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Addition to carbon-hetero multiple

ADDITION TO CARBON-HETERO MULTIPLE BONDS often a proton and the mechanism is... [Pg.1174]

Reactivity factors in additions to carbon-hetero multiple bonds are similar to those for the tetrahedral mechanism of nucleophilic substitution. If A and/or B are electron-donating groups, rates are decreased. Electron-attracting substituents increase rates. This means that aldehydes are more reactive than ketones. Aryl groups are somewhat deactivating compared to alkyl, because of resonance that stabilizes the substrate molecule but is lost on going to the intermediate ... [Pg.1174]

Many of the reactions in this chapter are simple additions to carbon-hetero multiple bonds, with the reaction ending when the two groups have been added. But in many... [Pg.1174]

See other pages where Addition to carbon-hetero multiple is mentioned: [Pg.1172]    [Pg.1176]    [Pg.1178]    [Pg.1180]    [Pg.1182]    [Pg.1184]    [Pg.1186]    [Pg.1188]    [Pg.1190]    [Pg.1192]    [Pg.1196]    [Pg.1198]    [Pg.1200]    [Pg.1202]    [Pg.1206]    [Pg.1208]    [Pg.1210]    [Pg.1212]    [Pg.1214]    [Pg.1216]    [Pg.1218]    [Pg.1220]    [Pg.1222]    [Pg.1224]    [Pg.1226]    [Pg.1228]    [Pg.1230]    [Pg.1232]    [Pg.1234]    [Pg.1236]    [Pg.1238]    [Pg.1240]    [Pg.1242]    [Pg.1246]    [Pg.1248]    [Pg.1250]    [Pg.1252]    [Pg.1254]    [Pg.1256]    [Pg.1258]    [Pg.1260]    [Pg.1262]    [Pg.1264]    [Pg.1266]    [Pg.1268]    [Pg.1270]    [Pg.1272]    [Pg.1274]   


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Addition to carbon

Addition to carbon-hetero multiple bonds

Additives carbon

Carbon addition

Carbon multiple

Carbon multiplicities

Hetero addition

Multiple additions

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