Alcohols

Cards (72)

  • What is the general formula for alcohols?
    C<sub>n</sub>H<sub>2n+1</sub>OH
  • How are alcohols named?
    They end in -ol with position numbers
  • What is the name of the compound with the structure CH<sub>3</sub>CH(OH)CH<sub>2</sub>CH<sub>3</sub>?
    butan-2-ol
  • What prefix is used for an -OH group when other functional groups are present?
    hydroxy-
  • What is the name of the compound CH<sub>3</sub>CH(OH)COOH?
    1. hydroxypropanoic acid
  • How are multiple -OH groups indicated in alcohol naming?
    Using di, tri, etc., with an 'e'
  • What is the name of the compound with the formula C<sub>2</sub>H<sub>6</sub>O and two -OH groups?
    ethane-1,2-diol
  • What defines a primary alcohol?
    One carbon attached to the carbon with -OH
  • What defines a secondary alcohol?
    Two carbons attached to the carbon with -OH
  • What defines a tertiary alcohol?
    Three carbons attached to the carbon with -OH
  • What is the bond angle for H-C-H and C-C-O in alcohols?
    109.5°
  • What is the bond angle for H-O-C in alcohols?
    104.5°
  • Why do alcohols have high boiling points?
    Due to hydrogen bonding between molecules
  • Why can smaller alcohols dissolve in water?
    They can form hydrogen bonds with water
  • What is the oxidizing agent that causes alcohols to oxidize?
    Potassium dichromate (K<sub>2</sub>Cr<sub>2</sub>O<sub>7</sub>)
  • What is the product of the partial oxidation of primary alcohols?
    Aldehyde
  • What reagent is used for the partial oxidation of primary alcohols?
    Potassium dichromate (VI) and dilute sulfuric acid
  • What is the condition for the partial oxidation of primary alcohols?
    Warm gently and distill out aldehyde
  • What is the naming convention for aldehydes?
    Ends in -al
  • What is the observation when primary alcohols are oxidized?
    Orange dichromate reduces to green Cr<sup>3+</sup>
  • Write the oxidation equation for propan-1-ol to propanal.
    CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>OH + [O] → CH<sub>3</sub>CH<sub>2</sub>CHO + H<sub>2</sub>O
  • What is the purpose of distillation in organic chemistry?
    To separate an organic product from its mixture
  • What should be done to maximize yield during distillation?
    Collect distillate at desired boiling point
  • Where should the thermometer bulb be placed in a distillation setup?
    At the T junction connecting to the condenser
  • Why does water enter the condenser from the bottom?
    To improve cooling and prevent backflow
  • Why are electric heaters used for heating organic chemicals?
    To prevent fire hazards from naked flames
  • How can the collection flask be cooled to improve yield?
    By placing it in ice
  • What is the product of the full oxidation of primary alcohols?
    Carboxylic acid
  • What are the conditions for full oxidation of primary alcohols?
    Excess dichromate and heat under reflux
  • What is the observation during full oxidation of primary alcohols?
    Orange dichromate reduces to green Cr<sup>3+</sup>
  • What is reflux used for in organic reactions?
    To prevent organic vapors from escaping
  • Why should the end of the condenser never be sealed?
    To prevent gas pressure buildup and explosion
  • What are anti-bumping granules used for?
    To prevent vigorous, uneven boiling
  • What is the product of the oxidation of secondary alcohols?
    Ketone
  • What reagent is used for the oxidation of secondary alcohols?
    Potassium dichromate (VI) and dilute sulfuric acid
  • What is the condition for the oxidation of secondary alcohols?
    Heat under reflux
  • What do ketones end in?
    • one
  • What happens to ketones during oxidation under these conditions?
    No further oxidation occurs
  • How can aldehydes be distinguished from ketones?
    Aldehydes can be oxidized, ketones cannot
  • What is Tollens’ reagent made from?
    Aqueous ammonia and silver nitrate