Molecules carbon-containing

In the free state, carbon molecules containing less than 60 carbon atoms are generally unstable, although many smaller ones have been... 

Virtually all the complex lipids are fatty acid derivatives, and in most cases they are covalently linked to an alcohol. One of the most common alcohols found in human metabolism is glycerol, a three-carbon molecule containing three hydroxyl groups. 

Hydrocarbons constitute the essential components of petroleum their molecules contain only carbon and hydrogen they are grouped into many chemical families according to their structure. All structures are based on the quadrivalency of carbon. 

A similar situation holds foi a molecule containing a tetrahedral carbon is shown in (Figure 16). The reaction converting one enantiomer to another, is formally equivalent to the exchange of two sigma-bond electr on pair s, and... 

If an open-chain organic molecule contains an electron acceptor and an electron donor site, two carbon atoms may be combined intramolecularly. This corresponds to the synthesis of a monocyclic compound. 

Section 7 2 The most common kind of chiral molecule contains a carbon atom that bears four different atoms or groups Such an atom is called a chirality center Table 7 2 shows the enantiomers of 2 chlorobutane C 2 is a chi rahty center m 2 chlorobutane... 

Index of hydrogen deficiency (Section 13 23) A measure of the total double bonds and nngs a molecule contains It is determined by comparing the molecular formula C Hj. of the compound to that of an alkane that has the same number of carbons according to the equation... 

A simpler representation of molecules containing asymmetric carbon atoms is the Fischer projection, which is shown here for the same lactic acid configurations. A Fischer projection involves... 

Some heteronuclear diatomic molecules, such as nitric oxide (NO), carbon monoxide (CO) and the short-lived CN molecule, contain atoms which are sufficiently similar that the MOs resemble quite closely those of homonuclear diatomics. In nitric oxide the 15 electrons can be fed into MOs, in the order relevant to O2 and F2, to give the ground configuration... 

Chiral separations are concerned with separating molecules that can exist as nonsupetimposable mirror images. Examples of these types of molecules, called enantiomers or optical isomers are illustrated in Figure 1. Although chirahty is often associated with compounds containing a tetrahedral carbon with four different substituents, other atoms, such as phosphoms or sulfur, may also be chiral. In addition, molecules containing a center of asymmetry, such as hexahehcene, tetrasubstituted adamantanes, and substituted aHenes or molecules with hindered rotation, such as some 2,2 disubstituted binaphthyls, may also be chiral. Compounds exhibiting a center of asymmetry are called atropisomers. An extensive review of stereochemistry may be found under Pharmaceuticals, Chiral. 

Two of the perfluoropolyether fluid stmctures yet to be commercialized are interesting. The first stmcture is a strictly alternating copolymer of ethylene oxide and methylene oxide, which has the longest Hquid range of any molecule containing carbon (40). The second stmcture is the perfluoromethylene oxide polyether which has low temperature Hquid properties down to —120° C ... 

Carboxylate soaps are most commonly formed through either direct or indirect reaction of aqueous caustic soda, ie, alkaH earth metal hydroxides such as NaOH, with fats and oils from natural sources, ie, triglycerides. Fats and oils are typically composed of both saturated and unsaturated fatty acid molecules containing between 8 and 20 carbons randomly linked through ester bonds to a glycerol [56-81-5] backbone. Overall, the reaction of caustic with triglyceride yields glycerol (qv) and soap in a reaction known as saponification. The reaction is shown in equation 1. 

With Unsaturated Compounds. The reaction of unsaturated organic compounds with carbon monoxide and molecules containing an active hydrogen atom leads to a variety of interesting organic products. The hydroformylation reaction is the most important member of this class of reactions. When the hydroformylation reaction of ethylene takes place in an aqueous medium, diethyl ketone [96-22-0] is obtained as the principal product instead of propionaldehyde [123-38-6] (59). Ethylene, carbon monoxide, and water also yield propionic acid [79-09-4] under mild conditions (448—468 K and 3—7 MPa or 30—70 atm) using cobalt or rhodium catalysts containing bromide or iodide (60,61). 

If a molecule contains several asymmetric C atoms, then the diastereomers show diastereotopic shifts. Clionasterol (28a) and sitosterol (28b) for example, are two steroids that differ only in the absolute configuration at one carbon atom, C-24 Differing shifts of C nuclei close to this asymmetric C atom in 28a and b identify the two diastereomers including the absolute configuration of C-24 in both. The absolute configurations of carboxylic acids in pyrrolizidine ester alkaloids are also reflected in diastereotopic H and C shifts which is used in solving problem 54. 

The C50 molecule contains 12 pentagons and 20 hexagons. This type of hexagonal-pentagonal structure closely resembles the geodesic domes developed by the architect and engineer R. Buckminster Fuller, after whom the molecule is named. In the Csn molecule each carbon atom is bonded to three... 

Similarly, the two faces at a trigonal earbon in a molecule containing a stereogenic center are diastereotopie. Both ehiral and achiral reactants can distinguish between these diastereotopie faces. Many examples of diastereotopie transformations of sueh eompounds are known. One of the cases that has been examined elosely is addition reactions at a trigonal center adjacent to an asymmetric carbon. Particular attention has been given to the case of nucleophilie addition to carbonyl groups. 

Amines, like ammonia NH3, are polar compounds and, except for tertiary amines, form intermolecular hydrogen bonds leading to higher boiling points than non-polar compounds of the same molecular weight, but lower boiling points than alcohols or acids. The smaller molecules, containing up to about six carbon atoms, dissolve in water. Aliphatic amines are similar in basicity to ammonia and form water-soluble salts with acids ... 

Primary alkyl chlorides are fairly stable to fluorine displacement. When fluorinated, 1-chloropropane is converted to 1-chloroheptafluoropropane and 1-chloto-2-methylbutane produces 39% l-chlorononafluoro-2-methylbutane and 19% perfluoro-2-methylbutane. Secondary and tertiary alkyl chlorides can undergo 1,2-chlorine shifts to afford perfluonnated primary alkyl chlorides 2-Chloro-2-methylpropane gives l-chlorononafluoro-2-methylpropane, and three products are obtained by the fluorination of 3-chloropentane [7] (equation 1). Aerosol fluorina-tion of dichloromethane produces dichlorodifluoromethane which is isolated in 98% purity [4 (equation 2). If the molecule contains only carbon and halogens, the picture is different. Molecular beam analysis has shown that the reaction of fluorine with carbon tetrachlonde, lodotrichloromethane, or bromotrichloromethane proceeds first by abstraction of halogen to form a trichloromethyl radical [5]... 

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