Textbook

Cards (46)

  • Organic Chemistry
    The study of carbon-based compounds
  • Organic chemists
    • Synthetic organic chemists
    • Bioorganic chemists
    • Natural products chemists
    • Physical organic chemists
    • Organometallic chemists
    • Computational chemists
    • Materials chemists
  • Electron configuration
    The arrangement of electrons in an atom's orbitals
  • Ionic bonding
    Bonding that occurs when atoms transfer electrons from one to another
  • Covalent bonding
    Bonding that occurs when atoms share electrons
  • Dipole moment
    The separation of charge within a molecule
  • Hybrid orbitals
    Orbitals formed by the mixing of atomic orbitals
  • Sigma and pi bonding
    Types of covalent bonding
  • Lewis structures
    Diagrams that show the arrangement of atoms and their bonding in a molecule
  • Drawing resonance structures
    1. Identify resonance contributors
    2. Draw resonance structures following rules
    3. Assign importance to resonance structures
  • Acid-base definitions

    • Arrhenius acids and bases
    • Brønsted-Lowry acids and bases
    • Lewis acids and bases
  • pKa
    A quantitative scale of acidity
  • Functional groups
    • Alkanes
    • Alkenes
    • Alkynes
    • Aromatics
    • Halides
    • Alcohols
    • Thiols
    • Ethers
    • Aldehydes
    • Ketones
    • Carboxylic acids
    • Esters
    • Amides
    • Amines
    • Nitriles
  • Organic Chemistry I Workbook For Dummies® is a book to help students learn organic chemistry
  • Thiols
    What stinks?
  • Aldehydes
    Living on the edge
  • Ketones
    Stuck in the middle
  • Esters
    Sweet-smelling compounds
  • Amides
    I am what I amide
  • Amines
    Be nice, don't be amine person
  • Test Your Knowledge
  • Stereochemistry
    Seeing in 3-D
  • Drawing Molecules in 3-D
    • Comparing Stereoisomers and Constitutional Isomers
  • Enantiomers
    Mirror Image Molecules
  • Chiral Centers
    Seeing Chiral Centers
  • Assigning Configurations to Chiral Centers
    1. Prioritizing the substituents
    2. Putting the number-four substituent in the back
    3. Drawing the curve
  • Meso Compounds

    The Consequences of Symmetry
  • Plane-Polarized Light

    Rotating Plane-Polarized Light
  • Diastereomers
    Multiple Chiral Centers
  • Representing 3-D Structures on Paper
    Fischer Projections
  • Rules for using Fischer projections
  • Seeing stereoisomerism with Fischer projections
  • Spotting meso compounds with Fischer projections
  • Keeping the Jargon Straight
  • Alkanes
    What's in a Name?
  • Straight-Chain Alkanes
    • Reaching Out: Branching Alkanes
  • Drawing Alkanes
    Converting a Name to a Structure
  • Conformation of Straight-Chain Alkanes
    • Newman! Conformational analysis and Newman projections
    • Conformations of butane
  • Cycloalkanes
    • The stereochemistry of cycloalkanes
    • Conformations of cyclohexane
  • Reacting Alkanes: Free-Radical Halogenation
    1. Getting things started: Initiation
    2. Keeping the reaction going: Propagation
    3. You're fired: Termination steps