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14-1 Ketones, Aldehydes, Amines Unit 14
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14-2 Aldehydes and Ketones The simplest carbonyl compounds are aldehydes and ketones A ketone has two alkyl (or aryl) groups bonded to the carbonyl carbon. An aldehyde has one alkyl (or aryl) group and one hydrogen bonded to the carbonyl carbon.
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14-3 Ketones IUPAC nomenclature requires ketones to be named replacing the –e ending of the alkyl name with –one. Alkane Alkanone
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14-4 Aldehydes Systematic names for aldehydes are obtained by replacing –e with –al. An aldehyde has to be at the end of a chain, thus it is carbon number 1. If the aldehyde is attached to a large unit, the suffix carbaldehyde is used. Cyclohexane carbaldehyde
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14-5 Aldehydes and Ketones Aldehyde and ketone groups can also be named as a substituent on a molecule with another functional group as its root. The ketone carbonyl is given the prefix oxo- and the aldehyde carbonyl is named with the prefix formyl- 2-formylbenzoic acid 3-oxopentanal
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14-6 Aldehydes and Ketones – Common Names The widespread use of carbonyl compounds means many common names are entrenched in their everyday use. Acetophenone
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14-7 Tollen’s Test (Silver Mirror) This type of oxidation reaction is the basis of the most common chemical test for aldehydes. The Tollen’s reagent is added to an unknown compound and if an aldehyde is present, it is oxidized. This process reduces Ag + to Ag which precipitates and sticks to the flask wall forming a mirror. forming a mirror. AgNO 3 +NaOH→AgOH+HNO 3 2AgOH→Ag 2 O+H 2 O Ag 2 O + 4NH 3 + H 2 O → 2Ag(NH 3 ) 2 + + 2OH -
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14-8 Amines Amines are derivatives of ammonia with one or more alkyl groups bonded to the nitrogen. Amines can be classified as primary, secondary or tertiary, meaning one, two or three alkyl groups bonded to the nitrogen respectively. Quaternary ammonium salts have four alkyl groups bonded to the nitrogen and the nitrogen bears a full positive charge.
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14-9 Amines
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14-10 Amines
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14-11 Amines
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14-12 Amines
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