4- organic compounds

Cards (58)

  • What is a hydrocarbon?
    A compound of carbon and hydrogen only
  • What determines the principal characteristic properties of a molecule?
    The functional group in the molecule
  • What type of bonds does a saturated compound contain?
    C to C single bonds
  • What type of bonds does an unsaturated compound contain?
    C to C multiple bonds
  • What is the process to find the longest carbon chain in a compound?
    1. Identify and number the longest C chain.
    2. Determine the code for the compound's name.
  • What does the term "organic compounds" historically refer to?
    Compounds derived from living species
  • Why is it important to know the homologous series when naming organic compounds?
    It helps identify the functional group present
  • What are the homologous series mentioned in the study material?
    • Alkanes: saturated hydrocarbons
    • Alkenes: unsaturated hydrocarbons with C=C double bond
    • Haloalkanes: hydrogen replaced by halogen
    • Primary (1°) alcohols: contain -OH group
    • Carboxylic acids: contain -COOH group
  • What is the code for one carbon in organic compound naming?
    meth
  • What is the code for five carbons in organic compound naming?
    pent
  • What is the code for nine carbons in organic compound naming?
    non
  • What is the code for two carbons in organic compound naming?
    eth
  • What is the code for six carbons in organic compound naming?
    hex
  • What is the code for ten carbons in organic compound naming?
    dec
  • What is the code for three carbons in organic compound naming?
    prop
  • What is the code for seven carbons in organic compound naming?
    hept
  • What is the code for four carbons in organic compound naming?
    but
  • What is the code for eight carbons in organic compound naming?
    oct
  • What are the rules for naming organic compounds?
    1. Find the longest continuous carbon chain.
    2. Number the C atoms for smallest substituent numbers.
    3. Use prefixes (di, tri, tetra) for multiple side chains.
    4. Maintain alphabetical order of branch names.
  • What is the name of the -CH₃ group?
    Methyl
  • What does the displayed formula show?
    All the bonds in the molecule
  • What does the molecular formula display?
    Total number of atoms of each element
  • What is a skeletal formula?
    A simplified representation of the molecule
  • What is a homologue in organic chemistry?
    A series differing by a CH₂ group
  • What are the characteristics of a homologous series?
    1. General formula representation.
    2. Differ by a CH₂ unit.
    3. Similar chemical properties.
    4. Gradual change in physical properties with molecular mass.
  • What is the empirical formula based on?
    The ratio of atoms in a compound
  • How do you calculate the empirical formula from masses?
    Use mass ratios of elements
  • What is the empirical formula for a hydrocarbon with 0.205 g burned producing 0.600 g CO₂ and 0.225 g H₂O?
    CH₂
  • How do you find the molecular formula from the empirical formula?
    Use the molar mass ratio
  • What is the molecular formula if the empirical formula is CH₂ and Mr is approximately 80?
    C₆H₁₂
  • What is the empirical formula for a compound with C = 60.0%, H = 13.3%, O = 26.7%?

    C₅H₂O
  • What is the molecular formula if the empirical formula is C₅H₂O and Mr is 60?
    C₅H₁₀O
  • What are the types of structural isomerism?
    1. Chain isomerism
    2. Position isomerism
    3. Functional group isomerism
  • What is chain isomerism?
    Different arrangements of the carbon chain
  • What is position isomerism?
    Functional group in different positions
  • What is functional group isomerism?
    Different functional groups present
  • What is E-Z isomerism?
    • Consists of cis and trans isomers.
    • Rotation about the double bond is restricted.
  • What is the significance of E-Z isomerism?
    It affects physical and chemical properties
  • How do you determine E-Z isomers?
    By comparing atoms attached to double bond carbons
  • What happens to the physical properties of E-Z isomers?
    They can differ due to functional group arrangement