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The reaction must be carried out in the absence of direct sunlight, since sunlight causes direct addition of the halogen to the hydrocarbon, particularly if the latter is warm benzene, for example, yields the hexahalide ... [Pg.533]

Whether an element is the source of the cation or anion in an ionic bond depends on several factors for which the periodic table can serve as a guide In forming ionic compounds elements at the left of the periodic table typically lose electrons giving a cation that has the same electron configuration as the nearest noble gas Loss of an elec tron from sodium for example yields Na which has the same electron configuration as neon... [Pg.11]

In addition to being regioselective alcohol dehydrations are stereoselective A stereo selective reaction is one m which a single starting material can yield two or more stereoisomeric products but gives one of them m greater amounts than any other Alcohol dehydrations tend to produce the more stable stereoisomer of an alkene Dehydration of 3 pentanol for example yields a mixture of trans 2 pentene and cis 2 pentene m which the more stable trans stereoisomer predominates... [Pg.205]

Nitroparaffins add 1,4 to conjugated systems methyl vinyl ketones, for example, yield the corresponding y-nitro ketone, which can be reduced to a y-nitro alcohol (48). More than one vinyl group may react with primary nitroparaffins (49). [Pg.100]

Ttinitroparaffins can be prepared from 1,1-dinitroparaffins by electrolytic nitration, ie, electrolysis in aqueous caustic sodium nitrate solution (57). Secondary nitroparaffins dimerize on electrolytic oxidation (58) for example, 2-nitropropane yields 2,3-dimethyl-2,3-dinitrobutane, as well as some 2,2-dinitropropane. Addition of sodium nitrate to the anolyte favors formation of the former. The oxidation of salts of i7k-2-nitropropane with either cationic or anionic oxidants generally gives both 2,2-dinitropropane and acetone (59) with ammonium peroxysulfate, for example, these products are formed in 53 and 14% yields, respectively. Ozone oxidation of nitroso groups gives nitro compounds 2-nitroso-2-nitropropane [5275-46-7] (propylpseudonitrole), for example, yields 2,2-dinitropropane (60). [Pg.101]

Certain organic compounds form reversible gels with poly(vinyl alcohol). Congo red, for example, yields a red gel that melts sharply at about 40°C. Other organic compounds that form temperature-reversible complexes with PVA include a2o dyes, resorcinol, catechol, and gaUic acid (168—170). [Pg.481]

Apply sample followed by 5% potassium carbon- [16] ate solution in aqueous acetone, dry, apply 50% methyl iodide in acetone. Allow to react for 3 h at 50 °C in an atmosphere of methyl iodide — acetone (1 + 4), dry and develop. Oleanonic acid, for example, yields its methyl ester. [Pg.70]

If the particle leaves the box through the left border, jumping to cell -2, for instance, then again applying the bitwise AND between new coordinate and mask (the mask is given simply by the number of the last cell in the box, 7 in this example) yields the correct new periodic position, i.e., in cell 6. [Pg.568]

We recall, from equations 2.8 and 2,9, that only 32 so-called legal rules (out of the 256 total possible rules that can be defined), leave the zero-state a — 0 unchanged and are such that reflection-symmetric local states - 100 and 001 , for example - yield the same values. We now examine the patterns generated by these types of rules. [Pg.54]

The simplest synthetic polymers are those that result when an alkene is treated with a small amount of a radical as catalyst. Ethylene, for example, yields polyethylene, an enormous alkane that may have up to 200,000 monomer units incorporated into a gigantic hydrocarbon chain. Approximately 14 million tons per year of polyethylene is manufactured in the United States alone. [Pg.240]

Ethylene is not unique in its ability to form a polymer. Many substituted ethyl-enes, called vinyl monomers, also undergo polymerization to yield polymers with substituent groups regularly spaced on alternating carbon atoms along the chain. Propylene, for example, yields polypropylene, and styrene yields polystyrene. [Pg.241]

Amines are converted into alkenes by a two-step process called the Iiofnunn elimination. SN2 reaction of the amine with an excess of CH3I in the first stej yields an intermediate that undergoes E2 reaction when treated with silvei oxide as base. Pentylamine, for example, yields 1-pentene. Propose a structim for the intermediate, and explain why it undergoes ready elimination. [Pg.407]

Fischer s original method for conversion of the nitrile into an aldehyde involved hydrolysis to a carboxylic acid, ring closure to a cyclic ester (lactone), and subsequent reduction. A modern improvement is to reduce the nitrile over a palladium catalyst, yielding an imine intermediate that is hydrolyzed to an aldehyde. Note that the cyanohydrin is formed as a mixture of stereoisomers at the new chirality center, so two new aldoses, differing only in their stereochemistry at C2, Tesult from Kiliani-Fischer synthesis. Chain extension of D-arabinose, for example, yields a mixture of D-glucose and o-mannose. [Pg.994]

