4.2.1 Alcohols Flashcards

1
Q

General formula of alcohols

A

CnH2n+1OH

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2
Q

Two methods to make alcohols

A

Fermentation or hydration

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3
Q

How to identify 3 types of alcohol

A

Primary - carbon with OH attached has 1 other C atoms bonded.
Secondary - carbon with OH attached has 2 other C atoms bonded.
Tertiary - carbon with OH attached has 3 other C atoms bonded.

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4
Q

Explanation of solubility

A

Water soluble as they are polar molecules as there is a large difference in electronegativity between C and O. The lone pair on O can H-bond with the H of a water molecule.

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5
Q

boiling point of alcohols compared to equivalent alkanes

A

Higher than other organic molecules. The OH functional group is able to H-bond to the OH group on other alcohol molecules. H-bonds are the strongest intermolecular force meaning more energy is needed to overcome them.

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6
Q

Combustion of alcohols

A

Alcohols make good fuels as lots of energy is released in combustion.
Alcohol + O2 –> CO2 + H2O

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7
Q

What type of reaction occurs between an alcohol and halide ions

A

nucleophilic substitution

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8
Q

Condition for halogenation of an alcohol

A

NaX/H2SO4

where X is the halogen

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9
Q

Equation for reaction of ethanol with HBr and conditions

A

CH3CH2OH + HBr –> CH3CH2Br + H2O

Conditions: NaBr/H2SO4 to produce the HBr

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10
Q

Type of reaction where an alkene is formed from an alcohol

A

Dehydration or elimination

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11
Q

Conditions for forming an alkene from an alcohol

A

heat with concentrated phosphoric acid (H3PO40

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12
Q

Primary alcohols are oxidised to form…

A

aldehydes and/or carboxylic acids

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13
Q

Secondary alcohols are oxidised to form…

A

ketones

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14
Q

Tertiary alcohols are oxidised to form..

A

N/A tertiary alcohols cannot easily be oxidised

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15
Q

Conditions for forming an aldehyde from a primary alcohol

A

heat with acidified potassium dichromate and distil off the product

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16
Q

Conditions for forming a carboxylic acid from a primary alcohol

A

reflux with acidified potassium dichromate

17
Q

Conditions for forming an ketone from a secondary alcohol

A

reflux with acidified potassium dichromate

18
Q

Observation of oxidation with acidified potassium dichromate

A

colour change orange –> green

19
Q

Equation for oxidation of ethanol to ethanal

A

CH3CH2OH + [O] –> CH3CHO + H2O

20
Q

Equation for oxidation of ethanol to ethanoic acid

A

CH3CH2OH + 2[O] –> CH3COOH + H2O

21
Q

Equation for oxidation of ethanal to ethanoic acid

A

CH3CHO + [O] –> CH3COOH

22
Q

Equation for oxidation of propan-2-ol to propanone

A

CH3CH(OH)CH3 + [O] –> CH3COCH3 + H2O

23
Q
Name the following:
CH3CH2CH2OH
CH3CH2CHO
CH3CH2COCH2CH3
CH3CH(OH)CH3
A
  1. propan-1-ol
  2. propanal
  3. pentan-3-one
  4. propan-2-ol
24
Q
Classify the following:
CH3CH2CH2OH
CH3CH2CHO
CH3CH2COCH2CH3
CH3CH(OH)CH3
A
  1. primary alcohol
  2. aldehyde
  3. ketone
  4. secondary alcohol
25
Q
Write the structural formula and classify the following:
2-methylpropan-2-ol
2-methylpropan-1-ol
butanone
butanoic acid
A
  1. CH3C(CH3)(OH)CH3 (tertiary alcohol)
  2. CH3CH(CH3)CH2OH (primary alcohol)
  3. CH3COCH2CH3 (ketone)
  4. CH3CH2CH2COOH (carboxylic acid)