Aromatics Flashcards

1
Q

Why is benzene more stable than cyclcohex-1,3,5-triene?

A

Has a higher enthalpy of hydrogenation which means it requires more energy to break the bonds

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2
Q

Why does Benzene having its electron in the p orbital make it more stable?

A

As it forms a ring of delocalised electrons

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3
Q

What is unusual about the bonds in benzene?

A

They are all the same length

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4
Q

What type of reaction does benzene undergo?

A

Electrophillic substitution

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5
Q

What must be drawn when doing a benzene mechanism?

A

The circle becoming a half circle with a +
An arrow from the hydrogen bond going back into the half circle

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6
Q

What are the conditions for the formation of nitrobenzene?

A

Heated at 55°C

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7
Q

When forming nitrobenzene where does the NO2+ come from?

A

H2SO4 + HNO3 -> H2NO3+ + HSO4-
H2NO3+ -> H2O + NO2+

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8
Q

What are the products in the formation of nitrobenzene?

A

Nitrobenzene
H+

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9
Q

What is benzene in terms of acid-base?

A

Lewis base

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10
Q

What is the reaction of Benzene and an acyl chloride called?

A

Friedel-Crafts acylation

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11
Q

What reacts with the acyl chloride to form electrophile?

A

AlCl3

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11
Q

What type of bonding does AlCl3 have?

A

A dative covalent bond (with one of the chlorines) as it want a full outer shell

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11
Q

What is nitrobenzene reduced to?

A

Phenylamine

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