Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Elimination reaction of alcohols

Zaitsev s rule as applied to the acid catalyzed dehydration of alcohols is now more often expressed in a different way elimination reactions of alcohols yield the most highly substituted alkene as the major product Because as was discussed in Section 5 6 the most highly substituted alkene is also normally the most stable one Zaitsev s rule is sometimes expressed as a preference for predominant formation of the most stable alkene that could arise by elimination... [Pg.205]

Preparation of Alkenes by Elimination Reactions of Alcohols and Alkyl Halides... [Pg.222]

Unlike many families of molecules, the reactions of alcohols do not fit neatly into a single reaction class. In Chapter 9, we discuss only the substitution and P elimination reactions of alcohols. Alcohols are also key starting materials in oxidation reactions (Chapter 12), and their polar O - H bond makes them more acidic than many other organic compounds, a feature we will explore in Chapter 19. [Pg.326]

Summary Nucleophilic substitution and p elimination reactions of alcohols... [Pg.344]

Alkyloxonium Ions Substitution and Elimination Reactions of Alcohols... [Pg.80]

In Chapters 11 and 12 we return to the presentation of a new functional group the carbon-carbon double bond. This functional group differs from those seen so far in that it hicks strongly polarized covalent bonds. Instead, its reactivity arises from specitil characteristics of electrons in so-called it bonds. The properties of the.se electrons and their consequences are discussed in the next chapter. Chapter 11 is restricted to a general description of alkenes as a compound class and a presentation of methods of preparation of double bonds. Most of the reactions are ones you have already seen, because the major methods of alkene syntheses are the same elimination reactions of alcohols and haloalkanes that were presented in Chapters 7 and 9. Only some finer details have been added. [Pg.367]

Alkyloxonium Ions Substitution and Elimination Reactions of Alcohols A section describing the conversion of the alcohol OH into a leaving group. [Pg.163]

F. ELIMINATION REACTIONS OF ALCOHOLS, ENOLS, AND PHENOLS I. Introduction... [Pg.663]

Zaitsev s rule as applied to the acid-catalyzed dehydration of alcohols is now more often expressed in a different way elimination reactions of alcohols yield the most highly... [Pg.190]


See other pages where Elimination reaction of alcohols is mentioned: [Pg.70]    [Pg.178]    [Pg.42]    [Pg.344]    [Pg.445]    [Pg.445]    [Pg.447]    [Pg.449]    [Pg.409]    [Pg.82]    [Pg.167]    [Pg.663]    [Pg.665]    [Pg.667]    [Pg.669]    [Pg.671]    [Pg.673]    [Pg.675]    [Pg.677]    [Pg.341]    [Pg.492]   
See also in sourсe #XX -- [ Pg.323 , Pg.324 , Pg.325 , Pg.326 ]

See also in sourсe #XX -- [ Pg.379 ]

See also in sourсe #XX -- [ Pg.344 , Pg.344 ]

See also in sourсe #XX -- [ Pg.379 ]

See also in sourсe #XX -- [ Pg.977 ]




SEARCH



Addition-elimination reactions of alcohols with

Alcohol elimination

Alcohol elimination reactions

Elimination Reactions of Alcohols, Enols, and Phenols

Elimination of reactions

Reactions of Alcohols Substitution and Elimination

Reactions of alcohols

© 2024 chempedia.info