Chapter 12: Focus on Organic Chemistry: Unsaturated and Aromatic Hydrocarbons
Distinguish between organic and inorganic molecules
Name simple and branched alkanes
Classify organic molecules by functional groups
Predict polarity based on structure/formula
Compare physical properties (solubility, melting & boiling points) based on structure & functional groups
Write balanced combustion reactions for alkanes
Draw structures of organic molecules from names/formulas including isomers
Recognize chemical reactions in various organic functional groups
Identify organic reaction types from equations
Predict products of organic reactions from reactants
Saturated Hydrocarbons: Only single (C-C) bonds; maximum hydrogen atoms
Unsaturated Hydrocarbons: At least one C=C double bond or C≡C triple bond
Contain at least one C=C double bond
Can be linear, cyclic, or branched
Exhibit cis- and trans- stereoisomers due to rigid double bonds
Cis Isomer: Substituents on the same side of the double bond
Trans Isomer: Substituents on opposite sides
Differences in melting and boiling points due to spatial arrangement.
Cannot form cis-trans isomers if double bond carbons have identical groups
Example of molecules that do not exhibit isomerism
The role of retinal in vision, transitioning between 11-cis-retinal and all-trans-retinal
Drawing isomers and analyzing structural formulas
Contain at least one C≡C triple bond
Exhibit similar structural diversity (linear, cyclic, branched)
Reactive due to the ease of breaking double/triple bonds
Addition reactions lead to saturation by turning double/triple bonds into single bonds
Hydrogenation: Adds hydrogen, converting unsaturated to saturated
Adding water to alkenes results in a change from C=C to C-C, affecting product structures
A class of unsaturated hydrocarbons with rings of C atoms
Exhibit resonance: alternating C-C single and C=C double bonds
Example: Benzene (C6H6)
Common compounds: Vanillin, Ibuprofen, Aspirin, Acetaminophen
Identifying molecular types: alkane, alkene, alkyne, or aromatic
Review solutions for cis and trans isomer drawings, structural formula errors in reactions, and molecular classification.