aldehydes and ketones
DESCRIPTION
Aldehydes and Ketones. Structure. They are characterized by the carbonyl functional group (C=O). Carbonyl carbon is sp 2 hybridized; trigonal planar ; bond angles close to 120 °. R = alkyl or aryl group. Aldehydes and ketones undergo nucleophilic addition. - PowerPoint PPT PresentationTRANSCRIPT
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ALDEHYDES AND KETONES
STRUCTURE
They are characterized by the carbonyl functional group (C=O).
Carbonyl carbon is sp2 hybridized; trigonal planar;bond angles close to 120°.
R = alkyl or aryl group
Aldehydes and ketones undergo nucleophilic addition.
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Aldehydes are more reactive than ketones towards nucleophilic attack for both steric and electronic reasons.
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They are less reactive than acyl halides and acid anhydrides, but more reactive than esters, carboxylic acids, and amides.
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NOMENCLATURE
A. AldehydesCommon names are based on names of carboxylic acids; replace -ic acid by -aldehyde.
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NOMENCLATURE
A. Aldehydes
IUPAC names are based on longest chain containing the aldehyde group; name of parent ends in -al and aldehyde carbon is always C1.
A cyclic compound is named as a carbaldehyde.
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NOMENCLATURE
B. Ketones
Common names are generated by naming 2 groups attached to carbonyl carbon (alphabetically) and adding ketone.
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NOMENCLATURE
B. Ketones
IUPAC names are based on longest chain with the carbonyl group; name of parent ends in -one; number the chain in the direction that gives the lowest number to the carbonyl carbon.
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NOMENCLATURE
If other functional groups are present, priority order is:carboxylic acid > acid anhydride > ester > acid halide > amide > nitrile > aldehyde > ketone > alcohol > thiol > amine > ether > alkene > alkyne > halide.
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3-oxobutanal
4-oxobutanoic acid3-methyl-2-cyclohexenone
3,3-dimethyl-2-butanone
2-hexanone
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PHYSICAL PROPERTIES
Boiling points and melting points are relatively moderate due to polarity of carbonyl group and lack of hydrogen bonding.
They are soluble in water up to 4-5 carbons since C=O group is H-bond acceptor. They are soluble in most common organic solvents.
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PREPARATION OF ALDEHYDES
A. Oxidation of Primary Alcohols
B. Ozonolysis of Alkenes
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PREPARATION OF ALDEHYDES
C. Reduction of Acid Chlorides or Esters
Mild reagents are used to prevent over-reduction.
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PREPARATION OF ALDEHYDES
C. Reduction of Acid Chlorides or Esters
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PREPARATION OF ALDEHYDES
C. Reduction of Acid Chlorides or Esters
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PREPARATION OF KETONES
A. Oxidation of Secondary Alcohols
B. Friedel-Crafts Acylation (Aromatic Ketones)
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PREPARATION OF KETONES
C. From Lithium Dialkylcuprates (Gilman Reagents)
Acid chlorides, which have the best leaving group (Cl¯) of the carboxylic acid derivatives, react with R’2CuLi to give a ketone as the product. Esters, which contain a poorer leaving group (¯OR), do not react with R’2CuLi.
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PREPARATION OF KETONES
D. From Hydration of Alkynes
Hydration of terminal alkynes in the presence of Hg2+ gives ketonesNot useful for internal alkynes because mixture results
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