Topic 9- Alcohols Flashcards

1
Q

Alcohols

A

Contain the hydroxyl functional group (-OH)

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2
Q

Primary Alcohol

A

Has one alkyl group bonded to the carbon atom that is bonded to the OH group.

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3
Q

Secondary Alcohol

A

Has two alkyl groups bonded to the carbon atom that is bonded to the OH group.

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4
Q

Tertiary Alcohol

A

Has three alkyl groups bonded to the carbon atom that is bonded to the OH group.

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5
Q

Production of Alcohol by hydration of alkenes

A

Hydration of ethene is carried out by using steam and a catalyst.
CH2=CH2 + H2O(g) –> C2H5OH

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6
Q

Production of Alcohol by hydration of alkenes
Conditions

A
  • catalyst of concentrated phosphoric acid absorbed on a solid silica surface
  • 60 atm pressure
  • 600k temperature
  • excess ethene to give a high yield
  • recycle unreacted ethene and steam back over the catalyst to increase yield.
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7
Q

Production of Alcohol by hydration of alkenes
Mechanism

A
  • electrophilic addition
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8
Q

Production of Ethanol by fermentation

A

Yeast converts sugars such as glucose to ethanol and carbon dioxide.
Ethanol produced by fermentation is separated by fractional distillation and can be used as biofuel.
C6H12O6(aq) –> 2CH3CH2OH(aq) + 2CO2(g)

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9
Q

Production of Ethanol by fermentation
Conditions

A
  • In the presence of yeast
  • Temperature of 35 degrees
  • Anaerobic
  • In aqueous solution
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10
Q

Production of Ethanol by fermentation
Justification of conditions

A
  • Yeast produces an enzyme which converts glucose to ethanol and carbon dioxide.
  • Enzyme in yeast has an optimum temperature of 35 degrees.
  • No air to prevent oxidation of ethanol formed to vinegar
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11
Q

Biofuel

A

A fuel that is made from renewable plant material.

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12
Q

Carbon neutral

A

When activity results in no net emission of carbon dioxide into the atmosphere.

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13
Q

How is ethanol produced by fermentation carbon neutral. (ONLY THEORETICAL)

A

Six molecules of CO2 removed in photosynthesis.
Four molecules of CO2 released in fermentation, Four molecules of CO2 released in combustion per 2 molecules f ethanol burnt.

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14
Q

Oxidation of primary alcohols

A

Oxidized to aldehydes and then further oxidized to carboxylic acids.
- To obtain aldehyde, heat with oxidizing agent and distill.

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15
Q

Equations for oxidation of primary alcohols

A

C2H5OH + [O] –> CH3CHO + H2O
C2H5OH + 2[O] –> CH3COOH + H2O

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16
Q

Oxidation of secondary alcohols

A

Oxidized to ketone
- Heat under reflux with excess oxidizing agent

17
Q

Equations for oxidation of secondary alcohols

A

CH3CH(OH)CH3 + [O} –> CH3COCH3 + H2O

18
Q

Oxidation of tertiary alcohols

A

NO OXIDATION

19
Q

Warm with Tollens` reagent test

A

Aldehyde - forms a silver mirror on tube, (aldehyde is oxidized to the acid)
Ketone - No reaction, remains a colorless solution.