25 Aromatic compounds Flashcards

1
Q

State the 3 pieces of evidence to disprove Kekule’s model

A
  1. Lack of reactivity of benzene
  2. The lengths of the carbon-carbon bond in Benzene
  3. Hydrogenation enthalpies
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2
Q

What is Kekule’s model?

A

6 members ring of carbon atoms joined by alternate single and double bonds

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3
Q

Describe how the lack of reactivity of benzene is evidence to disprove Kekule’s model

A

Kekule’s: Should decolourise bromine in electrophilic addition

Reality:
Does not undergo electrophilic addition
Does not decolourise bromine under normal condition
Hence cannot have any C=C bonds in its structure

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4
Q

Describe how the lengths of C-C bonds in benzene is evidence to disprove Kekule’s model

A

X-ray diffraction determined lengths of bonds
0.139nm = bonds in benzene (in between)
0.153nm = single bond
0.134nm = double bond

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5
Q

Describe hydrogenation enthalpies of benzene is evidence to disprove Kekule’s model

A

Kekule’s: enthalpy change of hydrogenation 3x cyclohexene (-120) : expected -360kJ

Reality: -208kJ, more stable than Kekule’s model
Hence, delocalised model

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6
Q

What are the 6 main features of the delocalised model?

A
  1. Planar, cyclic, hexagonal hydrocarbon containing six carbon atoms and six hydrogen atoms
  2. Each carbon atom uses 3 of 4 Avaliable electron in bonding to 2 other carbon and 1 hydrogen
  3. Each carbon atom has one electron in a p-orbital at right angles to the plane of the bonded carbon and hydrogen atoms
  4. Adjacent p-orbitals electrons overlap sideways, in both directions, above and below the plane of the carbon atoms to form a ring of electron density =
  5. System of pi bonds
  6. 6 electrons in this system are delocalised
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7
Q

How do you name aromatic compounds?

A

Suffixes: Alkyl groups, halogens and nitro
Prefix: If there is a functional group or an alkyl chain with 7 or more carbon atoms

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8
Q

What is the prefix of benzene?

A

Phenyl

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9
Q

What are the common compounds you need to learn which break the rules of the naming rules?

A

Benzoic acid
Phenylamine
Benzaldehyde

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10
Q

State the 4 reactions of benzene

A

Nitration
Halogenation
Alkylation
Acylation

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11
Q

Nitration of benzene reactants, conditions and catalysts and draw full equation

A

Benzene + nitric acid —> nitrobenzene
Catalysts: sulfuric acid
Conditions: heated to 50C (water bath)

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12
Q

What happens if nitration occurs above 50C?

A

Further substitution to dinitrobenzene

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13
Q

Alkylation reaction, reagents, catalysts

A

Electrophilic Substitution of a hydrogen atom in the benzene ring
Benzene + halooalkane —> alkyl + HR
Catalyst: AlCl3

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14
Q

Acylation reaction, reagents, catalysts

A

Electrophilic substitution
Benzene + Acyl chloride —> aromatic ketone + HR
Catalyst: AlCl3

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15
Q

What happens when cyclohexene reacts with bromine?

A

Electrophilic addition
1. The pi bond in Allene contains localised electrons above and below the plane of the 2 carbon atoms in the double bond - high electron density
2. Localised electrons in pi bond induce dipole in the non polar bromine molecule so 1 bromine atom of the Br2 molecule slightly positive and the other bromine atom slightly negative
3. Slightly positive bromine atom enables the bromine molecule to act like an elecrophile

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16
Q

Draw the mechanism for cyclohexene + bromine

A
17
Q

Compare reactivity of aliens to benzene

A
  • Benzene does not react with bromine unless a halogen carrier catalyst is present
  • This is because benzene has delocalised pi electrons spread above and below the plane of the carbon atoms in the ring structure
  • Electron density around 2 carbon atoms in the benzene ring is less than that in a C=C in alkene
  • Bromine non polar so insufficient pi electron density around any 2 carbons in the benzene ring to polarise the bromine molecule so no reaction
18
Q

What is a phenol?

A

-OH (hydroxyl) directly bonded to an aromatic ring

19
Q

Is phenol less or more soluble in water than alcohols?

A

Phenol less soluble in water than alcohols due to the non polar benzene ring
Phenol partially dissociates forming the phenoxide ion and a proton (weak acid)

20
Q

How does phenol’s acidity compare to alcohols and carboxylic acids?

A

Carboxylic acid > Phenol > Alcohol

21
Q

How could you explain phenols acidity?

A
  • Ethanol does not react with NaOH (strong base) or NaCO3 (weak base)
  • Phenols and carboxylic acids react with solution of strong bases
  • Only carboxylic acids react with weak base
22
Q

How could you distinguish between a phenol and carboxylic acid?

A

Sodium carbonate
COOH produces CO2

23
Q
A