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22.2: Physical Properties of Arenes

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    The pleasant odors of the derivatives of many arenes is the origin of the name aromatic hydrocarbons. The arenes themselves generally are quite toxic; some are carcinogenic and inhalation of their vapors should be avoided. The volatile arenes are highly flammable and burn with a luminous sooty flame, in contrast to alkanes and alkenes, which usually burn with a bluish flame leaving little carbon residue.

    The more common arenes and their physical properties are given in Table 22-1. They are less dense than water and are highly insoluble. Boiling points increase regularly with increasing molecular weight, but there is little correlation between melting point and molecular weight. The melting point is highly dependent on the symmetry of the compound; thus benzene melts \(100^\text{o}\) higher than methylbenzene, and the more symmetrical 1,4-dimethylbenzene (para-xylene) has a higher boiling point than either the 1,2- or the 1,3-isomer. This latter fact is utilized in the separation by fractional crystallization of 1,4-dimethylbenzene from mixtures of isomers produced from petroleum.

    Table 22-1: Physical Properties of Arenes

    Roberts and Caserio Screenshot 22-2-1.png

    Contributors and Attributions

    John D. Robert and Marjorie C. Caserio (1977) Basic Principles of Organic Chemistry, second edition. W. A. Benjamin, Inc. , Menlo Park, CA. ISBN 0-8053-8329-8. This content is copyrighted under the following conditions, "You are granted permission for individual, educational, research and non-commercial reproduction, distribution, display and performance of this work in any format."

    This page titled 22.2: Physical Properties of Arenes is shared under a CC BY-NC-SA 4.0 license and was authored, remixed, and/or curated by John D. Roberts and Marjorie C. Caserio.