Halides name , bromides . chlorides

Foster and Wolfrom, in 1956, encountered an anomalous reaction of methyl 3,4-0-isopropylidene-2-0-(sodium thiolthiocarbonyl)- S-D-arabino-pyranoside (LIX) with certain alkyl halides, namely ethyl iodide, propyl bromide, isopropyl bromide, and ter<-butyl chloride. The expected 2-0-[(alkylthio)thiocarbonyl] esters LX were not formed, but, in each case, bis(methyl 3,4-0-isopropylidene-j8-D-arabinopyranoside) 2-thionocarbonate (VI) was isolated. A probable explanation of this behavior was suggested... 

Acyl halides are compounds that have a halogen atom in place of the OH group of a carboxylic acid. The most common acyl halides are acyl chlorides and acyl bromides. Acyl halides are named by using the acid name and replacing ic acid with yl chloride (or yl bromide ). For acids ending with carboxylic acid, carboxylic acid is replaced with carbonyl chloride (or bromide ). 

The lUPAC rules permit alkyl halides to be named m two different ways called func twnal class nomenclature and substitutive nomenclature In functional class nomencla ture the alkyl group and the halide (fluoride chloride bromide or iodide) are desig nated as separate words The alkyl group is named on the basis of its longest continuous chain beginning at the carbon to which the halogen is attached... 

It is known that the order of acidity of hydrogen halides (HX, where X = F, Cl, Br, I) in the gas phase can be successfully predicted by quantum chemical considerations, namely, F < Cl < Br < I. However, in aqueous solution, whereas hydrogen chloride, bromide, and iodide completely dissociate in aqueous solutions, hydrogen fluoride shows a small dissociation constant. This phenomenon is explained by studying free energy changes associated with the chemical equilibrium HX + H2O + HjO in the solu-... 

Monatomic anions, such as the Cl- ions in sodium chloride and the O2- ions in quicklime (CaO), are named by adding the suffix -ide and the word ion to the first part of the name of the element (the stem" of its name), as shown in Table D.l thus, S2 is a sulfide ion and O2 is an oxide ion. There is usually no need to specify the charge, because most elements that form monatomic anions form only one kind of ion. The ions formed by the halogens are collectively called halide ions and include fluoride (F ), chloride (Cl-), bromide (Br-), and iodide (I ) ions. 

In general, the halide ions, namely chloride, bromide and iodide are very weakly basic in character so much so that they cannot react quantitatively with acetous perchloric acid. In order to overcome this problem, mercuric acetate is usually added (it remains undissociated in acetic acid solution) to a halide salt thereby causing the replacement of halide ion by an equivalent amount of acetate ion, which serves as a strong base in acetic acid as shown below ... 

The use of mixtures of sodium hydroxide and benzyltrimethylammonium chloride or tetrabutylammonium bromide failed to enhance the DPGE alkylation of HEC by the in situ formation of the corresponding quaternary ammonium hydroxide phase transfer catalyst. These quaternary ammonium halides are too soluble in aqueous /-butyl alcohol and are preferentially extracted into the organic phase. Mixtures of benzyltrimethylammonium hydroxide and sodium acetate were also ineffective in enhancing the DPGE alkylation of HEC for the same reason, namely preferential solubility of benzyltrimethylammonium acetate in the organic phase. 

The haloperoxidases are a class of enzymes that catalyze the oxidation of halides via a reactive peroxometal active site. These enzymes are named according to the most electronegative halide they are able to oxidize. Hence, a bromoperoxidase can oxidize bromide and iodide but not chloride, whereas a chloroperoxidase can oxidize all three. Haloperoxidases are found in most living organisms and predominately fall into two classes the iron heme-based and vanadium-dependent enzymes. Of these, heme-based enzymes are found in mammals, where they provide a vital... 

Primary and secondary alkyl bromides, iodides, and sulfonates can be reduced to the corresponding alkanes with LiBHEt3 (superhydride) or with lithium aluminum hydride (LiAlH4, other names lithium tetrahydridoaluminate or lithium alanate). If such a reaction occurs at a stereocenter, the reaction proceeds with substantial or often even complete stereoselectivity via backside attack by the hydride transfer reagent. The reduction of alkyl chlorides to alkanes is much easier with superhydride than with LiAlH4. The same is true for sterically hindered halides and sulfonates ... 

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