3.3.5 Alcohols

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39 Terms

1

Name the functional group of alcohols

-OH

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2

What is the name of an alcohols

-of

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3

What is the general formula for an alcohol

CnH2n+1OH

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4

Describe a primary alcohol

With one Carbon side chain

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5

Describe a secondary alcohol

With 2 Carbon side chain

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6

Describe a tertiary alcohol

With 3 Carbon side chains

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7

Why do alcohols have much stronger IMF than alkanes/enes

Due to dipole-dipole and hydrogen bonding

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8

Why do alcohols mix well with water

As they are polar due to H+ bonds

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9

What two methods make alcohols

Fermentation and hydration of ethane

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10

Describe fermentation

A slow process of glucose to an alcohol with yeast in aerobic conditions

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11

Describe hydration of ethane

High temp and pressure fast, reversible reaction with a catalyst

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12

Why is fermentation preferred

It is carbon neutral

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13

Describe the carbon neutral process of fermentation

Photosynthesis, fermentation and combustion

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14

Why is fermentation not seen as carbon neutral

Processes can use fossil fuels which leads to CO2 emissions

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15

What reaction is involved in elimination of alcohols

Dehydration reaction

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16

What are the reagents for elimination of alcohols

Strong acid catalysts (phosphoric acid)

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17

Define oxidising

Loss of electrons

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18

Oxidising agents

Gains electrons so is reduced

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19

What happens when alcohols react with oxidising agents

New functional groups are formed

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20

Describe oxidisation of primary alcohols

Distillation produces an aldehyde, reflux produces carboxylic acid

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21

Describe oxidation of secondary alcohols

Reflux reactions form a ketone

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22

How can you see an oxidation of alcohols

Orange to green colour change

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23

Describe oxidisation of tertiary alcohols

Nothing happens

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24

How are aldehydes formed

When primary alcohols are oxidised partially

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25

Ho ware aldehydes collected

With distillation

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26

What boiling points do aldehydes have and why

Low as they have no hydrogen bonds

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27

What is the purpose of antibumping granules

They promote formation of small bubbles

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28

How does reflux prevent chemicals escaping

By condensing them back into the reaction mixture

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29

Describe the test for a carboxylic acid

Add solution of a carbonate/hydrogen carbonate

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30

Describe the positive result for a carboxylic acid

Gas produced and fizz in from CO2 produced

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31

Give the equation for a carboxylic acid test

H+ (aq) + CO3 2- (aq) —> CO2 (g) + H2O (l)

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32

name te two tests for an aldehyde

Fehling’s reagent and tollen’s reagent

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33

Describe the Fehling’s reagent tests result

A solution to a brick red/orange solution

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34

Give the equation for Fehling’s reagent test

Cu 2+ —> Cu 1+

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35

Describe the positive observation for tollen’s reagent

Silver “mirror” on test tube

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36

Give the equation for Tollen’s reagent

[Ag (NH3)2 ]+ + e- —> Ag (s) + 2 NH3

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37

Describe the test for ketones

cannot be oxidised further so no observations with tests

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38

Give the formula for an aldehyde

CHO

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39

Give the formula for carboxylic acid

COOH

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