Benzyl isobutyl ether

Because the transition state of electrophilic addition is rather open or only very weakly bridged, the stereoselectivity is poor, resulting in primarily atactic polymers. Polystyrene and most poly(vinyl ether)s prepared cationically at ambient temperature are atactic with similar proportions of meso and racemic dyads [243,244]. However, meso addition is slightly preferred with vinyl ethers, and varies from 60 to 70% for most monomers, including isobutyl, neopentyl, n-butyl, and ethoxyethyl vinyl ethers [245]. It is higher with benzyl vinyl ether (89%). This tendency to... 

Benzyl phenyl acetate Benzyl phenyl ethyl ether Benzyl priopionate Benzyl salicylate Bensylidine acetone Beta naphthol isobutyl ether... 

Ethylaniline /i-Octyl alcohol j c-Octyl alcohol Butyl sulfide Isobutyl sulfide Benzyl ethyl ether... 

Dicyclohexyl carbodiimide 208-705-7 Benzyl methyl ether 208-706-2 Isobutylbenzene 208-726-1 Ethyl valerate 208-728-2 Ethyl levulinate 208-729-8 Isobutyl butyrate 208-732-4 Amyl hexanoate 208-736-6 Cetyl palmitate... 

The sodium salt of malonate carbanions reacts quantitatively with the living ends of poly(vinyl ether) s to give a stable carbon-carbon bond. This reaction was used to functionalize the ends of Hving poly(isobutyl vinyl ether) or poly(benzyl vinyl ether) with a vinyl ether polymerizable end group supported by a malonate ion (end-capping agent, 7) [151]. 

Ethyl Acetoacetate continued) o-Chloro toluene p-Chloro toluene Anisole o-Cresol Styrene Acetophenone Phenyl acetate m-Xylene o-Xylene p-Xylene p-Methylanisole Phenetole Veratrole Methylheptenone Butyl butyrate Isoamyl propionate Butyl ether sec-Octyl alcohol Butyl sulfide Isobutyl sulfide Indene Mesitylene Propylbenzene Pseudocumene Benzyl ethyl ether... 

Hexyl alcohol 2-Butoxyethanol o-Cresol Isoamyl acetate Heptyl alcohol Benzyl methyl ether Isobutyl isobutyrate Propyl isovalerate Butyl ether sec-Octyl alcohol Isobutyl isovalerate... 

When exposed to ait, the sodium salts tend to take up moisture and form dihydrates. The alkah metal xanthates are soluble ia water, alcohols, the lower ketones, pyridine, and acetonitrile. They are not particularly soluble ia nonpolar solvents, eg, ether or ligroin. The solubiUties of a number of these salts are Hsted ia Table 4. Potassium isopropyl xanthate is soluble ia acetone to ca 6 wt %, whereas the corresponding methyl, ethyl, / -propyl, n-huty isobutyl, isoamyl, and benzyl [2720-79-8] xanthates are soluble to more than 10 wt % (12). The solubiUties of the commercially available xanthates ia water are plotted versus temperature ia Figure 1 (14). 

Honey Allyl phenoxyacetate, phenylaceiate Benzyl cinnamate Carvacryl acetate Cinnamyl butyrate p-Cresyl acetate p-Cresyl ethyl ether /rt-Cresyl phenylaceiate />-Cresyl phenylaceiate Cyclohexyl phenylacctate Ethyl phenoxyacetate. phenylaceiate Guaiol phenylaceiate Isobutyl phenylaceiate Linalyl butyrate Methyl phenylaceiate Phenethyl acetate, butyrate, phenylaceiate Phenylacetic acid Propyl phenylaceiate Santalyl phenylaceiate. 

Propyl chloride Chlorobenzene. Bromobenzene. a-bromnaphthalene Ethyl ether. , Ethylisoamyl ether Phenetol.. . Anisol. . . Ethyl acetate. Isobutyl acetate Ethyl benzoate Isobutyl alcohol Ethyl alcohol. Allyl alcohol. Methyl alcohol Benzyl alcohol. Acetone. . . Acetophenone. ... 

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