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Published byBritton Walters Modified over 9 years ago
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AROMATICS
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Complex carbon compounds that contain cyclical structures similar to and including benzene
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Aromatics compounds play a key role in biochemistry of living things: The 4 amino acids: histidine, phenylalanine, tryptophan and tyrosine build proteins All 5 nucleotides: adenine, thymine, cytosine, guanine and uracil make up the genetic code contain aromatics
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Benzene (C 6 H 6 ) simplest primary aromatic no true single or double bonds Electrons travel around a 6 carbon ring, causing the bonds to flip flop
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Phenyl Group Benzene loses a hydrogen atom and uses that bond to join other molecular structures
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Furan (C 4 H 4 O)
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Toluene (C 7 H 8 ) Aka Methyl Benzene
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Properties of Aromatics Extremely stable compounds that remain in the environment as Persistent Organic Pollutants Fragrant properties Non polar therefore non soluble in water
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Use of Aromatics phenyl groups are used in pharmaceuticals such as morphine, birth control pills, aspirin toluene is associated with TNT (2,4,6-trinitrotoluene)
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flavorful foods like chocolate, vanilla and cinnamon hormones Fibre polymers
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IUPAC Naming when benzene is the parent chain it is very similar to alkane naming number branches starting at the longest chain
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Benzene becomes a phenyl group when benzene is not attached to an end carbon or… when there is a double or triple bonds in another chain
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Example 3-methyl 1-propyl benzene 1-methyl furan
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Example 2
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Example 3
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