6.1 Arenes Flashcards

1
Q

Why is phenol more reactive than benzene?

A

The p orbital electrons in the O are donated into the delocalised pi system of electrons in the aromatic ring, making it more nucleophilic and electron dense

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2
Q

Rate benzene, phenol and alkene in terms of reactivity from most to least

A

1) Alkene
2) Phenol
3) Benzene

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3
Q

Why is phenol a stronger acid then aliphatic alcohols?

A

Because the ring helps weaken the O-H bond, so the H is more easily lost

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4
Q

Phenol reacts _______ with Na to form ______ ______ + Hydrogen

A

Vigorously to form sodium phenoxide

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5
Q

How can you distinguish between phenol and a carboxylic acid?

A

Phenol has no reaction with carbonates but a carboxylic acid does

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6
Q

What is a carbonyl functional group?

A

C=O

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7
Q

2,4 DNPH reacts with __________ to form an orange precipitate.

A

Aldehydes and ketones

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8
Q

What can Tollens reagent test for?

A

Aldehydes, forms a silver precipitate

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9
Q

How can Brady’s reagent be used to identify ketones and aldehydes?

A

The recrystallised precipitate has a specific melting point which can be compared to known data values

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10
Q

What does NaBH4 do?

A

Reduce carbonyls to alcohols

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11
Q

What ion is produced to reduce carbonyls?

A

H- hydride ion

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12
Q

What happens to a carboxylic acid in water?

A

It dissolves

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13
Q

What is the general structure of an acid anhydride?

A

ROCOCOR

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14
Q

What is the products of acid anhydride + alcohol?

A

Ester and carboxylic acid

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15
Q

How do you esterify phenol?

A

React with acyl chloride ONLY

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16
Q

What does the carbon on a cyanide ion act as?

A

Nucleophile