17.2.2 - Redox reactions of carbonyl compounds Flashcards

1
Q

What is the compound that reduces aldehydes and ketones back to alcohols?

A

Lithium tetrahydridoaluminate

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2
Q

What are the names of 4 reagents that oxidise aldehydes to carboxylic acids?

A

Acidified potassium dichromate
Fehlings solution
Benedict’s solution
Tollens’ reagent

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3
Q

What is the colour change when an aldehyde reacts with acidified potassium dichromate?

A

Orange to green

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4
Q

What is the colour change when an aldehyde reacts with Fehlings solution?

A

Blue to red precipitate

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5
Q

What is the colour change when an aldehyde reacts with Benedict’s solution?

A

Blue to red precipitate

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6
Q

What is the colour change when an aldehyde reacts with Tollens’ reagent?

A

Colourless to silver mirror

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7
Q

What is formed when a carbonyl compound with a CH3CO group is added to an alkaline solution of iodine, warmed and then cooled?

A

A pale yellow precipitate

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8
Q

What compounds are primary and secondary alcohols oxidised to?

A

Primary = aldehydes and the further to carboxylic acids
Secondary = ketones

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9
Q

What does the reaction between a carbonyl compound and alkaline iodine solution test for?

A

A CH3CO group

Only found in ethanal
Found in all methyl ketones with a carbonyl group on carbon 2

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10
Q

What carbonyl compound will give a positive test when reacting with iodine?

A

Propanone
Butanone
Pentan-2-one

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11
Q

Give an example of a carbonyl compound that will give a negative result when reacted with iodine.

A

Pentan-3-one

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