27) Amines, amino acids and proteins Flashcards

1
Q

What are amines?

A

organic compounds, derived from ammonia, NH3, in which one or more hydrogen atoms have been replaced by a carbon chain or ring

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2
Q

What is the suffix and prefix for primary amines?

A
suffix = -amine (NH2 at end)
prefix = amino- (NH2 not on carbon 1)
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3
Q

When secondary or tertiary amines contain the same alkyl group prefixes _ or _ are used.

A

di-

tri-

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4
Q

When 2 or more different groups are attached to a nitrogen atom the compound is named as a _ of the larger group.

A

N-substituted derivative

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5
Q

The lone pair of electrons on the N of amines can accept a proton to form what type of bond?

A

dative covalent bond

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6
Q

Give 2 equations for the preparation of a primary, aliphatic amine

A

haloalkane + ammonia -> ammonium salt

ammonium salt + aqueous alkali -> primary amine

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7
Q

Why is ethanol as solvent needed for the preparation of a primary, aliphatic amine?

A

prevent substitution of haloalkane by water to produce alcohols

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8
Q

Why is an excess of ammonia needed for the preparation of a primary, aliphatic amine?

A

prevent/reduce further substitution of the amine group

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9
Q

What reagents and conditions are needed for the preparation of aromatic amines e.g. phenylamine?

A
  1. Sn / conc. HCl
  2. Excess NaOH(aq)
    under reflux
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10
Q

Define amino acid

A

organic compound containing both amine, NH2, and carboxylic acid, COOH, functional groups

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11
Q

Give the general formula for an alpha-amino acid

A

RCH(NH2)COOH

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12
Q

amine group + acid ->

A

salt N+H3 + Cl- etc

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13
Q

carboxylic acid group + alkali(aq) ->

A

salt COO-Na+ etc + water

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14
Q

Describe the esterification of carboxylic acids

A

carboxylic acids are esterified by heating with an alcohol in the presence of conc. sulfuric acid
the acidic conditions protonate the basic amine group

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15
Q

What are amides?

A

products of reactions of acyl chlorides with ammonia and amines

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16
Q

Optical isomerism is found in molecules that have a _

A

chiral centre

17
Q

Define chiral centre

A

a carbon atom attached to four different atoms or groups

18
Q

Define enantiomers

A

optical isomers; stereoisomers that are non-superimposable mirror images of each other

19
Q

How can you identify chiral centres?

A

eliminate double bonds, any methyl groups and CH2s

20
Q

Define condensation polymerisation

A

the joining of monomers with the loss of a small molecule e.g. water or HCl
example: lactic acid -> poly(lactic acid) PLA

21
Q

State two types of linkage

A

ester linkage COO and amide linkage CONH

22
Q

What should you be aware of in the base hydrolysis of polyesters and polyamides?

A

COOH groups will react with a base e.g. NaOH(aq) to form COO-Na+

23
Q

What should you be aware of in the acid hydrolysis of polyamides?

A

The NH2 groups will react with an acid e.g. H+(aq) to form N+H3

24
Q

Name 2 features of addition polymerisation

A

monomer with C=C double bond

backbone of polymer is a continuous chain of carbon atoms

25
Q

Name 3 possible features of condensation polymerisation

A

two monomers, each with two functional groups
or
one monomer with two different functional groups
contains ester or amide linkages

26
Q

For what reasons could a molecule be described as an amino acid?

A

amino group and carboxylic acid group attached to the same carbon

27
Q

What symbol is used to indicate a chiral carbon on the structure of a molecule?

A

asterisk, *

28
Q

Name two key properties of amines

A

nucleophile

base-proton acceptor