Carbonyl Compunds (Aldehydes and Ketones) Flashcards

0
Q

What is the strong oxidising agent used in the oxidation of alcohols?

A

Acidified potassium dichromate(VI)

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1
Q

What is the process of oxidation?

A

When the -OH group is oxidised by strong oxidising agents

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2
Q

What happens to the acidified potassium dichromate(VI) during the oxidation of alcohols?

A

Goes from orange to green

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3
Q

What is formed when alcohols are oxidised?

A

A carbonyl compound (aldehyde or ketone) depends on the type of alcohol being oxidised

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4
Q

How is the carbonyl group formed?

A

Two hydrogens are removed - one from the oxygen and one from the carbon

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5
Q

What is required for the oxidation of alcohols to take place?

A

A hydrogen atom on a carbon atom to which a -OH group is also attached

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6
Q

What is formed when a primary alcohol is oxidised?

A

Aldehyde

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7
Q

What happens if a aldehyde gets oxidised itself?

A

Forms a carboxlyic acid

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8
Q

What is formed if a secondary alcohol is oxidised?

A

Ketone

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9
Q

Can you further oxidise a ketone?

A

No as it has no more hydrogen atoms (would involve breaking the C-C bond which is very hard)

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10
Q

What happens when a tertiary alcohol is oxidised?

A

Nothing - tertiary alcohols cannot be oxidised

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11
Q

Why cannot a tertiary alcohol be oxidised?

A

It doesn’t have a hydrogen atom on a carbon atom that is also attached to a - OH group

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12
Q

How can an aldehyde be extracted as a intermediate product?

A

The aldehyde is distilled from the reaction mixture - prevents it from being oxidised further

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13
Q

What are the reagents and conditions for the oxidation of primary alcohols to aldehydes?

A

Heat with acidified potassium dichromate solution; distill

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14
Q

What are the reagents and conditions for the oxidation of primary alcohols to carboxlyic acids?

A

Heat with excess acidified potassium dichromate solution; heat under reflux

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15
Q

What are the reagents and conditions for the oxidation of secondary alcohols?

A

Heat with acidified potassium dichromate solution

16
Q

Why is an excess amount of acidified potassium dichromate solution used in the oxidation of primary alcohols to carboxylic acids?

A

To ensure the reaction goes to completion