4.2.1 Alcohols Flashcards

(27 cards)

1
Q

what functional group do alcohols contain

A
  • hydroxyl OH
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2
Q

what is the general formula of an alcohol

A
  • CnH2n+1 OH
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3
Q

what are some general differences in physical properties between alcohols and alkanes with the same number of carbon atoms

A
  • alcohols are less volatile, higher mp/bp and greater water solubility
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4
Q

what is the reason for differences in physical properties between alcohols + alkanes with same no of C

A
  • alkanes have non-polar bonds as electronegativity of H and C very similiar
    > alkane = non polar so very weak London forces
  • alcohol has polar O-H bond because of electronegativity difference
    > alcohol = polar so have weak LF + stronger hydrogen bonds between polar O-H
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5
Q

why do alcohols have high mp + are less volatile

A
  • hydrogen bonds between OH require lots of energy to overcome
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6
Q

are alcohols soluble in water + why

A
  • soluble in water
    > hydrogen bonds form between the polar OH group of alcohol and water molecules
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7
Q

what happens to solubility as the hydrocarbon chain in alcohol increases

A
  • solubility decreases
    > influence of the OH polarity decreases and solubility of longer chains decreasw
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8
Q

why are alcohols very good solvents

A
  • can dissolve both polar and non-polar molecules
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9
Q

what are the 3 different ways alcohols can be classified as

A
  • primary
  • secondary
  • tertiary
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10
Q

alcohols can undergo combustion to produce what

A
  • CO2 + H2O
    > releases heat
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11
Q

which types of alcohols can be oxidised

A
  • primary + secondary
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12
Q

what can alcohols be oxidised by

A
  • an oxidising agent
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13
Q

what can primary alcohols be oxidised to

A
  • aldehyde
  • carboxylic acid
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14
Q

how can you make an aldehyde from an alcohol

A
  • oxidation of primary alcohol
  • heat + distill with acidified potassium dichromate (oxidising agent)
    > aldehyde formed
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15
Q

what happens to dichromate ions in oxidation of alcohols

A
  • reduced from orange to green
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16
Q

how do you prevent oxidation of aldehyde into carboxylic acid

A
  • aldehyde removed by distillation as its formed
    > aldehyde has has lower boiling point than alcohol
17
Q

why do aldehydes have lower bp than alcohols

A
  • because they don’t have hydrogen bonds
18
Q

how can you form a carboxylic acid from an alcohol

A
  • primary alcohol heated strongly under reflux with excess of acidified potassium dichromate
19
Q

why do you need excess oxidising agent for formation of carboxylic acid

A
  • to ensure that all of the alcohol is oxidised
20
Q

what does a secondary alcohol oxidise to form

21
Q

how can you form a ketone from an alcohol

A
  • secondary alcohol oxidised under reflux with acidified potassium dichromate
22
Q

what can tertiary alcohols oxidise to from

A
  • nothing
  • tertiary alcohols do not undergo oxidation reactions
23
Q

what is dehydration

A
  • a reaction in which a water molecule is removed from a starting material
24
Q

how do alcohols undergo dehydration + what forms

A
  • alcohol heated under reflux with acid catalyst e.g. conc sulfuric acid or phosphoric acid
  • product is an alkene
25
what is the dehydration of an alcohol an example of
- elimination reaction
26
how are haloalkanes formed from alcohols
- alcohols react with hydrogen halides - alcohol heated under reflux with sulfuric acid + sodium halide (which forms a hydrogen halide) - hydrogen halide reacts with alcohol to form a haloalkanes + water
27
what type of reaction is it when an alcohol turns into a haloalkane
- substitution