Unit 2-Aromatics Flashcards

(11 cards)

1
Q

What is the simplest aromatic hydrocarbon?

A

Benzene (C6H6)

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2
Q

Why is benzene unusually stable?

A

It’s π electrons are delocalised over the ring, forming a conjugated system.

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3
Q

Why does benzene not undergo addition reactions?

A

Addition would break the delocalised π system and reduce stability.

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4
Q

What is a phenyl group?

A

A benzene ring with one hydrogen replaced (-C6H5)

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5
Q

What reactions do benzene rings undergo?

A

Electrophilic substitution reactions.

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6
Q

Why does benzene undergo substitution rather than addition?

A

Substitution preserves the delocalised ring, addition would destroy it.

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7
Q

What catalyst is used for halogenation of benzene?

A
  • AlCl3 or FeCl3 for chlorination
  • AlBr3 or FeBr3 for bromination.
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8
Q

What is alkylation of benzene?

A

Reaction with a haloalkane using AlCl3 to form an alkylbenzene.

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9
Q

What reagents are used for nitration of benzene?

A

Concentrated nitric acid and concentrated sulfuric acid.

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10
Q

What reagent is used for sulfonation of benzene?

A

Concentrated sulfuric acid.

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11
Q

What bonding model describes benzene?

A

sp2 hybridisation, σ bonds in the ring, and a delocalised π system above and below the plane.

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