5.B Aldehydes, ketones
More info: http://www.colby.edu/chemistry/OChem/DEMOS/ketones.html
5.B.1 Description
5.B.1.a nomenclature
5.B.1.b physical properties
5.B.2 Important reactions
5.B.2.a nucleophilic addition reactions at C=O bond
5.B.2.a.i acetal, hemiacetal
5.B.2.a.ii imine, enamine
5.B.2.b reactions at adjacent positions
5.B.2.b.i haloform reactions
5.B.2.b.ii aldol condensation
5.B.2.b.iii oxidation
5.B.2.c 1,3-dicarbonyl compounds, internal hydrogen bonding
5.B.2.d keto–enol tautomerism
5.B.2.e organometallic reagents
5.B.2.f Wolff–Kishner reaction
5.B.2.g Grignard reagents
5.B.3 General principles
5.B.3.a effect of substituents on reactivity of C=O; steric hindrance
5.B.3.b acidity of α hydrogens; carbanions
5.B.3.c α, −unsaturated carbonyl compounds, their resonance structures
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