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Straight-chain

C22H34O2. A straight-chain fatty acid with 5 double bonds. A major component of fish oils and the oils of marine animals, clupeine Protamine class protein found in the sperm and testicles of the herring. On hydrolysis it gives about 90% of argenine. [Pg.102]

The fatty acids occur in nature chiefly as glycerides see fats), which constitute the most important part of the fats and oils, and as esters of other alcohols, the waxes. The naturally occurring fatty acids are mostly the normal straight-chain acids with an even number of carbon atoms. [Pg.173]

C27H55COOH. Glistening scales m.p. 89 C. A straight-chain, saturated fatty acid, that occurs in many natural waxes. [Pg.266]

They can be structured as straight chains as are the normal paraffins or... [Pg.3]

The rings most frequently encountered in crude oils are those having five or six carbon atoms. In these rings, each hydrogen atom can be substituted by a paraffinic alkyl chain that is either a straight chain or branched. [Pg.4]

Paraffins consist mainly of straight chain alkanes, with a very small proportion of isoalkanes and cycloalkanes. Their freezing point is generally between 30°C and 70°C, the average molecular weight being around 350. When present, aromatics appear only in trace quantities. [Pg.285]

The deviation of Gibbs monolayers from the ideal two-dimensional gas law may be treated by plotting xA// 7 versus x, as shown in Fig. III-15c. Here, for a series of straight-chain alcohols, one finds deviations from ideality increasing with increasing film pressure at low x values, however, the limiting value of unity for irAfRT is approached. [Pg.83]

If the dependence on temperature as well as on composition is known for a solution, enthalpies and entropies of adsorption may be calculated from the appropriate thermodynamic relationships [82]. Neam and Spaull [147] have, for example, calculated the enthalpies of surface adsorption for a series of straight-chain alcohols. They find an increment in enthalpy of about 1.96 kJ/mol per CH2 group. [Pg.91]

The behavior of insoluble monolayers at the hydrocarbon-water interface has been studied to some extent. In general, a values for straight-chain acids and alcohols are greater at a given film pressure than if spread at the water-air interface. This is perhaps to be expected since the nonpolar phase should tend to reduce the cohesion between the hydrocarbon tails. See Ref. 91 for early reviews. Takenaka [92] has reported polarized resonance Raman spectra for an azo dye monolayer at the CCl4-water interface some conclusions as to orientation were possible. A mean-held theory based on Lennard-Jones potentials has been used to model an amphiphile at an oil-water interface one conclusion was that the depth of the interfacial region can be relatively large [93]. [Pg.551]

Apart from fatty acids, straight-chain molecules containing other hydrophilic end groups have been employed in numerous studies. In order to stabilize LB films chemical entities such as tlie alcohol group and tlie metliyl ester group have been introduced, botli of which are less hydrophilic tlian carboxylic acids and are largely unaffected by tlie pH of tlie subphase. [Pg.2615]

Other investigations dealt with straight-chain molecules (oi-tricosenoic acid) in which the penultimate and final carbon atoms at the hydrophobic end are connected by a double bond [91, 92]. The material does not polymerize as rapidly as those described before when irradiated by UV light, however, but it is readily polymerized when bombarded with an electron beam. It was thus thought to be an optimal material for the fabrication of electron beam resists. [Pg.2618]

Note that in the compound (CH3)2Si(OH)2 the silicon atom can hold two OH groups, unlike carbon. It is this property that makes the existence of silicones possible. By variation of the compounds and conditions of hydrolysis, straight chains, rings and cross-linked polymers are obtained, for example ... [Pg.190]

Isomerization (rearrangement) of hydrocarbons is of substantial practical importance. Straight-chain alkanes obtained from petroleum... [Pg.101]

The simplest case of structure-property relationships are qualitative rules of thumb. For example, the statement that branched polymers are generally more biodegradable than straight-chain polymers is a qualitative structure-property relationship. [Pg.243]

An area of great interest in the polymer chemistry field is structure-activity relationships. In the simplest form, these can be qualitative descriptions, such as the observation that branched polymers are more biodegradable than straight-chain polymers. Computational simulations are more often directed toward the quantitative prediction of properties, such as the tensile strength of the bulk material. [Pg.308]

