Unsaturated Carbonyl Compound
Upcoming SlideShare
Loading in...5
×

Like this? Share it with your network

Share
  • Full Name Full Name Comment goes here.
    Are you sure you want to
    Your message goes here
    Be the first to comment
No Downloads

Views

Total Views
8,806
On Slideshare
8,800
From Embeds
6
Number of Embeds
1

Actions

Shares
Downloads
97
Comments
0
Likes
2

Embeds 6

http://www.slideshare.net 6

Report content

Flagged as inappropriate Flag as inappropriate
Flag as inappropriate

Select your reason for flagging this presentation as inappropriate.

Cancel
    No notes for slide

Transcript

  • 1. This group of organic compounds containing two functional groups, the carbonyl group and carbon-carbon double bond. In other word we can consider imagery that is including the conjugated diene skeleton as follows.  -- Unsaturated Carbonyl Compound
  • 2. We choose the longest carbon skeleton containing the double bond and the carbonyl group and numbering it whereas the carbon of carbonyl group take the No. 1 in aldehydes, and both the carbonyl group and unsaturated bond the lowest numbers in case of ketones. Then giving the name of aldehyde or ketone as you study in aldehydes and ketones in the first year with designating the position of double bond. Nomenclature:
  • 3.  
  • 4. In the  -unsaturated carbonyl compounds, the carbon-carbon double bond and the carbon-oxygen double bond are separated by just one carbon-carbon single bond; that is, the double bonds are conjugated. Because of this conjugation, such compounds possess not only the properties of the individual functional groups, but certain other properties besides. Structure and properties
  • 5.  
  • 6.  
  • 7.  
  • 8. The general ways to make compounds of this kind includes: the aldol condensation,; dehydrohalogenation of a-halo acids and the Perkin condensation, and Knovenagel condensation. Preparation
  • 9. Examples: Acraldehyde (acrolein) (propenal) : Dehydration of glycerol: By heating glycerol with potassium hydrogen sulphate or with conc. Sulfuric acid.
  • 10. Oxidation of allyl alcohol using MnO 2 : By passing acetaldehyde and formaldehyde vapours over sodium silicate as a catalyst.
  • 11. By direct oxidation of propylene : By pyrolysis of diallyl ether :
  • 12. Crotonaldehyde It is prepared from acetaldehyde by aldol condensation:
  • 13. Interaction of functional group These compounds undergo both electrophilic and nucleophilic addition according to the following: Electrophilic Addition
  • 14. The C=O, -COOH, -COOR , and -CN groups are powerfully electron­-withdrawing groups, and therefore would be expected to deactivate a carbon­-carbon double bond toward electrophilic addition. This is found to be true:
  • 15.  -­ unsaturated ketones, acids, esters, and nitriles are in general less reactive than simple alkenes toward reagents like bromine and the hydrogen halides. But this powerful electron withdrawal, which deactivates a carbon-carbon double bond toward electrophilic addition, at the same time activates toward nucleophilic addition. As a result, the carbon-carbon double bond of an  - ­ unsaturated ketone, acid, ester, or nitrile is susceptible to nucleophilic attack, and undergoes a set of reactions, nucleopbilic addition, that is uncommon for the simple alkenes. This reactivity toward nucleophiles is primarily due, not to a simple inductive effect of these substituents, but rather to their conjugation with the carbon-carbon double bond.
  • 16. Examples:
  • 17. The model of electrophilic addition could be explained in the following Scheme:
  • 18. Intermediate I is the more stable, since the positive charge is carried by carbon atoms alone, rather than partly by the higher electronegative oxygen atom. In the second step of addition, a negative ion or basic molecule attaches itself either to the carbonyl carbon or the b-carbon of the hybrid ion 1.
  • 19. Of the two possibilities, only addition to the b-carbon yields a stable product (Ill), which is simply the enol form of the saturated carbonyl compound. The enol form then undergoes tautomerization to the keto form to give the observed product (IV).
  • 20. Nucleophilic addition Aqueous sodium cyanide converts a,b-unsaturated carbonyl compounds into b-cyano carbonyl compounds. The reaction amounts to addition of the elements of HCN to the carbon-carbon double bond. For example:
  • 21. Ammonia or certain derivatives of ammonia (amines, hydroxylamine, phenyl­hydrazine, etc.) add to a,b-unsaturated carbonyl compounds to yield b-amino carbonyl compounds. For example:
  • 22. These reactions are believed to take place by the following mechanism:
  • 23.  
  • 24. The Michael addition: Of special importance in synthesis is the nucleophilic addition of carbanions to a,b -unsaturated carbonyl compounds known as the Michael addition. Like the reactions of carbanions , it results in formation of carbon-carbon bonds. For example:
  • 25.  
  • 26. The Michael addition is believed to proceed by the following mechanism (shown for malonic ester):
  • 27. The Diels-Alder reaction  -Unsaturated carbonyl compounds undergo an exceedingly useful reaction with conjugated dienes, known as the Diels-Alder reaction. This is an addition reaction in which C-I and C-4 of the conjugated diene system become attached to the doubly-bonded carbons of the unsaturated carbonyl compound to form a six­ membered ring.
  • 28.  
  • 29.