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Examples nomenclature

As noted in Section 1.02.3.2, replacement procedures can be applied to heterocyclic analogues of polycarbocycles named by fusion nomenclature. Examples (48) and (49) show... [Pg.23]

The IUPAC rules for naming aldehydes append the suffix -al to the parent name. The aldehyde carbon is always the first carbon in the chain, so a locant is not necessary. The simplest aldehyde, methanal, is commonly known as formaldehyde, a highly toxic gas used to preserve biological specimens. Ethanal is the next aldehyde, although most organic chemists call it acetaldehyde. 2,2,2-Tri-chloroethanal, more commonly known as chloral, reacts with water to form the sedative chloral hydrate. Phenylmethanal, more commonly known as benzalde-hyde, is used as artificial cherry or almond flavoring. Nomenclature examples of aldehydes are shown in Figure 11.34. [Pg.299]

The IUPAC rules for naming ketones append the suffix -one to the parent name. The position of the ketone carbon is indicated by a locant number. Figure 11.37 gives three nomenclature examples of ketones. The simplest ketone, propanone, is commonly known as acetone. Acetone is an excellent solvent for most organic compounds and is the main ingredient in fingernail polish remover. Acetone is one of the ketone bodies that build up in the bloodstream from excessive metabolism of fats. Because ketones typically have a sweet taste and odor, this can give a patient with ketosis a characteristic acetone breath. ... [Pg.300]

The IUPAC rules name esters as alkyl alkanoates. That is, the portion of the ester derived from the alcohol is named as an alkyl group. The portion of the ester that is derived from the carboxylic acid is named as the conjugate base of that acid. It is easy to distinguish these parts. The half derived from the carboxylic acid has the carbonyl group. Pentyl ethanoate, or pentyl acetate, is one ester used as artificial banana flavoring. Figure 11.51 shows three ester nomenclature examples. [Pg.306]

Number the carbon chain to give the lower number to the highest priority functional group, and then follow all other rules of nomenclature. Examples are shown in Figure B.1. [Pg.1179]

Group of compounds Definition Alternative nomenclature Examples... [Pg.437]


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See also in sourсe #XX -- [ Pg.8 , Pg.9 , Pg.10 , Pg.11 , Pg.12 , Pg.13 ]

See also in sourсe #XX -- [ Pg.4 , Pg.42 ]




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