Chapter 14 - Alcohols Flashcards

1
Q

General Formula, Functional group

A

CnH2n+1OH
-OH
name ends in -ol

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2
Q

How are alcohols classified

A

As primary, secondary and tertiary

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3
Q

Primary Alcohols

A

-OH grp is attached to C which is attached to 2 H and one alkyl group

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4
Q

Secondary Alcohols

A

-OH grp is attached to C which is attached to 1 H and two alkyl group

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5
Q

Tertiary Alcohols

A

-OH grp is attached to C which is attached to no H and three alkyl group

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6
Q

What is Methanol classified as

A

Primary Alcohol although technically none

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7
Q

Physical properties of alcohols

A

compared to alkanes they are:
- less volatile
- higher m.p.
- more solubility

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8
Q

how can properties of alcohols be explained

A

Alcohols have polar O-H bond so molecule is polar leading to hydrogen bonding
- stronger bonds so more energy needed so higher b.p. and so less volatile
- polar can dissolve in water (also polar)

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9
Q

as the chain length increases the differences between alkanes and alcohols…

A

….decreases
- the chain length increases so london forces do, therefore the effects of the hydrogen bonds are less significant

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10
Q

reactions of alcohols

A
  • combustion
  • oxidation
  • dehydration
  • substitution
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11
Q

Dehydration

A
  • is any reaction where a H2O molecule is removed from the starting material
  • needs acid catalyst like conc. sulphuric/phosphoric acid & reflux
  • makes alkene
  • elimination reaction
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12
Q

what is heating under reflux

A

when you repeatedly heat a substance then condense it allowing the reaction to take place

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13
Q

substitution

A
  • substitution with halide ions is when alcohols react with hydrogen halides
  • forms haloalkanes
  • reflux with sodium halide, sulfuric acid to make hydrogen halide in situ
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14
Q

why do you make the hydrogen halide in situ?

A

as it’s solid and not toxic

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15
Q

substitution equations

A

CH3CHOHCH3 + NaBr + H2SO4 –> CH3CHBrCH3 + NaHSO4 + H2O

NaBr + H2SO4 <–> NaHSO4 + HBr

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16
Q

3 possible products from oxidation of alcohols

A
  • carboxylic
  • ketone
  • aldehyde
17
Q

oxidation of primary alcohols products

A
  • aldehyde
  • carboxylic acid
18
Q

aldehyde conditons

A
  • Gentle heating & distillation
  • acidified potassium dichromate (ox. agent)
    (H2SO4/K2Cr2O7
  • dichromate ions turn from orange to green chromium (+3) ions
19
Q

carboxylic acid conditions

A
  • reflux
  • excess acidified potassium dichromate (ox. agent)
    (H2SO4/K2Cr2O7
  • dichromate ions turn from orange to green chromium (+3) ions
20
Q

aldehyde eq.

A

C2H5OH + [O] –> C2H4O + H2O

21
Q

carboxylic acid eq.

A

C2H5OH + 2[O] –> CH3COOH + H2O

22
Q

oxidation of secondary alcohols

A
  • makes a ketone
  • reflux
  • excess acidified potassium dichromate (ox. agent)
    (H2SO4/K2Cr2O7
  • dichromate ions turn from orange to green chromium (+3) ions
23
Q

ketone eq.

A

C3H7OH + [O] –> C3H6O + H2O

24
Q

Oxidation of tertiary alcohols

A
  • they are not oxidised
  • no hydrogen bond to be removed