3.10 The Structure of Benzene Flashcards

1
Q

What is the bond angle in a benzene molecule?

A

120 degrees

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2
Q

Describe the stability of benzene.

A

Benzene is more stable than expected due to its ring of delocalised electrons.

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3
Q

Is benzene classified as an alkene?

A

NO

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4
Q

Why does benzene have a less exothermic enthalpy of hydrogenation than expected?

A

Benzene has a ring of delocalised electrons.

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5
Q

List the three pieces of evidence used to prove benzene is not an alkene

A

Reactivity of bromine, Bond length, Hydration enthalpy.

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6
Q

How does bromine water provide evidence that cyclohexa-1,3,5-triene is not the correct structure for benzene?

A

Benzene does not react with bromine water

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7
Q

Describe the shape of benzene

A

Planar hexagon. All bonds have equal lengths.

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8
Q

What is observed when benzene is added to bromine water?

A

No observation. Benzene does not react with bromine water because it is more stable than an alkene.

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9
Q

How many covalent bonds does each C atom in a benzene ring have?

A

3

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10
Q

What is the chemical test for an alkene?

A

Bromine water, room temperature and shake, Alkenes decolourise bromine water (solution goes from orange to colourless).

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11
Q

The enthalpy change for the hydrogenation of cyclohexene is -120 kJmol-1. What is the theoretical enthalpy change for cyclohexa-1,3,5-triene?

A

-360 kJmol-1 (3 x 120)

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12
Q

What can the enthalpy of hydrogenation be used to prove?

A

That benzene is not an alkene.

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13
Q

What feature of the bonding in benzene distinguishes it from an alkene?

A

It has a ring of delocalised electrons.

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14
Q

Which bond is longer, a C-C bond or a C=C bond?

A

C-C (less attraction)

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15
Q

How does bromine water provide evidence that benzene is not an alkene?

A

Benzene does not react with bromine water

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16
Q

What is the molecular formula of benzene?

A

C6H6

17
Q

Why is cyclohexa-1,3,5-triene considered to be a theoretical molecule?

A

The p-orbitals of adjacent C atoms overlap to form a delocalised ring. The result is benzene.

18
Q

Why was the theoretical enthalpy of hydrogenation of cyclohexa-1,3,5-triene predicted to be more exothermic than that of benzene?

A

Cyclohexa-1,3,5-triene does not account for the delocalised ring of electrons that make benzene more stable and less reactive.

19
Q

Benzene has a regular hexagon shape. What length are it bonds?

A

All its bonds are equal in length. Benzenes bonds are longer than C=C and shorter an C-C bonds

20
Q

What is the enthalpy of hydrogenation?

A

The enthalpy change when one mole of C=C bonds react with hydrogen.

21
Q

How many C atoms does benzene have?

A

6

22
Q

Given that benzene has a ring of delocalised electrons how are its properties different from an alkene?

A

It is more stable and therefore less reactive.

23
Q

What type of molecule is benzene?

A

Aromatic

24
Q

What is the empirical formula of benzene?

A

CH

25
Q

Describe the bonding in benzene.

A

Each C has 3 single covalent bonds. P-orbitals overlap to form a ring of delocalised electrons.

26
Q

Why is benzene less reactive than a molecule that contains C=C bonds?

A

It has a ring of delocalised electrons

27
Q

Why is benzene not classified as an alkene?

A

It has a ring of delocalised electrons.

28
Q

All benzenes bonds are equal in length. What does this suggest?

A

That benzene does not have alternating single and double bonds. It is not an alkene.

29
Q

What is another way of referring to the theoretical molecule cyclohexa-1,3,5-triene?

A

Kekule benzene.
Kekule incorrectly thought that benzene had alternating single and double bonds.

30
Q

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

A

It has a ring of delocalised electrons