4.4 - Alcohols Flashcards

1
Q

What is the functional group of an alcohol

A

-OH

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2
Q

What is the general formula of an alcohol

A

CnH2n+1OH

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3
Q

why are there hydrogen bonds in alcohols

A

Due to the O-H bond which is very electronegative

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4
Q

What is the trend in alcohols with MP and BP and why

A

the longer the chain the higher the BP as there are more induced dipole-dipole forces this means that more energy is required to overcome the bonds.

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5
Q

What is the solubility in alcohols

A

Small alcohols are soluble in water
however long length chains are not soluble in water

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6
Q

are alcohols more or less volatile then their alkane counterpart

A

less

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7
Q

What is a primary alcohol

A

The -OH group is attached to a carbon that is attached to one alkyl group and 2 hydrogen atoms (methanol is an exception but still primary)

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8
Q

what is a secondary alcohol

A

The -OH group is attached to a carbon that is attached to 2 alkyl groups and 1 hydrogen atom

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9
Q

what is a tertiary alcohol

A

○ The -OH group is attached to a carbon that is attached to 3 alkyl groups and no hydrogen atoms

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10
Q

What is the word equation for combustion of alcohols

A

Alcohol + Oxygen -> CO2 + water

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11
Q

Which alcohols can be Oxidised

A

Primary and Secondary

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12
Q

What is the usual oxidising agent

A

a solution of potassium dichromate[K2Cr2O7] acidified with dilute sulfuric acid[H2SO4]

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13
Q

What colour change do you see when an alcohol is oxidised

A

orange to green

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14
Q

What can primary alcohols form when oxidised

A

Aldehydes or carboxylic acids

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15
Q

What can secondary alcohols form when oxidised

A

Ketones

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16
Q

How do you prepare an aldehyde from an alcohol

A

Gently heat a primary alcohol with the [O]
To ensure an aldehyde is formed it is distilled out of the reaction mixture as it is formed to prevent further reaction
The [O] changes colour from orange to green

17
Q

How do you prepare a carboxylic acid from an alcohol

A

Heat a primary acid strongly under reflux with an excess of acidified potassium dichromate a carboxylic acid is formed.
Excess [O] ensures all of the alcohol is oxidised
The reflux ensures any aldehyde formed initially in the reaction also undergoes oxidation

18
Q

How do you prepare a ketone from a secondary alcohol

A

Heat with [O]
To ensure reaction goes to completion the secondary alcohol is heated under reflux
Orange to green colour change

19
Q

what happens when you try to oxidise tertiary alcohols

A

Do not undergo oxidation
[O] stays orange

20
Q

What is the elimination reaction of alcohols known as

A

Dehydration of alcohols

21
Q

What molecule is removed in the dehydration of alcohol

A

H2O

22
Q

What catalyst is used in the dehydration of alcohols

A

Concentrated sulfuric acid or phosphoric acid

23
Q

What is the word equation for the dehydration of alcohols

A

Alcohol + acid catalyst -> alkene + water

24
Q

in the substitution reaction of alcohols what molecule is substituted

A

The -OH group is replaced by a Halogen

25
Q

What is the word equation + conditions for the reaction of alcohols to form haloalkanes

A

Alcohol + hydrogen halide -> Haloalkane + water
alcohol is heated under reflux with sulfuric acid and a sodium halide the hydrogen halide is formed in place here
eg. NaBr + H2SO4 -> NaHSO4 + HBr
the hydrogen halide formed here reacts with the alcohol to form a haloalkane