3.3.8 Aldehydes and ketones Flashcards

1
Q

What are primary alcohols oxidised to

A

Primary alcohols –> Aldehydes –> Carboxylic acids

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2
Q

What are secondary alcohols oxidised to

A

Secondary alcohols –> Ketones

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3
Q

Test(s) for Aldehydes

A

Tollens reagent - silver mirror
Fehlings solution - brick red ppt
Acidified potassium dichromate - orange to green solution

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4
Q

What reduces aldehydes/ketones

A

NaBH4

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5
Q

What are aldehydes and ketones reduced to

A

Aldehyde - Primary alcohol
Ketone - Secondary alcohol

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6
Q

What type of reaction is the reduction of an alcohol/ketone

A

Nucleophilic addition

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7
Q

How to produce hydroxynitriles from aldehydes/ketones

A

Nucleophilic addition
Using KCN
Add dilute acid

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8
Q

Why use KCN instead of HCN (3)

A

HCN is a poisonous gas
HCN is hard to store
HCN is a weak acid and does not completely dissociate into CN- ions in water

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9
Q

How to write reduction reaction

A

[H] instead of H2

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10
Q

Explain why nucleophilic addition reactions of KCN, followed by dilute acid, can produce a mixture of enantiomers.

A

C=O bond is planar
So nucleophile can attack from above or below
With equal probability

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11
Q

Nucleophiles for nucleophilic addition

A

H- or CN-

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