Aldehydes and ketones Flashcards

1
Q

Where is the carbonyl group located on ketones?

A

They have the carbonyl group on an inner carbon.

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2
Q

What are aldehydes oxidised into?

A

Carboxylic acids.

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3
Q

Which test is able to distinguish between aldehydes and ketones?

A

Add tollen’s reagent ( {Ag (NH3)2}+ ) in a warm water bath. If aldehyde is present a silver mirror is formed as Ag is reduced. Ketone no silver precipitate is formed.

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4
Q

Which reducing agent can reduce aldehydes and ketones?

A

Sodium borohydride (NaBH4) dissolved in methanol and water.

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5
Q

How can you represent oxidising and reducing agents?

A

{O} {H}

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6
Q

What type of alcohols are ketones and aldehydes reduced to?

A

Aldehydes are reduced to primary alcohols, whilst ketones are reduced to secondary alcohols.

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7
Q

What type of mechanism is the reduction of aldehydes and ketones?

A

A nucleophilic addition reaction. The H- ion is a nucleophile and attacks delta positive C.

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8
Q

What type of molecule is formed when potassium cyanide (acidic) reacts with aldehydes or ketones?

A

Hydroxynitriles (a molecule containing OH and CN group).

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9
Q

What happens when we use an unsymmetrical ketone or aldehyde (apart from methanal) in a reaction with potassium cyanide?

A

A mixture of enantiomers are formed.

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10
Q

What risks are associated with potassium cyanide and how to lower these risks?

A

Potassium cyanide is an irritant, therefore, is dangerous if ingested or inhaled. If reacted with moisture it can form toxic gas, hydrogen cyanide. Use goggles, a fume cupboard, gloves.

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