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Cyclohexanes butyl

TLC. 2.5 and 5 pi aliquots of sample and allylestrenol and impurity standard solutions were manually applied in 8 mm bands to HPTLC silica gel plates, which were developed by OPLC with cyclohexane-butyl acetate-chloroform (90 12 2) mobile phase. [Pg.546]

Organic aliphatic acids Methyl isobutyl ketone (MIBK) Ethyl acetate/cyclohexane Butyl acetate Diisopropyl ether 2-Ethyl hexanol... [Pg.353]

Methylpropane Cyclohexane. . . . Cyclohexane. . . . Butyl methyl ether... [Pg.86]

Picoline Mesityl oxide Allyl sulfide Capronitrile Cyclohexane Butyl acetate Isoamyl formate Paraldehyde Toluene... [Pg.140]

Nagata, I. Vapor-Uquid equilibrium data for binary systems, acetone - methyl acetate, methyl acetate -carbon tetrachloride, benzene - butyl acetate, and cyclohexane - butyl acetate. Mem. Fac. Technol., Kanazawa Univ. 1964, 3(3), 197-205. [Pg.3663]

CycJohexyl free radicals, generated by photolysis of t-butyl peroxide in excess cyclohexane, also possess nucleophilic character (410). Their attack on thiazole in neutral medium leads to an increase of the 2-isomer and a decrease of 5-isomer relative to the phenylation reaction, in agreement with the positive charge of the 2-position and the negative charge of the 5-position (6). [Pg.111]

If a disubstituted cyclohexane has two different substituents then the most stable conformation is the chair that has the larger substituent m an equatorial orientation This IS most apparent when one of the substituents is a bulky group such as tert butyl Thus the most stable conformation of cis 1 tert butyl 2 methylcyclohexane has an equatorial tert butyl group and an axial methyl group... [Pg.128]

Make molecular models of the two chair conformations of cis 1 tert butyl 4 phenyl cyclohexane What is the strain energy calculated for each conformation by molecular mechanics Which has a greater preference for the equatorial onentation phenyl or tert butyD... [Pg.472]

Polyisobutylene is readily soluble in nonpolar Hquids. The polymer—solvent interaction parameter Xis a. good indication of solubiHty. Values of 0.5 or less for a polymer—solvent system indicate good solubiHty values above 0.5 indicate poor solubiHty. Values of X foi several solvents are shown in Table 2 (78). The solution properties of polyisobutylene, butyl mbber, and halogenated butyl mbber are very similar. Cyclohexane is an exceUent solvent, benzene a moderate solvent, and dioxane a nonsolvent for polyisobutylene polymers. [Pg.484]

Oxidation catalysts are either metals that chemisorb oxygen readily, such as platinum or silver, or transition metal oxides that are able to give and take oxygen by reason of their having several possible oxidation states. Ethylene oxide is formed with silver, ammonia is oxidized with platinum, and silver or copper in the form of metal screens catalyze the oxidation of methanol to formaldehyde. Cobalt catalysis is used in the following oxidations butane to acetic acid and to butyl-hydroperoxide, cyclohexane to cyclohexylperoxide, acetaldehyde to acetic acid and toluene to benzoic acid. PdCh-CuCb is used for many liquid-phase oxidations and V9O5 combinations for many vapor-phase oxidations. [Pg.2095]

Cl3C(/-BuO) C=NH, Bp3-Et20, CH2CI2, cyclohexane, 70-92% yield. This reagent also forms /-butyl ethers from alcohols. [Pg.246]

Acetone with benzene, butyl acetate, butyl alcohol, carbon tetrachloride, chloroform, cyclohexane, ethanol, ethyl acetate, methyl acetate, acetonitrile, petroleum ether or water. [Pg.37]

Concern for the conservation of energy and materials maintains high interest in catalytic and electrochemistry. Oxygen in the presence of metal catalysts is used in CUPROUS ION-CATALYZED OXIDATIVE CLEAVAGE OF AROMATIC o-DIAMINES BY OXYGEN (E,Z)-2,4-HEXADIENEDINITRILE and OXIDATION WITH BIS(SALI-CYLIDENE)ETHYLENEDIIMINOCOBALT(II) (SALCOMINE) 2,6-DI-important industrial method, is accomplished in a convenient lab-scale process in ALDEHYDES FROM OLEFINS CYCLOHEXANE-CARBOXALDEHYDE. An effective and useful electrochemical synthesis is illustrated in the procedure 3,3,6,6-TETRAMETHOXY-1,4-CYCLOHEX ADIENE. ... [Pg.129]

BUTYL-ETHER 269 C6H12 CYCLOHEXANE -127.917 5.2032E-01 4.4706E-05 31.76... [Pg.379]

The styrene-diene triblocks, the main subject of this section, are made by sequential anionic polymerisation (see Chapter 2). In a typical system cc-butyl-lithium is used to initiate styrene polymerisation in a solvent such as cyclohexane. This is a specific reaction of the type... [Pg.297]


See other pages where Cyclohexanes butyl is mentioned: [Pg.642]    [Pg.386]    [Pg.626]    [Pg.269]    [Pg.498]    [Pg.291]    [Pg.194]    [Pg.1391]    [Pg.894]    [Pg.261]    [Pg.118]    [Pg.672]    [Pg.2842]    [Pg.37]    [Pg.1202]    [Pg.642]    [Pg.386]    [Pg.626]    [Pg.269]    [Pg.498]    [Pg.291]    [Pg.194]    [Pg.1391]    [Pg.894]    [Pg.261]    [Pg.118]    [Pg.672]    [Pg.2842]    [Pg.37]    [Pg.1202]    [Pg.129]    [Pg.129]    [Pg.277]    [Pg.277]    [Pg.501]    [Pg.553]    [Pg.481]    [Pg.493]    [Pg.115]    [Pg.413]    [Pg.360]    [Pg.27]    [Pg.28]    [Pg.29]    [Pg.381]    [Pg.91]   
See also in sourсe #XX -- [ Pg.10 , Pg.168 ]




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Tert-butyl cyclohexane

Tertiary butyl cyclohexane

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