemistry Organic Chemistry NOTESNOTES
![Page 2: Chemistry 30 Organic Chemistry NOTES. 11. Reactivity of Alkanes, Alkenes and Alkynes Most to least – alkynes (4 bonding electrons available), alkenes](https://reader034.vdocuments.net/reader034/viewer/2022042503/56649e5f5503460f94b58bb3/html5/thumbnails/2.jpg)
11. Reactivity of Alkanes, Alkenes and Alkynes
Most to least – alkynes (4 Most to least – alkynes (4 bonding electrons available), bonding electrons available), alkenes (2 bonding electrons), alkenes (2 bonding electrons), and alkanes (no bonding and alkanes (no bonding electrons). electrons).
![Page 3: Chemistry 30 Organic Chemistry NOTES. 11. Reactivity of Alkanes, Alkenes and Alkynes Most to least – alkynes (4 bonding electrons available), alkenes](https://reader034.vdocuments.net/reader034/viewer/2022042503/56649e5f5503460f94b58bb3/html5/thumbnails/3.jpg)
III. Important Uses of AliphaticsIII. Important Uses of Aliphatics
1. Alkanes – methane (natural gas), 1. Alkanes – methane (natural gas), butane (lighter fluid)butane (lighter fluid)
![Page 4: Chemistry 30 Organic Chemistry NOTES. 11. Reactivity of Alkanes, Alkenes and Alkynes Most to least – alkynes (4 bonding electrons available), alkenes](https://reader034.vdocuments.net/reader034/viewer/2022042503/56649e5f5503460f94b58bb3/html5/thumbnails/4.jpg)
2. Alkenes – ethene: used in making 2. Alkenes – ethene: used in making plasticplastic
![Page 5: Chemistry 30 Organic Chemistry NOTES. 11. Reactivity of Alkanes, Alkenes and Alkynes Most to least – alkynes (4 bonding electrons available), alkenes](https://reader034.vdocuments.net/reader034/viewer/2022042503/56649e5f5503460f94b58bb3/html5/thumbnails/5.jpg)
3. Alkynes – ethyne (acetylene): used in 3. Alkynes – ethyne (acetylene): used in welding welding
![Page 6: Chemistry 30 Organic Chemistry NOTES. 11. Reactivity of Alkanes, Alkenes and Alkynes Most to least – alkynes (4 bonding electrons available), alkenes](https://reader034.vdocuments.net/reader034/viewer/2022042503/56649e5f5503460f94b58bb3/html5/thumbnails/6.jpg)
IV. Aromatics IV. Aromatics
1.1. Definition:
A special class of A special class of cyclic unsaturatedcyclic unsaturated hydrocarbons is known as aromatic hydrocarbons is known as aromatic hydrocarbons. The simplest of these hydrocarbons. The simplest of these is is benzenebenzene (C (C66HH66).).
However, evidence indicates that the However, evidence indicates that the bonds between the C’s are equal in bonds between the C’s are equal in length and strength.length and strength.
