21. Aldehydes and Ketones: Nucleophilic Addition

Naming Aldehydes

21. Aldehydes and Ketones: Nucleophilic Addition

Naming Aldehydes

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Textbook Question

Why are numbers not used to designate the position of the functional group in propanone and butanedione?

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Textbook Question

Name the following ketones and aldehydes. When possible, give both a common name and an IUPAC name. (h) Ph-CH=CH-CHO

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Textbook Question

Give the IUPAC name and (if possible) a common name for each compound. (c)

Give the IUPAC name and (if possible) a common name for each compound. (b)

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Textbook Question

What amino acid is formed using the N-phthalimidomalonic ester synthesis when the following alkyl halides are used in the third step? b. CH3SCH2CH2Br

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Textbook Question

Name the following ketones and aldehydes. When possible, give both a common name and an IUPAC name.

(g) CH3CH2CHBrCH2CH(CH3)CHO

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Textbook Question

What are the systematic names of the following compounds? Indicate the configuration (R or S) of each asymmetric center.

a. d-glucose

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Textbook Question

What are the systematic names of the following compounds? Indicate the configuration (R or S) of each asymmetric center.

b. d-mannose

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Textbook Question

Give a structure that corresponds to the name provided.

(d) E-4-oxopent-2-enal

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Textbook Question

Name the following ketones and aldehydes. When possible, give both a common name and an IUPAC name. (c) CH3(CH2)5CHO

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