Chapter 18: Q59SP (page 912)
The Wittig reaction is useful for placing double bonds in less stable positions. For example, the following transformation is easily accomplished using a Wittig reaction
Chapter 18: Q59SP (page 912)
The Wittig reaction is useful for placing double bonds in less stable positions. For example, the following transformation is easily accomplished using a Wittig reaction
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Get started for freeUse equations to show the fragmentation leading to each numbered peak in the mass spectrum of cotane-2-one.
Two structures of the sugar fructose are shown next. The cyclic structure predominates in aqueous solution.
(a). Number the carbon atoms in the cyclic structure. What is the fuctional group at C2 in the cyclic form?
(b). Propose a mechanism for the cyclization, assuming a trace of acid is present.
Fructose fructose
(cyclic form)
Use equations to show the fragmentation leading to each numbered peak in the mass spectrum of octane-2-one .
(a) Simple aminoacetals hydrolyze quickly and easily in dilute acid. Propose a mechanism for hydrolysis of the following aminoacetal:
(b) The nucleosides that make up DNA have heterocyclic rings linked to deoxyribose by an aminoacetal functional group. Point out the aminoacetal linkages in deoxycytidine and deoxyadenosine.
(c) The stability of our genetic code depends on the stability of DNA. We are fortunate that the aminoacetal linkages of DNA are not easily cleaved. Show why your mechanism for part (a) does not work so well with deoxycytidine and deoxyadenosine.
Show how you would synthesize the following derivatives from appropriate carbonyl compounds
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