3.3.8 aldehydes and ketones Flashcards

1
Q

what does an aldehyde reduce to?

A

primary alcohol

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2
Q

what does a ketone reduce to?

A

secondary alcohol

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3
Q

what is the reducing agent involved in the reduction of aldehydes and ketones?

A

aqueous sodium borotetrahydride
represented by [H]

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4
Q

why do we use NaBH4?

A

because it is a source of hydride ions and in aqueous solution it is a source of H+ ions

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5
Q

write an equation for the reduction of butanal using [H] to represent reducing agent

A

CH3CH2CH2CHO + 2[H] — CH3CH2CH2CH2OH

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6
Q

what is the name of the mechanism for reduction?

A

nucleophilic addition

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7
Q

how are hydroxynitriles formed?

A

aldehydes and ketones undergo an addition reaction with hydrogen cyanide followed by addition of H2SO4

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8
Q

why don’t we just use HCN instead of KCN and H2SO4 separately?

A

HCN is toxic

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9
Q

what are the reagents used when forming hydroxynitriles?

A

KCN and H2SO4

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10
Q

how do you distinguish between aldehydes and ketones using tollens reagent?

A

using tollens reagent
when tollens reagent is gently warmed with aldehyde the silver mirror is formed

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11
Q

how do you distinguish between aldehydes and ketones using fehlings solution?

A

an aldehyde is oxidised and a colour change from a blue solution to a brick red precipitate is seen
this forms a carboxylic acid

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