Alcohols Flashcards

1
Q

What is the alcohols functional group

A

CnH2n+1OH

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2
Q

What does the polar OH allow?

A

Hydrogen bonding in water therefore they are miscible

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3
Q

What is a primary, secondary and tertiary alcohol?

A

Primary - One carbon directly bonded to the carbon atom that is bonded to the OH group
Secondary - two
Tertiary - Three

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4
Q

What are the main methods of preparing alcohols?

A

1) From the corresponding halogenoalkane by heating the halogenoalkane under reflux with sodium bromide solution, which is hydrolysis and occurs by nucleophilic substitution
2) A liquid alcohol can be distilled off by fractional distillation

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5
Q

What is the colour of the flame when alcohols are burnt?

A

Blue

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6
Q

Why is ethanol considered a carbon neutral fuel?

A

It can be formed from fermentation of plant sugars made during photosynthesis. Photosynthesis uses up CO2 in the atmosphere. Less soot given off while burnt as it burns with a clean blue flame

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7
Q

What are the conditions for an alcohol reacting with phosphorus pentachloride PCl5

A

In a fume cupboard, add phosphorus pentachloride to the alcohol

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8
Q

Products?

A

halogenoalkane, POCl3 (phosphorus oxychloride) and HCl

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9
Q

Observations?

A

Misty fumes, solid disappears, exothermic

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10
Q

What are the conditions for an alcohol to react with hydrogen bromide

A

Heat under reflux with HBr - HBr generated in situ from NaBr and H2SO4

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11
Q

Products

A

Halogenoalkane and water

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12
Q

What are the conditions for an alcohol to react with sodium

A

A small piece of sodium metal added to the alcohol

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13
Q

What are the products

A

Sodium alkoxide (H drops off OH and it becomes ONa) and hydrogen

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14
Q

Observations

A

Fizzing

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15
Q

What is acidified potassium dichromate (VI) solution used for

A

The mild oxidation of organic compounds

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16
Q

What is used to acidify the compounds?

A

Sulfuric acid as it is already in its highest oxidation state

17
Q

What happens when a primary alcohol is mildly oxidised?

A

Undergoes oxidation

Alcohol → Aldehyde → Carboxylic acid

18
Q

What are the conditions necessary for the mild oxidation of a primary alcohol

A

Heat with acidified potassium dichromate (VI) solution

19
Q

How do you obtain the carboxylic acid / aldehyde

A

Heat under reflux - Carboxylic acid

Heat and distill - Aldehyde

20
Q

What are the observations?

A

Orange solution → Green solution

21
Q

What happens when you heat a secondary alcohol with acidified potassium dichromate (VI) solution?

A

2º alcohol → Ketone

Orange solution → Green solution

22
Q

Are tertiary alcohols able to be oxidised?

A

No, they are resistant to mild oxidation

23
Q

Write the mild oxidation of butan-2-ol to butanone using [O] to represent the oxidising agent

A

KC 14