alcohols Flashcards

1
Q

how do you name alcohols

A

If there are two or more -OH groups then di, tri are used.

functional groups that need a suffix ending(e.g aldehydes or ketones)g then the OH can be
named with the prefix hydroxy-):

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2
Q

describe oxidation of primary alcohol

A

Potassium dichromate K2Cr2O7
is an oxidising agent
that causes alcohols to oxidise.

primary alcohol turns to aldehyde
Reagent: potassium dichromate (VI) solution and dilute
sulfuric acid.

Conditions: (use a limited amount of dichromate) warm
gently and distil out the aldehyde as it forms:

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3
Q

in the distillation of aldehydes ,how do you maxismise yield

A

In order
to maximise yield collected, only collect the distillate
at the approximate boiling point of the desired
aldehyde and not higher.

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4
Q

why are electric heaters used in the distillation process

A

Electric heaters are often used to heat organic
chemicals. This is because organic chemicals
are normally highly flammable and could set on
fire with a naked flame.

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5
Q

what is the full oxidation of primary alcohol

A

it is in reflux

which is used when heating organic reaction mixtures for long periods.
The condenser prevents organic vapours from escaping
by condensing them back to liquids.

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6
Q

why should you never seal the end of the condenser

A

The build up of gas
pressure could cause the apparatus to explode.

This is true of any
apparatus where volatile liquids are heated including the distillation
set up.

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7
Q

why are anti bumping granules added

A

to prevent vigorous, uneven boiling by making small bubbles
form instead of large bubbles.

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8
Q

describe the oxidation of secondary alcohols

A

Reaction: secondary alcohol –> ketone
Reagent: potassium dichromate(VI) solution and
dilute sulfuric acid.
Conditions: heat under reflux

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9
Q

what are ketones

A

Ketones end in -one
when the is a double C–O bond in the middle of the carbon chain
when more than five carbons involved you add a number

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10
Q

how do you test whether it is a ketone or an aldehyde

A

Tollens’ Reagent
Reagent: Tollens’ reagent formed by mixing
aqueous ammonia and silver nitrate. The
active substance is the complex ion of
[Ag(NH3)2]+

. Conditions: heat gently
Reaction: aldehydes only are oxidised by
Tollens’ reagent into a carboxylic acid. The
silver(I) ions are reduced to silver atoms

Silver mirror coating forms around test tube

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11
Q

How do you test using fehlings solution

A

Fehlings solution contains Cu+ ions
Condition:heat gently
Aldehydes are oxidised into carboxylic acid
Turns from blue to red

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12
Q

Describe reaction of alcohol to alkene

A

Type of reaction is an acid catalysed reaction

Reagent :concentrated sulfuric acid
Conditions:warm after reflux
Role of reagent :dehydrating catalyst

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13
Q

What is a dehydration reaction

A

Removal of a water molecule

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14
Q

What is the acid catalyst in the hydration of alkene to alcohol

A

H3PO4

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15
Q

What are the advantages and disadvantages of fermentation

A

Advantage :
Production using cheap technology
Sugar is a renewable source of energy

Disadvantage:
Ethanol made is not pure and needs to undergo fractional distillation

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16
Q

What are the advantages and disadvantages of industrial formation

A

Advantage :
faster reaction
Purer product

Disadvantages:
High technology needed
Ethene is a non renewable resource

17
Q

How do you test for the presence of carboxylic acid

A

Additional of sodium carbonate
It will fizz and produce carbon dioxide

18
Q

How do you test for the presence of carboxylic acid

A

Additional of sodium carbonate
It will fizz and produce carbon dioxide