Aldehydes and Ketones Flashcards

1
Q

How is the solubility of carbonyls decided?

A

The smaller the molecule the more soluble it is in water as it can form hydrogen bonds with water

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2
Q

What conditions and reagents are needed to oxidise an aldehyde to a carboxylic acid?

A

acidified potassium dichromate and under reflux

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3
Q

How can you test for an aldehyde and what are the positive observations?

A

You can test with Tollen’s reagent and the positive result is a silver mirror>

You can use Fehling’s solution and the positive result is a red ppt.

Acidified potassium dichromate turns from orange to green

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4
Q

Can ketones be oxidised?

A

No

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5
Q

How can you reduce ketones and aldehydes to secondary and primary alcohols respecitively?

A

Use aqueous NaBH₄

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6
Q

What products are formed from the oxidation of a primary alcohol?

A

Aldehyde and water

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7
Q

Why is a racemate is formed?

A

The carbonyl group is planar so the nucleophile can attack from either side of the double formed so both enantiomers are formed evenly.

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8
Q

Why are longer ketones not soluble in water?

A

The rest of the molecule gets in the way of the hydrogen bonds and breaks them.

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9
Q

What to remember when drawing reflux equations for primary alcohols?

A

The double oxidising agent 2[O]
Structural formula
Water at the end

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10
Q

What do anti bumping granules do?

A

They form smaller bubbles and prevent larger bubbles

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