2.7 - Alcohols Flashcards

1
Q

What can alcohols be grouped as?

A

Primary, secondary or tertiary

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2
Q

What is a primary alcohol?

A

1 carbon at functional group

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3
Q

What is a secondary alcohol?

A

2 carbons at functional group

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4
Q

What is a tertiary alcohol?

A

3 carbons at functional group

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5
Q

How is alcohol made by industrial production?

A

Hydration of alkenes in the presence of an acid catalyst, through electrophillic addition.

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6
Q

What conditions are needed to create an alcohol?

A

-phosphoric acid, 300* and 60 atm pressure

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7
Q

How can ethanol be produced?

A

Fermentation - yeast to turn glucose into ethanol

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8
Q

What is the equation for the fermentation of ethanol?

A

C6H12O6 - yeast/40 = 2C2H6O + 2CO2
ethanol is then separated by distilllation which can add cost

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9
Q

Why are biofuels cleaner than petrol?

A

They are renewable because you can grow more plants, they are carbon neutral (CO2 when burnt, aborbed when plants grow)

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10
Q

What are 2 issues with biofuels?

A
  • car engines can’t run on biofuels
  • land used for biofuel - food shortages
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11
Q

What do you get when you oxidise a primary alcohol?

A

Aldehyde
carbon - oxygen double bond and at least 1 carbon hydrogen bond
alkanal (no numbers as carbon must be on end)

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12
Q

What happens when you oxidise an aldehyde?

A

You get a carboxylic acid
c double bond o
carbon - oh double bond

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13
Q

What does oxidation do?

A

Breaks carbon hydrogen bonds but not carbon-carbon bonds
Means you can’t oxidise a tertiary group

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14
Q

What is the oxidising agent for alcohols?

A

acidified potassium dichromate (V)

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15
Q

What do you get if you oxidise a secondary alcohol?

A

Ketones
Double bond carbon to an oxygen atom, and 2 other c-c bonds
alkan-x-one (x= which carbon the ketone lies)

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16
Q

What methods are used to create aldehydes?

A

Distillation
Condenses any reacted aldehyde which forms a gas, into a new flask

17
Q

What method is used to create carboxylic acids?

A

Reflux condensor
Condenses any gases and forces them back into the reaction vessel, aldehydes are returned to the flask to be oxidised again

18
Q

What 2 methods can be used to test between aldehydes or carboxylic acids?

A
  • fehlings solution
  • tollens reagent
19
Q

What is fehlings solution?

A

Cu2+ and is deep blue
Aldehyde - cu2+ oxidises and then reduced to CU+ (brick red)
ketone - no change

20
Q

What is tollens reagent?

A

Diammine silver H ion (AG(NH3)2)+
clear solution
oxidises aldehyde, reduced to solid silver in test tube
does nothing to a ketone

21
Q

What is the equation for the dehydration of alkenes?

A

CnH2n+1OH (H+)= CnH2n +H2O