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ALDEHYDES%20AND%20KETONES

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... ketones Methanal (formaldehyde) Ethanal (acetaldehyde) Propanal Pentanal Nomenclature of Aldehydes If the aldehyde group is attached to a ring, ... – PowerPoint PPT presentation

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Title: ALDEHYDES%20AND%20KETONES


1
ALDEHYDES AND KETONES
2
Aldehydes and Ketones
3
d
d-
Most Reactive Group p-electrons polarisation
al aldehydes, one - ketones
Names
Propanal
Methanal (formaldehyde)
Ethanal (acetaldehyde)
Pentanal
4
Nomenclature of Aldehydes
5
If the aldehyde group is attached to a ring,
6
Nomenclature of Ketones
7
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8
Oxidation
9
An aldehyde has a greater partial positive charge
on its carbonyl carbon than does a ketone
10
  • Steric factors contribute to the reactivity of
    an aldehyde
  • The carbonyl carbon of an aldehyde is more
    accessible
  • to the nucleophile
  • Ketones have greater steric crowding in their
    transition
  • states, so they have less stable transition
    states

11
Reactions
  • 1. Redox reactions

12
  • 2. Addition AN

Addition of water
Addition of bisulfite
Bisulfite
13
Addition of NH3
Addition of HCN
Cyanohydrine
14
  • 3. Condensation reactions (addition followed by
    elimination)

Ammonia derivatives
Primary amine
Schiff base
15
Hydroxylamine
Oxime
Hydrazine
Hydrazone
16
Phenylhydrazine
Phenylhydrazone
2,4-dinitrophenylhydrazine
2,4-dinitrophenylhydrazone
17
Aldol condensation
Aldol
18
Reaction with alcohol
Hemiacetal (addition!)
Acetal (condensation!)
19
KetoEnol Tautomerism
20
Oxidation of a Primary Alcohol
21
Reduction by Addition of a Hydride Ion and a
Proton
22
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23
Aldehydes and ketones react with nucleophiles to
form addition products nucleophile addition
reactions
24
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25
Water adds to an aldehyde or ketone to form a
hydrate
26
Hydration of Aldehydes and Ketones
27
Alcohols Under Analogous Reactionwith Aldehydes
and Ketones
  • Product is called a hemiacetal.

28
Example

2CH3CH2OH
HCl
H2O
Benzaldehyde diethyl acetal (66)
29
Reaction with Primary AminesImines
30
If the nucleophile that adds to the aldehyde or
ketone is an O or an N, a nucleophilic
additionelimination reaction will occur
31
Imine (Schiff's Base) Formation
32
Example

CH3NH2
CHNCH3
H2O
N-Benzylidenemethylamine (70)
33
Reaction with Derivatives of Ammonia
34
Reaction with Derivatives of Ammonia
35
Example
H2NNH2
H2O
(73)
36
Example
CCH3
phenylhydrazine
37
An aldol addition product loses water to form an
aldol condensation product
38
Aldol Condensation
NaOH
39
Aldol Addition of Acetaldehyde
Acetaldol(50)
40
Hemiacetal reacts further in acid to yield an
acetal
  • Product is called an acetal.

ROH, H
Product is called a hemiacetal.
41
Formaldehyde
  • formaldehyde cannot form an enolate
  • formaldehyde is extremely reactive
  • toward nucleophilic addition

42
Acrolein
43
Acrolein
44
Acrolein
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