amines, amino acids and polymers chp 27 Flashcards

1
Q

define amines

A
  • organic compounds where 1 or more hydrogen atoms from ammonia group (NH3) is replaced with a carbon chain/ring
    ^derived from ammonia
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2
Q

what’s the difference between primary, secondary and tertiary amines

A
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3
Q

how can you name primary amines where the amine group is at the end of the molecule

A
  • adding amine to the end of the nomenclature
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4
Q

How would you name an primary, secondary, tertiary amine where the amine group is not attached to carbon-1

A
  • (number of carbon anime attached to) amino
  • e.g. 2-aminobutane
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5
Q

what do amines act like during chemical reactions

A
  • behave as bases as lone pair of electrons on the nitrogen can accept protons
    ^dative covalent bond formed
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6
Q

How are amines defined as bases

A
  • they neutralise acids to make salts
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7
Q

How can primary amines be formed

what are conditions

A
  • ammonia has lone pair on nitrogen so acts as nucleophile in substitution reaction with haloalkane
  • product is ammonium salt
  • alkali then added to generate primary amine from ammonium salt

ethanol and excess ammonia are conditions

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8
Q
  • what are the conditions needed for the formation of primary amines
  • explain why they are needed
A
  • ethanol used to prevents substitution of haloalkane by water to form alcohols
  • excess ammonia used to reduce further substitutions of amine group to form secondary and tertiary amines
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9
Q

explain the formation of secondary amines

A
  • reacting primary amine with haloalkane to form ammonium salt, then reacting that with NaOH forms secondary amines
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10
Q

explain formation of tertiary amines

A
  • further reaction of secondary amines with haloalkane to produce an ammonium halide salt and then reacting it with NaOH
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11
Q

how is phenylamine (aromatic amine) made

A
  • nitrobenzene is heated under reflux with tin and HCl to form ammonium salt
  • ^this then reacted with excess NaOH to produce aromatic amine

reduction reaction

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12
Q

How can amino acids act as both bases and acids

A
  • amino group can react with acids to form salts
  • the carboxyl group can react with alkalis to from salts and alcohols to from esters
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13
Q

what conditions are needed for amino acids to be esterfied

A
  • heating with alcohol in presence of conc H2SO4
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14
Q

how can amides be formed

A
  • reactions of acyl chloride with ammonia and amines
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15
Q

what are the differences between amides and amines

A

AMINES:

  • derived from ammonia
  • nitrogen atom bonded only to alkyl groups

AMIDE:

  • derived from carboxylic acids
  • nitrogen atom bonded to atleast 1 carbonyl group
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16
Q

difference between primary, secondary and teritary amides

A
17
Q

in what type of molecules are optical isomers found

A

molecules that contain a chiral centre

18
Q

what type of polymerisation do esters and amides undergo

A
  • condensation polymerisation
19
Q

what conditions must be met for condensation polymerisation

A
  • the molecules undergoing polymerisation must contain 2 different functional groups
20
Q

what holds together polymers made from esters

A
  • held together by ester linkages/bonds
21
Q

from which variety of monomers can polyesters be made from

A
  • one monomer containing both carboxylic acid and alcohol
  • 2 monomers, one containing 2 carboxylic acid and one containing 2 alcohol groups
22
Q

how are the ester bonds formed during the formation of the polyesters

A
23
Q

draw how amide linkages/bonds are formed from amino acids

A
24
Q

What 2 variety of monomers could be used for the formation of polyamides

A
  • 1monomer containing both an amine group and a carboxylic acid/acyl chloride group
  • 2 monomers, 1 with 2 amine groups, 1 with 2 carboxylic acids/acyl chloride groups
25
Q

why is used to hydrolyse polyesters and polyamides

A
  • hot aqueous alkali or acid solutions
26
Q

what are the characteristics of addition polymerisation

A
  • monomers contain C=C bond
  • backbone of polymer is carbon chain
27
Q

what are the characteristics of condensation polymerisation

A
  • contain ester or amide bonds
  • can be formed from 2 monomers each with 2 functional groups
  • can be formed from 1 monomer containing 2 different functional groups