The parent dibenzotriazepine behaves as a masked diazonium salt hydriodic acid, for example, yields 2 -iodobiphenyl-2-amine (1 a) and hydrobromic acid in the presence of copper powder gives the corresponding bromo compound lb.331... [Pg.453]

An interpretation based on frontier molecular orbital theory of the regiochemistry of Diels Alder and 1,3-dipolar cycloaddition reactions of the triazepine 3 is available.343 2,4,6-Trimethyl-benzonitrile oxide, for example, yields initially the adduct 6.344... [Pg.458]

Primary and secondary aliphatic amines, morpholine and 2-methylaziridine and aniline and even the sterically hindered 2.2,6,6-tetramethylpiperidine readily react with 6-bromo-trithiadiazepine 7, in certain cases in the presence of /V./V-diisopropylethylamine, at room temperature by substitution of the bromine atom ammonia, for example, yields trithiadiazepin-6-amine 22 (R1 = R2 = H). There is compelling evidence that these reactions proceed by an elimination-addition mechanism via the heteroaryne, trithiadiazepyne 21.391... [Pg.484]

In practice, variations in yield factors are often observed for a given organism in a given medium. For example, yield coefficients often vary with growth rate. An explanation for these variations comes from a consideration of the fate of substrate in the cell, which can be divided into three parts ... [Pg.37]

Olefin metathesis of vinylboronates [102] and allylboronates [103, 104] has been investigated over the past few years because organoboranes are versatile intermediates for organic synthesis. Cross metathesis of vinylboronate 108 and 2-butene 109, for example, yields the boronate 110, which can be converted to the corresponding vinyl bromide 111 with high Z selectivity. Vinyl iodides can be obtained analogously. It should be noted that vinyl bromides and vinyl... [Pg.255]

Clenbuterol, for example, yields pink-colored chromatogram zones on a light background. [Pg.61]

Peptides, for example, yield chloramine derivatives on exposure to chlorine gas these derivatives oxidize o-toluidine to a blue semiquinonoid dyestuff in the presence of acetic acid. [Pg.113]

A detailed study of two rare-earth metals under one set of reaction conditions, for example, yielded the two composition phase diagrams, shown in Fig. 14.2, for the Fu and La thiophosphate systems [3]. To prepare these phase diagrams, we varied the alkah metal, the rare-earth metal, and the phosphorous concentration to kept the sulfur concentration constant We prepared similar studies in... [Pg.212]

When this procedure is applied to the data shown for polystyrene in Fig. 116 and to those for polyisobutylene shown previously in Fig. 38 of Chapter VII, the values obtained for t/ i(1 — /T) decrease as the molecular weight increases. The data for the latter system, for example, yield values for this quantity changing from 0.087 at AT-38,000 to 0.064 at ilf = 720,000. This is contrary to the initial definition of the thermodynamic parameters, according to which they should characterize the inherent segment-solvent interaction independent of the molecular structure as a whole. [Pg.537]

A single metal may be extracted from several minerals. Thus there are many minerals of copper, such as chalcocite, bornite, chalcopyrite, cuprite, native copper, and malachite one or more of these may occur in an individual deposit. Also, more than one metal may be obtained from a single mineral stannite, for example, yields both copper and tin. A mineral deposit, therefore, may yield several metals from different minerals. [Pg.37]

That resonance stabilization of intermediate biradicals is important in determining the efficiency of decarbonylation follows from the following examples yielding benzyl radicals upon loss of carbon monoxide(57) ... [Pg.389]

A recent report indicates that thiophenes (not benzothiophenes) may be formed from alkyl phenyl ketones by treatment with a slight excess of thionyl chloride in the cold.58 Propiophenone, for example, yields 3,4-dibenzoyl-thiophene (47). Adipic acid and related carboxylic acids yield thiophene derivatives upon treatment with thionyl chloride in the presence of pyridine.59... [Pg.63]


See other pages where Examples yield is mentioned: [Pg.46]    [Pg.309]    [Pg.367]    [Pg.238]    [Pg.156]    [Pg.215]    [Pg.319]    [Pg.480]    [Pg.164]    [Pg.168]    [Pg.271]    [Pg.35]    [Pg.201]    [Pg.199]    [Pg.148]    [Pg.240]    [Pg.84]    [Pg.361]    [Pg.198]    [Pg.145]    [Pg.328]   
See also in sourсe #XX -- [ Pg.206 ]




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Examples percent yield

HDPE UHMWPE examples of stress at yield retention () versus sub-zero temperatures (C)

HDPE examples of stress at yield retention () versus temperature (C)

PBT examples of stress at yield retention () versus temperature (C)

POM examples of stress at yield retention () versus temperature (C)

Stress at yield examples (MPa)

Yield Based Planning Example of a Single Refinery

Yield strain example problem

Yield strain worked examples

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