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Carbon Chapter 4
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Carbon
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Organic chemistry Study of carbon compounds All life contains carbon
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Carbon 4 valence electrons 4 covalent bonds Single, double and triple bonds Oxygen, hydrogen and nitrogen
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Urea
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Hydrocarbons Molecules containing only carbon & hydrogen Chains Rings Branch
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Hydrocarbons
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Octane
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A fat molecule Hydrocarbons
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Isomers Compounds with the same molecular formula But different structures & properties Structural isomers: Different covalent arrangements of their atoms Geometric isomers: Same covalent arrangements but differ in spatial arrangements
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Isomers Enantiomers: Isomers that are mirror images of each other
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Fig. 4-7 Pentane (a) Structural isomers (b) Geometric isomers 2-methyl butane cis isomer: The two Xs are on the same side. trans isomer: The two Xs are on opposite sides. (c) Enantiomers L isomer D isomer
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Structural isomers
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(R)-ibuprofen (S)-ibuprofen Eantiomers
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Fig. 4-UN9 L -dopa D -dopa
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Fig. 4-8 Drug Ibuprofen Albuterol Condition Pain; inflammation Asthma Effective Enantiomer S-Ibuprofen R-Albuterol R-Ibuprofen S-Albuterol Ineffective Enantiomer
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Functional groups Chemical groups attached to a carbon Unique chemical properties
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Fig. 4-9 Estradiol Testosterone
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Functional groups 1. Hydroxyl -OH Alcohols 2. Carboxyl -COOH Organic acids
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Functional groups 3. Carbonyl C=O Aldehydes and ketones 4. Amino -NH 2 Amines
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Functional groups 5. Sulfhydryl -SH Thiols 6. Phosphates -OPO 3 -3 7. Methyl -CH 3
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Functional groups
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ATP Adenosine triphosphate
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