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Isomers Structural Isomers CH3 1. a) CH3 CH2 CH2 CH3 Butane (C4H10) CH3 CH CH3 2-methylpropane (C4H10) 2. CH2 CH CH2 CH3 1-butene CH3 CH2 C CH3 2-methylpropene CH3 CH CH CH3 CH2 CH2 2-butene CH2 CH2 CH CH2 CH2 CH3 cyclobutane methylcyclopropane 3. a) C4H8 has more isomers because the position of the double affects the name and because ring structures can be drawn. 4. aldehyde ketone ether H H H C C H H O C H H H O H C C C H H H H H C C H CH3 H O H H H OH C C C H H H H OH H C C C H O H alcohols H C H C C H H H C H H C H OH C H H 5. The OH bond is polar, the CO bond is less polar, thus the alcohol would have the higher boiling point and be soluble in water. 6. b) 1,2-dichloroethene requires cis or trans. 1,2-dichloroethane does not require cis or trans because they would both represent the same molecule (to move chlorine from the same side to opposite sides only requires that the C – C single bond be rotated). 7. CH CH3 3 CH3 cis-1,2-dimethylcyclopentane CH3 trans-1,2-dimethylcyclopentane CH3 CH3 8. 1,1-dimethylcyclopentane 9. a) not isomers (they don’t have the same chemical formula: C5H12 vs. C5H10) b) structural isomers c) geometric isomers d) not isomers (both diagrams represent the exact same molecule) Polymers 11. Monomer: the smallest repeating unit of a polymer (propene in polypropylene). Polymer: a long chain molecule made up of many small identical units (monomers). Addition polymerization: a reaction in which unsaturated monomers combine with each other to form a polymer. 12. Teflon, polypropylene, polyester, polyethylene (pop bottles, grocery bags), polystyrene (packing material), Plexiglas, polyvinyl chloride (vinyl), natural rubber, etc.