Alcohols Flashcards

(15 cards)

1
Q

Give two reasons why the apparatus shown in the above figure is not safe. 2 marks

A

flask not clamped
allow only the condenser is clamped
sealed system / bung in condenser
allow explanation of effect of bung being there e.g.
pressure build up
not reference to incorrect water direction

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2
Q

State two more mistakes in the way the apparatus is set up in above figure ( oxidation of primary alcohols)

A
  • Direction of water flow through the condenser
  • Thermometer is not needed for the refulx method
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3
Q

State a simple chemical test that distinguishes the propanoic acid from the
propan-1-ol.
Give one observation for the test with each substance

A

Add sodium carbonate
Propanoic acid= we can see bubbles/ effervescene
Propan-1-ol- no visible change

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4
Q

Which compound is produced when 1-phenylethanol reacts with acidified
potassium dichromate(VI)?
A C6H5CH2CH2OH
B C6H5CH2CHO
C C6H5COCH3
D C6H5CH(OH)CH3

A

C- 1-phenylethanol is a secondary alcohol, oxidises to a ketone

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5
Q

Which statement is correct about the production and use of ethanol as a biofuel?
A Biofuel ethanol is produced by the fermentation
of glucose in the presence of yeast and air.
B Biofuel ethanol is purified by fractional
distillation.
C No carbon dioxide is released when biofuel
ethanol is burned.
D Biofuel ethanol burns with a cleaner flame than
ethanol made by hydration of ethene.

A

B

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6
Q

Which compound can be oxidised to form (CH3)2CHCOCH3?
A 2-methylpropan-1-ol
B 2,2-dimethylpropanol
C 2-methylbutan-2-ol
D 3-methylbutan-2-ol

A

D- secondary alcohols oxidise to form ketones

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7
Q

In the UK industrial ethanol is now produced by the direct hydration of ethene.
This process has largely replaced the fermentation method.
Which is a likely reason for this change of method?
A The direct hydration route produces purer ethanol.
B The direct hydration route employs milder conditions.
C The direct hydration route does NOT use a catalyst.
D The direct hydration route produces ethanol by a
slower reaction.

A

A

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8
Q

Describe a test-tube reaction, on the product, to show that the cyclohexanol had been dehydrated.
State what you would observe
2 marks

A

Add bromine water
Colour change observed from orange to colourless

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9
Q

Suggest why sodium carbonate solution was used to wash the distillate. 1 mark

A

Na2CO3 would neutralise the H3PO4

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10
Q

Explain why it is important to open the tap of the separating funnel periodically. ( During separation of products of distillation) 1 mark

A

Prevent build up of gas which would lead to an inc in pressure

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11
Q

Give a property of anhydrous calcium chloride, other than its ability to absorb water, that makes it suitable as a drying agent in this preparation. 1 marks

A

Does not dissolve in/react with the cyclohexene

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12
Q

Describe the apparatus used to remove the drying agent by filtration under reduced pressure. Your description of the apparatus can be either a
labelled diagram or a description in words.

A

Buchner funnel/flat-bottomed funnel containing filter paper
Buchner flask/side-arm flask connected to vacuum pump

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13
Q

Which alcohol can be oxidised by acidified potassium dichromate(VI) but cannot
be dehydrated by heating with concentrated sulfuric acid?
A 2,3-dimethylbutan-2-ol
B 2,2-dimethylpropan-1-ol
C 2-methylpropan-2-ol
D pentan-3-ol

A

B

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14
Q

Describe how the students would use this apparatus to collect a sample of
ethanol.
Include in your answer the functions of the parts of the apparatus labelled
A, B and C. 6 marks

A

Stage 1
* Turn on the water.
* Heat the flask, with a Bunsen burner.
* This causes water and ethanol vapours to be produced.
Stage 2
* Vapours pass up the fractionating column A.
* Water and ethanol are separated in column A.
* Water condenses back into the flask in column A.
Stage 3
* Observe the thermometer at B to keep the temperature at or below the boiling point of
ethanol. Only ethanol vapour (with a little water) passes into the condenser.
* Use the condenser at part C to cool the vapours and condense the ethanol back into a
liquid.

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15
Q
A
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