Alcohols - Exam Questions Flashcards

1
Q

State why tertiary alcohols are not easily oxidised.

A

no hydrogen atom on the central carbon

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2
Q

State the test and result for an aldehyde.

A

Fehling’s solution - turns brick red

negative result = blue

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3
Q

State the advantages of making ethanol by the hydration of ethene.

A
  • fast reaction
  • pure product
  • continuous cycle
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4
Q

State the disadvantages of making ethanol by the hydration of ethene.

A
  • high technology
  • expensive equipment
  • ethene is from non-renewable resources
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5
Q

Outline a mechanism for the dehydration of alcohol to form an alkene in the presence of an acid catalyst.

A

H+ bonds with OH
OH2 breaks off - carbocation
CH breaks to form double bond - H+ ion + alkene

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6
Q

Give a suitable dehydrating agent for a dehydration reaction.

A

concentrated H2SO4

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7
Q

Name the types of reaction illustrated by:
glucose –> ethanol
ethanol –> ethene

A
  • fermentation
  • dehydration
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8
Q

State what must be added to an aqueous solution of glucose so that ethanol is formed.

A

yeast

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9
Q

Give one advantage of using ethanol as a fuel compared with using a petroleum fraction.

A

ethanol is renewable

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10
Q

Which reagent is required for the reaction of a haloalkane to form an alkene.

A

alcoholic hydroxide

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11
Q

State the purpose of the anti-bumping granules.

A

to prevent vigorous boiling

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12
Q

Name the mechanism for the dehydration reaction of an alcohol to form alkenes.

A

elimination

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13
Q

Identify a catalyst for the dehydration of ethanol to form ethene.

A

Concentrated H2SO4

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14
Q

Identify a catalyst and a reagent for converting a vegetable oil into margarine.

A

nickel + hydrogen

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15
Q

State what is meant by the term hydration.

A

addition of water

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16
Q

Give a suitable reagent & reaction conditions for the oxidation of an alcohol to form the carboxylic acid as the major product.

A
  • potassium dichromate in excess
  • concentrated sulfuric acid
  • heat under reflux
17
Q

State three essential conditions necessary to produce a good yield of ethanol from fermentation.

A
  • yeast
  • anaerobic
  • temperature of 30 degrees celsius
18
Q

Name & outline the mechanism for the reaction of a haloalkane to produce an alkene.

A

Elimination: (ethanolic OH)

  • OH attacks C-H adjacent to C-X
  • double bond forms
  • X breaks of, H20 + X-
19
Q

Conditions for the hydration of ethene into ethanol.

A

high temperature + high pressure
SiO2 coated in phosphoric acid (catalyst)