Chapter 14 Flashcards

1
Q

What are the two different ways ethanol can be made

A

Hydration of ethene and fermentation

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2
Q

Properties of methanol

A

Clean burning
Fuel additive in high performance cars
Starting material in many industrial syntheses
Toxic causes severe organ damage then death

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3
Q

Uses of ethanol

A

Alcoholic drinks
Perfumes
Cleaning fluids
Mouthwash
Fuel- up to 10% added to increase octane rating and make fuel burn more cleanly
Added to methanol to make methylated spirits- solvent for removing paints

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4
Q

What is the suffix for an alcohol with two OH groups

A

Diol
*chain name not shorted as diol doesn’t begin with vowel eg butanediol

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5
Q

Properties of alcohol

A

High mp and bp due to hydrogen bonding
Lower volatility compared to alkanes with a similar mass due to hydrogen bonding

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6
Q

How does volatility change as bp changes

A

As volatility increases the bp decreases

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7
Q

Describe and explain the trend in bp of alcohols

A

Bp increases as molecular mass increases ( chain length increases)
Strength of London forces increase due to more surface area contact and hydrogen bonds increase meaning more energy is needed to overcome the bonds

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8
Q

Why do alcohols dissolve in water and what is the pattern

A

Because hydrogen bonds form between the polar OH groups of the alcohol and the water molecule
Solubility decreases as the chain length increases (the first 3 are soluble) because as the molecule increases in size the amount of non polar region increases so solubility decreases

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9
Q

What is a primary alcohol

A

OH group attached to a carbon with two hydrogens and ONE alkyl group
Or three hydrogen atoms in methanol

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10
Q

What is a secondary alcohol

A

OH group attached to a carbon atom bonded to TWO alkyl groups

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11
Q

What is a tertiary alcohol

A

OH group attached to a carbon atom bonded to THREE alkyl groups

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12
Q

Equation for hydration of ethene

A

Ethene + water ——> ethanol

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13
Q

Conditions for hydration of ethene

A

300 degrees c
60 atm
Catalyst = H3PO4

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14
Q

Raw material and type used in hydration of ethene

A

Crude oil
Finite

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15
Q

Hydration of ethene
Type of process
Reaction rate
Purity of ethanol

A

Continuous
Fast
Pure

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16
Q

Equation and conditions for fermentation

A

Glucose ——> ethanol + carbon dioxide
37 degrees c
Atmospheric pressure
Catalyst = zymase ( an enzyme in yeast)

17
Q

Fermentation
Raw material
Raw material type

A

Carbohydrate crops eg sugar
Renewable

18
Q

Fermentation
Type of process
Reaction rate
Purity of ethanol

A

Batch - wait for product to be made remove cleans d begin again
Slow
Impure must be purified by fractional distillation

19
Q

What is the structural formula for alcohol

20
Q

What is the structural formula for an aldehyde

21
Q

What are alcohols oxidised by and what is the colour change when oxidation occurs

A

Acidified Potassium dichromate
Orange to green ( dichromate ions to chromium iii ions)

22
Q

How do you get an aldehyde
What inorganic product is also formed

A

Gently heat a primary alcohol with acidified potassium dichromate
Distil product as formed to avoid any further oxidation
Use an excess of alcohol
Water

23
Q

Why does simple distillation work when producing aldehydes

A

Alcohol has hydrogen bonding so has a high bp, the aldehyde doesn’t so has a lower bp so can be distilled

24
Q

How do you produce a carboxylic acid

A

Heat a primary alcohol under reflux so that it is oxidised twice to form a carboxylic acid from an aldehyde
Use a excess of oxidising agent

25
How does reflux work
The aldehyde evaporates then condenses on the tube and drips back down to go through the second stage of oxidation
26
Define reflux
The continual boiling and condensing of a reaction mixture to ensure that the reaction takes place without the contents boiling dry
27
What occurs during the oxidation of secondary alcohols
Oxidised to produce ketones and cannot be oxidised further
28
What is oxidation
The removal of hydrogen Can’t be further oxidised if there is no hydrogen to remove
29
Can tertiary alcohols be oxidised
No
30
What is dehydration of alcohols What is the reaction called What is required
Alcohol dehydrated to produce an alkene ( h and OH removed from either end and c-c double bond formed) Elimination reaction Acid catalyst H3PO4 or H2SO4
31
What is an example of a substitution reaction How does it occur
Alcohol reacting with hydrogen halides to form haloalkanes Alcohol heated up under reflux with sulphuric acid and a sodium Halide as a hydrogen halide is to dangerous to use as a reactant The hydrogen halide then reacts with the alcohol The swaps with the oh group
32
How do you produce an ester
Alcohol + carboxylic acid in an acid catalyst ( commonly con sulphuric acid ) OH comes off carboxylic acid and h comes off alcohol to produce water and the rest are brought together
33
How do you name an ester
Alcohol provides the alkyl part of name Carboxylic acid provides the alkanoate part of the name