![Page 7: Chemistry 30 Organic Chemistry NOTES. 11. Reactivity of Alkanes, Alkenes and Alkynes Most to least – alkynes (4 bonding electrons available), alkenes](https://reader034.vdocuments.net/reader034/viewer/2022042503/56649e5f5503460f94b58bb3/html5/thumbnails/7.jpg)
C
C
C
C
C
C
H
H
H
H
H
H
![Page 8: Chemistry 30 Organic Chemistry NOTES. 11. Reactivity of Alkanes, Alkenes and Alkynes Most to least – alkynes (4 bonding electrons available), alkenes](https://reader034.vdocuments.net/reader034/viewer/2022042503/56649e5f5503460f94b58bb3/html5/thumbnails/8.jpg)
So, the actual structure is a mixture of: So, the actual structure is a mixture of:
+
![Page 9: Chemistry 30 Organic Chemistry NOTES. 11. Reactivity of Alkanes, Alkenes and Alkynes Most to least – alkynes (4 bonding electrons available), alkenes](https://reader034.vdocuments.net/reader034/viewer/2022042503/56649e5f5503460f94b58bb3/html5/thumbnails/9.jpg)
Therefore, benzene is represented by:
![Page 10: Chemistry 30 Organic Chemistry NOTES. 11. Reactivity of Alkanes, Alkenes and Alkynes Most to least – alkynes (4 bonding electrons available), alkenes](https://reader034.vdocuments.net/reader034/viewer/2022042503/56649e5f5503460f94b58bb3/html5/thumbnails/10.jpg)
22.. Nomenclature of Alkyl-Benzene Compounds Nomenclature of Alkyl-Benzene Compounds
USE THE FOLLOWING STEPS:USE THE FOLLOWING STEPS:
a) name the alkyl group followed by benzene
Example: methylbenzene Example: methylbenzene
(toluene)(toluene)
CH3
![Page 11: Chemistry 30 Organic Chemistry NOTES. 11. Reactivity of Alkanes, Alkenes and Alkynes Most to least – alkynes (4 bonding electrons available), alkenes](https://reader034.vdocuments.net/reader034/viewer/2022042503/56649e5f5503460f94b58bb3/html5/thumbnails/11.jpg)
b) if the alkyl group is attached by a middle carbon, consider, the benzene as an alkyl group called phenylphenyl
Example: 2-phenylpropane Example: 2-phenylpropane CH CH3CH3
![Page 12: Chemistry 30 Organic Chemistry NOTES. 11. Reactivity of Alkanes, Alkenes and Alkynes Most to least – alkynes (4 bonding electrons available), alkenes](https://reader034.vdocuments.net/reader034/viewer/2022042503/56649e5f5503460f94b58bb3/html5/thumbnails/12.jpg)
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) CH3
CH2 CH3
CH3
CH2 CH3
CH3
CH2 CH3 O-ethylmethylbenzene
or
1-ethyl-2-methylbenzene
M-ethylmethylbenzene
or
1-ethyl-3-methylbenzene
P-ethylmethylbenzene
or
1-ethyl-4-methylbenzene
![Page 13: Chemistry 30 Organic Chemistry NOTES. 11. Reactivity of Alkanes, Alkenes and Alkynes Most to least – alkynes (4 bonding electrons available), alkenes](https://reader034.vdocuments.net/reader034/viewer/2022042503/56649e5f5503460f94b58bb3/html5/thumbnails/13.jpg)
d) if 3 H’s are replaced, number so that the lowest possible number combination is achieved. Then name alphabetically.
![Page 14: Chemistry 30 Organic Chemistry NOTES. 11. Reactivity of Alkanes, Alkenes and Alkynes Most to least – alkynes (4 bonding electrons available), alkenes](https://reader034.vdocuments.net/reader034/viewer/2022042503/56649e5f5503460f94b58bb3/html5/thumbnails/14.jpg)
Example:
i. 1-ethyl-3-methyl-5-propylbenzene
NOT 3-ethyl-5-methyl-1-propylbenzene
CH3
CH2 CH3CH2CH2CH3
![Page 15: Chemistry 30 Organic Chemistry NOTES. 11. Reactivity of Alkanes, Alkenes and Alkynes Most to least – alkynes (4 bonding electrons available), alkenes](https://reader034.vdocuments.net/reader034/viewer/2022042503/56649e5f5503460f94b58bb3/html5/thumbnails/15.jpg)
ii. 4-ethyl-1,2-dimethylbenzene
NOT 1-ethyl-3,4-dimethylbenzene
CH3
CH3CH2
CH3
![Page 16: Chemistry 30 Organic Chemistry NOTES. 11. Reactivity of Alkanes, Alkenes and Alkynes Most to least – alkynes (4 bonding electrons available), alkenes](https://reader034.vdocuments.net/reader034/viewer/2022042503/56649e5f5503460f94b58bb3/html5/thumbnails/16.jpg)
3. Properties of Benzene3. 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
![Page 17: Chemistry 30 Organic Chemistry NOTES. 11. Reactivity of Alkanes, Alkenes and Alkynes Most to least – alkynes (4 bonding electrons available), alkenes](https://reader034.vdocuments.net/reader034/viewer/2022042503/56649e5f5503460f94b58bb3/html5/thumbnails/17.jpg)
Example:
+ Cl Cl
Cl
+ ClH
This is because there is no definite double bond for the addition reaction to occur on.
