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Chapter 4-Concept 4.2: Organic Chemical is study of CarbonVitalism idea that organic compounds arise only in organisms, was disprove when chemist synthesized those compoundsMechanism is the view that physical and chemical laws govern all natural phenomena. Experiments in organic chemistry caused shift from Vitalism to mechanism.1828 fredrich Wohler synthesized Urea from ammonium and cyante ions and cynate ions Herman Kolbe synthesized acetic acid from inorganic substances derived form elements.Stanly Miller’s classic experiment demonstrated the abiotic synthesis of organic compounds. Experiments support the idea that abiotic synthesis of organic compounds, perhaps near volcanoes, could have been a stage in the origin of life.-Concept 4.2: Carbon atoms can form diverse molecules by bonding to four other atomsCO2 O=C=OIs it organic? No because it does not have a hydrogen.-Molecular diversity arises from carbon skeleton skeleton Carbon chains form the skeleton of most organic molecules.-HydrocarbonsOnly carbon and hydrogenCan undergo reactions that release a lot of energyHydrocarbons are a major component of petroleum.-IsomersIsomers are compounds that have similar formulas but different structures.Structural Isomers: Different covalent arrangements (Branching our vs. not branching out)Cis-trans isomers: Same covalent bonds but differ in spatial arrangements.Enantiomers: Mirror image.-EnantiomersThese are important because one form can be helpful vs. being dangerous.Variations show how sensitive organisms are to subtle variations in molecules.-Thalidomide1950’s-60’s to cure morning sickness.Mixture of two enantiomersOne cured morning sicknessThe other caused birth defects.Used to cure Myeloma (Non-Pregnant women)-Concept 4.3: Chemical GroupsDistinctive properties of organic molecules depend on the carbon skeleton and on the molecular components attached to it.Functional groups: Components of organic molecules that are most commonly involved in chemical reactions.-7 Functional GroupsHydroxyl GroupForm hydrogen bonds with water to dissolve organic compoundsCarbonyl Group:Sugar, Aldose, KetoseAldehyde (Outside of molecule)Ketone (Inside of molecule)Carboxyl Group: Acts as an Acid gives away H+C-C-C=O(Acidic) -OHIf buffered at pH 7 (acts as an acid)C-C-C=O -O-Ester Group (Formed from Carboxylic Acid)C-C-C=O-O-RAmino Groups (Acts as a base, can pick up H+)C-NH2(Basic)C-NH3+(If buffered, Acidic)Sulfhydryl GroupC-S-H (Covalent bonds with another to stabilize proteins)Phosphate Group (Potential to react with water, release energy) (Acidic) (if buffered, acts as an acid)Methyl Group (Add to DNA, after its gene expression, arrangement of methyl groups is male and female sex hormones effects their shape and


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FSU BSC 2010 - Chapter 4

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