Aside from the multiple ring systems shown in the table, Naphthalene, Anthracene,Phenanthrene Chrysene,Pyrene, and Benzopyrene. Search for 1 multiple ring aromatic compound and list down its properties, sources, and uses or applications.
Aside from the multiple ring systems shown in the table, Naphthalene, Anthracene,Phenanthrene Chrysene,Pyrene, and Benzopyrene. Search for 1 multiple ring aromatic compound and list down its properties, sources, and uses or applications.
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Question
Aside from the multiple ring systems shown in the table, Naphthalene, Anthracene,Phenanthrene Chrysene,Pyrene, and Benzopyrene. Search for 1
multiple ring aromatic compound and list down its properties, sources, and uses or
applications.
Transcribed Image Text:Name and Structure
Properties
Uses
MULTIPLE RING SYSTEMS
White volatile crystals with
coal tar aroma
Moth repellants
Fungicides
Lubricants
Naphthalene
r.d. = 1.162 g/ml
m.p. = 80.1°C
b.p.= 218°C
Resins
Solvent
Colorless, crystalline
substance with violet
fluorescence
Source of dye
Coating
applications
Anthracene
r.d. = 1.25g/ml
m.p. = 218°C
b.p.= 342°C
Colorless, crystalline
hydrocarbon
r.d. = 1.179 g/ml
m.p. = 100°C
b.p.= 340°C
Synthesis of dyes
and drugs
Phenanthrene
2 | Page
Polynuclear hydrocarbon
which gives a bluish
fluorescence
Chrysene
Organic synthesis
r.d. = 1.274 g/ml
m.p. = 254°C
b.p.= 488°C
Pyrene
Colorless solid with blue
Organic synthesis
fluorescence derived from
alcohol or by sublimation
r.d. = 1.271 g/ml
m.p. = 156°C
b.p.= 404°C
One of the most potent
carcinogenic material
found in tobacco smoke
Benzopyrene
Organic synthesis
r.d. = 1.351g/ml
m.p. = 178°C
b.p.= 495°C
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