Hydrocarbon group

Hydrocarbon groups (FIA method) NF M 07-024 ISO/DIS 3837 ASTM D 1319 Chromatography on silica gel with fluorescent indicators... 

Sheppard N and De La Cruz C 1998 Vibrational spectra of hydrocarbons adsorbed on metals. Part II. Adsorbed acyclic alkynes and alkanes, cyclic hydrocarbons including aromatics and surface hydrocarbon groups derived from the decomposition of alkyl halides, etc Adv. Catal. 42 181-313... 

Ba.se Catalyzed. Depending on the nature of the hydrocarbon groups attached to the carbonyl, ketones can either undergo self-condensation, or condense with other activated reagents, in the presence of base. Name reactions which describe these conditions include the aldol reaction, the Darzens-Claisen condensation, the Claisen-Schmidt condensation, and the Michael reaction. 

Phosphate Esters. A variety of phosphate esters are used as synthetic lubricants, particularly because of their good fire resistance. They have the general formula OP(OR)2, where R may represent a variety of aryl or alkyl hydrocarbon groups containing four or more carbon atoms to give three broad classes triaryl, trialkyl, and aryl alkyl phosphates (37,38). 

Collectors ndFrothers. Collectors play a critical role ia flotation (41). These are heteropolar organic molecules characterized by a polar functional group that has a high affinity for the desired mineral, and a hydrocarbon group, usually a simple 2—18 carbon atom hydrocarbon chain, that imparts hydrophobicity to the minerals surface after the molecule has adsorbed. Most collectors are weak acids or bases or their salts, and are either ionic or neutral. The mode of iateraction between the functional group and the mineral surface may iavolve a chemical reaction, for example, chemisorption, or a physical iateraction such as electrostatic attraction. 

The functional group ia collectors for nonsulfide minerals is characterized by the presence of either a N (amines) or an O (carboxyUc acids, sulfonates, etc) as the donor atoms. In addition to these, straight hydrocarbons, such as fuel oil, diesel, kerosene, etc, are also used extensively either as auxiUary or secondary collectors, or as primary collectors for coal and molybdenite flotation. The chain length of the hydrocarbon group is generally short (2—8 C) for the sulfide collectors, and long (10—20 C) for nonsulfide collectors, because sulfides are generally more hydrophobic than most nonsulfide minerals (10). 

Esters 4.337 - 0.230N -149.13-1- 18.695N If hydrocarbon groups have isoconfiguration, see ... 

The carbonate groups are polar but separated by aromatic hydrocarbon groups. 

Both the chemical solubility and the electrical properties are consistent with those expected of a lightly polar polymer, whilst reactivity is consistent with that of a polymer containing hydrolysable carbonate ester linkages partially protected by aromatic hydrocarbon groupings. The influence of these factors on specific properties is amplified in subsequent sections. 

Hydrocarbons are segmented into a variety of categories. Each category possesses a distinct molecular profile and, in turn, set of chemical and physical properties. Each class of hydrocarbons therefore has historically served different markets. Crude petroleum is composed of four major hydrocarbon groups paraffins, olefins, naphthenes, and aromatics. 

A common class of weak bases consists of the organic molecules known as amines. An amine can be considered to be a derivative of ammonia in which one or more hydrogen atoms have been replaced by hydrocarbon groups. 

An amine is a derivative of ammonia, NH3, in which one or more of the hydrogen atoms have been replaced by a hydrocarbon group (e.g., CH3, C2H5). Amines can be classified according to the number... 

In a ketone, two hydrocarbon groups (alkyl or aromatic) are bonded to the central carbon atom, giving the general structure... 

R can be any hydrocarbon group or, in the simplest case, formaldehyde, a second hydrogen atom ... 

As usual, R is a hydrocarbon group or, in the simplest case, a hydrogen atom. The acidic hydrogen atom is the one bonded to oxygen. The IUPAC name of a carboxylic add can be obtained by substituting the suffix -oic acid for the final e in the name of the corresponding alkane. In practice, such names are seldom used. For example, the first two members of the series are commonly referred to as formic add and acetic add. 

When the number of hydrocarbon groupings is sufficiently high, one could rank the hydrocarbon groupings according to the kinetic constant, and replace the sum in Eq. (16) by a Laplace integral... 

The metathesis of acyclic alkenes substituted with other hydrocarbon groups, such as cycloalkyl, cycloalkenyl, or aryl groups, has also been observed. For instance, styrene is converted into ethene and 1,2-diphenyl-ethene (stilbene) (9, 9a). 

Recently, enantiomerically pure vinylic sulfoximines have been shown to undergo effective and highly stereocontrolled conjugate addition of hydrocarbon groups using organocopper reagents108. 

Because the types of carbon-carbon bonds present in the molecule tend to dominate its properties, an aliphatic hydrocarbon is first classified as an alkane, alkene, or alkyne. Then the longest chain of carbon atoms is used to form the root of the name. Other hydrocarbon groups attached to the longest chain are named as side chains. 

The substituents are listed in alphabetical order (disregarding the Greek prefixes) and attached to the root name. The names of substituents other than hydrocarbon groups are discussed more fully in Chapter 19 (see Toolbox 19.1). 

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