amines + amides Flashcards

(50 cards)

1
Q

what is an amine

A
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2
Q

draw out what primary, secondary and tertiary amines would look like

A
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3
Q

why can amines accept H+
and in what conditions

A

it can form a dative covalent bond
in low ph conditions (acidic)

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4
Q

what are amines described as and why

A

bases as they can accept H+
weak base

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5
Q

what is the prefix for amines when there is another functional group on the molecule

A

amino

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6
Q

name this molecule

A

2-aminoethanoic acid

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7
Q

suffix for when amine is the only functional group on the molecule

A

amine
e.g. methyl amine

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8
Q

when do you put an N in front of a part of a molecule with an amine

A

put N in front of the smaller chain

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9
Q

what happens when you react a haloalkane and excess ammonia

A

nucleophilic substitution
forming a primary amine and hydrogen halide

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10
Q

what happens when you react a haloalkane and excess primary amine

A

forms a secondary amine and HCL

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11
Q

show the mechanism for a haloalkane and primary amine reaction

A
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12
Q

what are the 3 ways to synthesise amines

A

Haloalkane + NH3
Haloalkane and primary amine
make nitrile then reduce it

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13
Q

what is the best way to synthesise amines

A

make nitrile then reduce it (add lots pf H’s)

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14
Q

what must the conditions and method for synthesising an amine by making a nitrile then reducing it

A

add haloalkane with on less H than you want
add KCN (spectator K+) in acid
this nitrile reacts with [H]
using hydrogen and nickel catalyst
to form an amine

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15
Q

show an example of a mechanism to turn chloroethane into propanyl amine

A
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16
Q

how to turn nitrobenzene into a phenyl amine (and water)

A

reduce it using [H] and a tin catalyst

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16
Q

show the step by step synthesis of aromatic amines

A
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17
Q

how to add a nitrile onto benzene

A

react with HNO3 and H2SO4

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18
Q

why is at least one of the groups coming off the N on amines a carbon chain

A

if there was 3 H’s then it would be ammonia

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19
Q

what are the 2 main reactions of amines

A

lone pair accepts H+
amines are nucleophile

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20
Q

why do both of the reactions of amines occur

A

because of 1 lone pair of electrons on nitrogen
therefor it attacks as a base

21
Q

show the synthesis of a secondary amine using a primary amine as a nucleophile

21
Q

show the other reaction using amine as a nucleophile

22
Q

how the reaction that occurs when amines are put in low and high pH

A

switches between amine and amine with hydrogen on it

23
put these molecules in order from most to least basic
24
how to identify chiral centres
finding carbon atoms bonded to four different atoms or groups
25
define optical isomers
non-superimposable images of the same molecule
26
define chiral centres
central carbon with 4 different groups attached to it
27
what are the hacks to find chiral centres
there can be multiple on one molcule often found at junctions in amino acids
28
define enantiomers
separates isomers known as R or S R and S are the 2 superimposable image software the same molecule
29
what is an alpha amino acid
1 carbon between carboxylic acid and amine group
30
what is a beta amino acid
2 carbons between carboxylic acid and amine group (won't be given any qs on beta amino acids
31
name this molecule
2-amino-butanoic acid
32
name this molecule
4 - methyl - amine pentanoic acid
32
name this molecule
2 - amine, 4 - hydroxy butanoic acid
33
name this molecule
2,5 - diamino pentanoic acid
34
what happens to carboxylic acids in low and high pH's
35
what happens to amine acids in high and low pH's
35
why are amino acids solid at room temp
bc they are ionic
36
what is the isoelectric point on amino acids
pH at which an amino acid exists primarily as a zwitterion
37
show what a switterion would look like
38
what is the structure of an amide
39
what are the 2 ways to form amides
forming from ammonia and acyl chlorides condensation of peptides
40
what is the mechanism for forming amides from ammonia and acyl chlorides
41
show how the condensation of peptides (amino acids) forms amides
41
draw a primary, secondary and tertiary amide
42
what occurs when you hydrolyse amides
use water for reaction (opposite of condensation reaction)
43
what do you use to hydrolyse amides
NaOH that is aqueous
44
advantage sir using stereoisomers in the synthesis of drugs
fewer side effects reduces cost to produce increases pharmacological effectiveness
45