Aldehydes and Ketones Flashcards

1
Q

Where is the C=O group on an aldehyde?

A

The last carbon of a molecule

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2
Q

Where is the C=O group on an ketone?

A

One of the inner carbons on the chain

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3
Q

How is an aldehyde formed?

A

Oxidise a 1* alcohol using H+/K2Cr2O7 and distill

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4
Q

How is a ketone formed?

A

Oxidise a 2* alcohol using H+/K2Cr2O7

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5
Q

Give two tests for an aldehyde

A

Tollen’s reagent (ammonical silver nitrate) forms a silver mirror
Fehling’s solution turns brick red

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6
Q

What is the test for a carbonyl group?

A

2,4 DNPH, a yellow/orange ppt forms when an aldehyde or ketone is present

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7
Q

How is an aldehyde reduced?

A

Add NaBH4, a 1* alcohol is formed

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8
Q

How is a ketone reduced?

A

Add NaBH4, a 2* alcohol is formed

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9
Q

Why are aldehydes and ketones prone to nucleophilic attack?

A

The C=O bond group is polar with a large difference in electronegativity

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10
Q

What reaction occurs between HCN and an aldehyde?

A

Nucleophilic addition occurs

This is useful because it lengthens the carbon chain

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11
Q

Why do aldehydes and ketones have a higher BP than alkanes?

A

They have both VDW and dipole-dipole forces since the bond is polar

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12
Q

What is the test for a methyl ketone or an alcohol that can be oxidised to a methyl ketone?

A

Add I2 and NaOH(aq) a yellow ppt forms

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