Diallylsulfonium salts undergo intramolecular allylic rearrangement with strong bases to yield 1,5-dienes after reductive desulfurization. The straight-chain 1,5-dienes may be obtained by double sulfur extrusion with concomitant allylic rearrangements from diallyl disulfides. The first step is achieved with phosphines or phosphites, the second with benzyne. This procedure is especially suitable for the synthesis of acid sensitive olefins and has been used in oligoisoprene synthesis (G.M. Blackburn, 1969). [Pg.39]

The issue of regioselectivity arises with arylhydrazones of unsymmetrical ketones which can form two different enehydrazine intermediates. Under the conditions used most commonly for Fischer cyclizations, e g. ethanolic HCI, the major product is usually the one arising from the more highly substituted enehydrazine. Thus methyl ketones usually give 2-methy indoles and cycliz-ation occurs in a branched chain in preference to a straight chain. This regioselectivity is attributed to the greater stability of the more substituted enhydrazine and its dominance of the reaction path. [Pg.56]

Unbranched alkanes are sometimes referred to as straight chain alkanes but as we 11 see m Chapter 3 their chains are not straight but instead tend to adopt the zigzag shape portrayed m the bond line formulas introduced m Section 1 7... [Pg.68]

In this case the longest continuous chain has five carbon atoms the compound is named as a derivative of pentane The key word here is continuous It does not matter whether the carbon skeleton is drawn m an extended straight chain form or m one with many bends and turns All that matters is the number of carbons linked together m an uninterrupted sequence... [Pg.72]

Should there be a choice for the fundamental straight chain of a radical, that chain is selected which contains (1) the maximum number of double and triple bonds, (2) the largest number of carbon atoms, and (3) the largest number of double bonds. These are in descending priority. [Pg.5]

Polyethylene. Polymerization of ethylene results in an essentially straight-chain high-molecular-weight hydrocarbon. [Pg.1020]

Oils and gums are nonhighly branched- or straight-chain polymers whose viscosity increases with the degree of polycondensation. [Pg.1023]


See other pages where Straight-chain is mentioned: [Pg.126]    [Pg.202]    [Pg.226]    [Pg.228]    [Pg.282]    [Pg.343]    [Pg.371]    [Pg.195]    [Pg.90]    [Pg.1689]    [Pg.1711]    [Pg.2573]    [Pg.2599]    [Pg.244]    [Pg.134]    [Pg.135]    [Pg.136]    [Pg.136]    [Pg.1046]    [Pg.126]    [Pg.128]    [Pg.130]    [Pg.131]    [Pg.188]    [Pg.172]    [Pg.1]    [Pg.2]    [Pg.157]   
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See also in sourсe #XX -- [ Pg.240 , Pg.241 , Pg.242 ]

See also in sourсe #XX -- [ Pg.21 ]

See also in sourсe #XX -- [ Pg.285 ]

See also in sourсe #XX -- [ Pg.283 ]

See also in sourсe #XX -- [ Pg.261 ]




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Alcohol straight-chain

Aldehydes, straight chain

Alkaloid straight-chain

Alkyl chains, straight

Amino acids straight-chain” pathway

Chain polyethylene waxes, straight

Chains, carbon atoms straight

Formation rate, straight chain

Formation rate, straight chain paraffins

Monolayers of straight chain compounds theoretical ideas

Names of Straight-Chain Alkanes

Organic chemistry straight-chain

Other straight chain amphiphilic compounds

Polymer straight chain active

Potassium straight-chain

Propagation Straight chains

Saturated hydrocarbons straight-chain

Straight

Straight Alkyl Side Chains

Straight Chain Hydrocarbons (A Race)

Straight alkyl chains, number

Straight and Offset Link Chains

Straight chain alkanes

Straight chain alkylated

Straight chain alkylated aromatic compounds

Straight chain reactions

Straight side chain

Straight-Chain Hydrocarbon Nomenclature

Straight-chain Hydrocarbon Nomenclatur

Straight-chain Isomers

Straight-chain alkane isomers

Straight-chain alkanes physical properties

Straight-chain alkanes table

Straight-chain alkanes, names

Straight-chain alkanes, systematic naming

Straight-chain hydrocarbons

Straight-chain hydrocarbons Strong acids

Straight-chain hydrocarbons common

Straight-chain paraffin

Straight-chain pentane

Straight-chain polymer

Straight-chain polymer stability

Straight-chain surfactants, effect

Straight-chained alkanes

Straight-chained heptane

Straight-chained hydrocarbons

Straight-chained structures

Straightness

Water straight-chain alcohols

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