Chapter 26 Flashcards

(34 cards)

1
Q

What are aldehydes oxidised to?

A

Carboxylic acids

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2
Q

How are aldehydes oxidised?

A

Using dichromate ions under reflux

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3
Q

What are the observations for the oxidation of aldehydes?

A

Orange dichromate ions turn green

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4
Q

What can aldehydes and ketones both be reduced to?

A

Alcohols

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5
Q

What are aldehydes reduced to?

A

Primary alconois

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6
Q

What are ketones reduced to?

A

Secondary alcohols

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7
Q

What nucleophiles are used in nucleophilic addition?

A

NABH4 and HCN

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8
Q

What is used to generate HCN in the lab?

A

Sodium cyanide and sulphuric acid

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9
Q

How do you test for the presence of the carbonyl functional group?

A

Use brady’s reagent a yellow - orange precipitate will form

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10
Q

How do you determine the identity of the aldehyde or the ketone?

A

Recrystalize then melt and compare the melting point to known values

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11
Q

How do you distinguish between aldehydes and ketones?

A

Tollen’s reagent is used.
If an aldehyde is present, a silver mirror Will form
The aldehyde is oxidised

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12
Q

What is a carboxylic acid?

A

Contain functional group COOH
Called carbonyl group

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13
Q

How do you name a carboxylic acid?

A

The suffix -oic acid is added to the end of The longest carbon chain

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14
Q

Explain the solubility of carboxylic acids

A

They Can contain more than one OH . group which means they can form hydrogen bonds to themselves or water molecules

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15
Q

What happens to the solubility of the carboxylic acid as the non polar R group increases?

A

As the length of the chain increases, the solubility decreases

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16
Q

What type of acid are carboxylic acids classed as?

17
Q

What is a carboxylic derivative acid?

A

Compounds that can be hydrolysed to form the parent carboxylic acid

18
Q

What are some examples of carboxylic acid derivatives ?

A

Esters
Acyl chlorides
Acid anhydrides
Amides

19
Q

How do you name an acyl chloride ?

A

After the parent carboxylic acid with the suffix -oyl chloride

20
Q

How can an acyl chloride be prepared from a carboxylic acid?

A

A reaction with the parent carboxylic acid and SOCl2
Thionyl chloride

21
Q

Explain the reactions of acyl chlorides

A

Very reactive
Can easily be converted into amines and esters
Can react with nucleophiles

22
Q

What is a condensation reaction?

A

Two molecules react together to form a larger molecule with the elimination of a small molecule

23
Q

What forms when you react an acyl chloride with an alcohol?

24
Q

What forms when you react an acyl chloride with water?

A

Carboxylic acids
This reaction happens very violently which means that the reactions must be carried out without the presence of water

25
What forms when you react an acyl chloride with ammonia and amines?
Amides The ammonia and amines can act as nucleophiles by donating the lone pair of electrons on the nitrogen
26
How is an acid anhydride formed?
The loss of water between two molecules of carboxylic acid
27
Explain the reactivity of acid anhydrides
They react in a similar way to acyl chlorides but they less reactive making them safer.
28
What is an ester?
They are carboxylic acid derivatives Contain -COO functional group OH replanted by an R group
29
How do you name an ester?
After the parent carboxylic acid with the suffix -oate The alkyl group attached to the COO group is added as a prefix
30
What is an esterification reaction?
The reaction of an alcohol with a carboxylic acid to form an ester
31
How can esters be made?
Reacting alcohols with acyl chlorides or acid anhydrides
32
How do you make a phenyl ester?
By reacting the benzene containing compound with acyl chlorides or acid anhydrides
33
What is acid hydrolysis?
The ester is heated under reflux with an acidic catalyst It will form an alcohol and a carboxylic acid
34
What is alkaline hydrolysis?
Also known as saponification The ester is heated under reflux with an alkaline catalyst Forms a carboxylate ion and an alcohol