organic chemistry

Cards (223)

  • What is a hydrocarbon?
    A compound consisting of hydrogen and carbon only
  • What does the molecular formula represent?
    The actual number of each type of atom in a compound
  • What characterizes an unsaturated compound?
    It contains a C=C double bond
  • What defines a saturated compound?
    It contains single carbon-carbon bonds only
  • What is a general formula in organic chemistry?
    An algebraic formula for a homologous series, e.g., CnH2n_nH_{2n}
  • What does the empirical formula represent?
    It shows the simplest whole number ratio of atoms of each element in the compound
  • What is a displayed formula?
    • Shows all the covalent bonds present in a molecule
    • Includes all atoms and their connections
  • How should hydrogen atoms be added when drawing organic compounds?
    So that each carbon has 4 bonds
  • What is the shape around the carbon atom in saturated hydrocarbons?
    The shape is tetrahedral with a bond angle of 109.5°
  • What is a skeletal formula?
    • A simplified organic formula
    • Shows the carbon skeleton and associated functional groups
    • Hydrogen atoms are removed from alkyl chains
  • What is a structural formula?
    • Shows the minimal detail of the arrangement of atoms in a molecule
    • Example for butane: CH3CH2CH2CH3_3CH_2CH_2CH_3 or CH3(CH2)2CH3_3(CH_2)_2CH_3
  • What are homologous series?
    • Families of organic compounds with the same functional group
    • Same general formula
    • Gradual change in physical properties (e.g., boiling point)
    • Each member differs by CH2_2 from the last
  • What is a functional group?
    An atom or group of atoms that causes different molecules to have similar chemical properties
  • What are the suffixes and prefixes for different functional groups?
    • Alkanes: -ane
    • Alkenes: -ene
    • Alcohols: -ol (hydroxy-)
    • Halogenoalkanes: chloro-, bromo-, iodo-
    • Aldehydes: -al (formyl-)
    • Ketones: -one (oxo-)
    • Carboxylic acids: -oic acid
    • Esters: -yl –oate
  • What is the general formula for alkanes?
    CnH2n+2_nH_{2n+2}
  • How do you name branched carbon chains?
    Count the longest carbon chain and name appropriately, then add prefixes for branched chains
  • How do you indicate the position of a functional group on a carbon chain?
    By using a number that gives the functional group the lowest number
  • What is the rule for separating words and numbers in naming compounds?
    Words are separated by dashes and numbers are separated by commas
  • What happens when a suffix starts with a vowel in naming compounds?
    You remove the -e from the stem alkane name
  • What is the priority order for functional groups in naming compounds?
    Carboxylic acids > aldehydes > ketones > alcohols > alkenes > halogenoalkanes
  • What are the basic rules for naming functional groups?
    • Use the appropriate suffix or prefix
    • Include position numbers if necessary
    • List groups in alphabetical order (ignoring di, tri)
  • What is the suffix for aldehydes?

    • al
  • What is the suffix for ketones?

    • one
  • What is the suffix for carboxylic acids?
    • oic acid
  • How do you name compounds with multiple functional groups?
    The highest precedence group takes the suffix, and others take the prefix form
  • What is structural isomerism?
    • Same molecular formula but different structures
    • Includes chain isomerism, position isomerism, and functional group isomerism
  • What is chain isomerism?
    Compounds with the same molecular formula but different structures of the carbon skeleton
  • What is position isomerism?
    Compounds with the same molecular formula but different positions of the same functional group
  • What is functional group isomerism?
    Compounds with the same molecular formula but different functional groups
  • What is stereoisomerism?
    • Same structural formulae but different spatial arrangement of atoms
    • Alkenes can exhibit E-Z stereoisomerism
  • What causes E-Z stereoisomerism?
    Restricted rotation about the C=C bond and different groups attached to the double bond
  • How do you label E-Z isomers?
    If the priority atom is on the same side, it is labeled Z; if on opposite sides, it is labeled E
  • What is the priority group in E-Z isomerism?
    The atom with the bigger atomic number is classed as the priority atom
  • How does but-1-ene differ from but-2-ene in terms of isomerism?
    But-1-ene is a structural isomer of but-2-ene but does not show E-Z isomerism
  • What is the significance of the C=O bond in aldehydes?
    It is always on the first carbon of the chain, so it does not need an extra number
  • How do you name ketones with 5 or more carbons?
    They need a number to show the position of the double bond
  • What is the naming convention for carboxylic acids?
    They end in -oic acid and do not require a number for the acid group
  • What is the name for a compound with two carboxylic acid groups?
    • dioic acid
  • How do you name compounds with two ketone groups?
    Use di before -one and add an e to the stem
  • How do you name compounds with two aldehyde groups?
    Use di before -al and add an e to the stem