6.1 AROMATIC COMPOUNDS AND CARBONYLS Flashcards

1
Q

Benzene

A
  • has the formula C6H6

- has a cyclic structure, with its 6 carbon atoms joined together in a ring

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2
Q

Arenes

A
  • compounds containing a benzene ring
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3
Q

Naming Arenes

A
  • short alkyl side chains, halogens and nitro groups are prefixes to ‘benzene’ when naming arenes
  • we use ‘phenyl’ as a prefix to alkyl side chains greater than 7 carbon atoms long, or alkyl side chains with a functional group
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4
Q

Electrophilic Substitution of Benzene

A
  • results in a hydrogen atom being substituted by an electrophile
  • is a two step mechanism:
    1) the addition of the electrophile to form a positively charged intermediate
    2) the loss of a H+ from the carbon atom attached to the electrophile, which reforms the delocalised ring
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5
Q

Halogen Carriers

A
  • are catalysts that make some compounds into stronger, more polarised electrophiles, in order for them to be able to attack the stable benzene ring
  • accepts a lone pair of electrons from a halogen atom on an electrophile and as the lone pair of electrons is pulled away, the polarisation in the molecule increases, making the electrophile stronger
  • includes aluminium halides and iron halides
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6
Q

Halogenation

A
  • benzene will react with halogens in the presence of an aluminium halide catalyst
  • the catalyst polarises the halogen, allowing one of the halogen atoms to act as an electrophile
  • during the reaction, a halogen atom is substituted in place of a hydrogen atom
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7
Q

Friedel-Crafts Reactions

A
  • are useful for forming C-C bonds in organic synthesis

- are carried out by refluxing benzene with a halogen carrier and either a haloalkane or an acyl chloride

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8
Q

Friedel-Crafts Alkylation

A
  • puts an alkyl group onto a benzene ring using a haloalkane and a halogen carrier
  • the general reaction is:

C6H6 + R-X –> C6H5R + HX

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9
Q

Friedel-Crafts Acylation

A
  • substitutes an acyl group for a H atom on benzene
  • benzene has to be refluxed with an acyl chloride
  • produces phenylketones or benzaldehyde if R=H
  • the general reaction is:

C6H6 + RCOCl —> C6H5COR + HCl

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10
Q

Making Nitrobenzene

A
  • nitrobenzene is made when you warm benzene with concentrated nitric acid and concentrated sulfuric acid
  • sulfuric acid is a catalyst, so it helps to make the nitronium ion, NO2 +, which is the electrophile, and is then regenerated at the end of the reaction mechanism
  • the temperature needs to be kept at 50 degrees celcius
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