![Page 18: Chemistry 30 Organic Chemistry NOTES. 11. Reactivity of Alkanes, Alkenes and Alkynes Most to least – alkynes (4 bonding electrons available), alkenes](https://reader034.vdocuments.net/reader034/viewer/2022042503/56649e5f5503460f94b58bb3/html5/thumbnails/18.jpg)
3. Properties of Benzene3. Properties of Benzene
Also found in number of explosives
Example: trinitrotoluene (TNT)
CH3
N+
O-
O
N+
O-
O
N+
O-
O
![Page 19: Chemistry 30 Organic Chemistry NOTES. 11. Reactivity of Alkanes, Alkenes and Alkynes Most to least – alkynes (4 bonding electrons available), alkenes](https://reader034.vdocuments.net/reader034/viewer/2022042503/56649e5f5503460f94b58bb3/html5/thumbnails/19.jpg)
A little more about Benzene
benzin, benzol, benzene
![Page 20: Chemistry 30 Organic Chemistry NOTES. 11. Reactivity of Alkanes, Alkenes and Alkynes Most to least – alkynes (4 bonding electrons available), alkenes](https://reader034.vdocuments.net/reader034/viewer/2022042503/56649e5f5503460f94b58bb3/html5/thumbnails/20.jpg)
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
![Page 21: Chemistry 30 Organic Chemistry NOTES. 11. Reactivity of Alkanes, Alkenes and Alkynes Most to least – alkynes (4 bonding electrons available), alkenes](https://reader034.vdocuments.net/reader034/viewer/2022042503/56649e5f5503460f94b58bb3/html5/thumbnails/21.jpg)
![Page 22: Chemistry 30 Organic Chemistry NOTES. 11. Reactivity of Alkanes, Alkenes and Alkynes Most to least – alkynes (4 bonding electrons available), alkenes](https://reader034.vdocuments.net/reader034/viewer/2022042503/56649e5f5503460f94b58bb3/html5/thumbnails/22.jpg)
![Page 23: Chemistry 30 Organic Chemistry NOTES. 11. Reactivity of Alkanes, Alkenes and Alkynes Most to least – alkynes (4 bonding electrons available), alkenes](https://reader034.vdocuments.net/reader034/viewer/2022042503/56649e5f5503460f94b58bb3/html5/thumbnails/23.jpg)
![Page 24: Chemistry 30 Organic Chemistry NOTES. 11. Reactivity of Alkanes, Alkenes and Alkynes Most to least – alkynes (4 bonding electrons available), alkenes](https://reader034.vdocuments.net/reader034/viewer/2022042503/56649e5f5503460f94b58bb3/html5/thumbnails/24.jpg)
Uses
After-shave lotion Solvent for degreasing metals Decaffeinate coffee paint strippers rubber cements spot removers gasoline additive
![Page 25: Chemistry 30 Organic Chemistry NOTES. 11. Reactivity of Alkanes, Alkenes and Alkynes Most to least – alkynes (4 bonding electrons available), alkenes](https://reader034.vdocuments.net/reader034/viewer/2022042503/56649e5f5503460f94b58bb3/html5/thumbnails/25.jpg)
![Page 26: Chemistry 30 Organic Chemistry NOTES. 11. Reactivity of Alkanes, Alkenes and Alkynes Most to least – alkynes (4 bonding electrons available), alkenes](https://reader034.vdocuments.net/reader034/viewer/2022042503/56649e5f5503460f94b58bb3/html5/thumbnails/26.jpg)
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”
![Page 27: Chemistry 30 Organic Chemistry NOTES. 11. Reactivity of Alkanes, Alkenes and Alkynes Most to least – alkynes (4 bonding electrons available), alkenes](https://reader034.vdocuments.net/reader034/viewer/2022042503/56649e5f5503460f94b58bb3/html5/thumbnails/27.jpg)
Still used today...
Max 1% as a gasoline additive to make styrene and Nylon rubbers lubricants dyes detergents drugs explosives & napalm pesticides
![Page 28: Chemistry 30 Organic Chemistry NOTES. 11. Reactivity of Alkanes, Alkenes and Alkynes Most to least – alkynes (4 bonding electrons available), alkenes](https://reader034.vdocuments.net/reader034/viewer/2022042503/56649e5f5503460f94b58bb3/html5/thumbnails/28.jpg)
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!