Chem group project the Haloalkanes

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1 Chem group project the Haloalkanes The haloalkanes (also known as halogenoalkanes) are a group of chemical compounds derived from alkanes containing one or more halogens. They are the general class of halocarbons, although the distinction is not often made. Haloalkanes are widely used commercially and are known under many chemical and commercial names. They are used as flame retardants, fire extinguishants, refrigerants, propellants, solvents. Many halocarbons have also been shown to be serious pollutants and toxins. For example, the chlorofluorocarbons have been shown to lead to ozone depletion. Methyl iodide, a naturally occurring substance, however, does not have ozone-depleting properties and the United States Environmental Protection Agency has designated the compound a non-ozone layer depleter. Haloalkanes have been known for centuries. Especially included the addition of halogens to alkenes, hydrohalogenation of alkenes, and the conversion of alcohols to alkyl halides. These methods are so reliable and so easily implemented that haloalkanes became cheaply available for use in industrial chemistry because the halide could be further replaced by other functional groups. While most haloalkanes are human-produced, non-artificial-source haloalkanes do occur on Earth. More than 1600 halogenated organics have been identified, with bromoalkanes being the most common haloalkanes. Halogenated alkanes in land plants are more rare, but do occur, as for example the fluoroacetate produced as a toxin by at least 40 species of known plants. Classes of haloalkanes From the structural perspective, haloalkanes can be classified according to the connectivity of the carbon atom to which the halogen is attached. In primary haloalkanes, the carbon that carries the halogen atom is only attached to one other alkyl group. An example is chloroethane (CH 3 CH 2 Cl). In secondary (2 ) haloalkanes, the carbon that carries the halogen atom has two C C bonds. In tertiary (3 ) haloalkanes, the carbon that carries the halogen atom has three C C bonds. Haloalkanes can also be classified according to the type of halogen. Haloalkanes containing carbon bonded to fluorine, chlorine, bromine, and iodine results in organofluorine, organochlorine, organobromine and organoiodine compounds, respectively. Compounds containing more than one kind of halogen are also possible.

2 Properties Haloalkanes generally resemble the parent alkanes in being colorless, relatively odorless, and hydrophobic. Their boiling points are higher than the corresponding alkanes and scale with the atomic weight and number of halides. This is due to the increased strength of the intermolecular forces from London dispersion to dipole-dipole interaction because of the increased polarity. Thus carbon tetraiodide (CI 4 ) is a solid whereas carbon tetrafluoride (CF 4 ) is a gas. As they contain fewer C H bonds, halocarbons are less flammable than alkanes, and some are used in fire extinguishers. Haloalkanes are better solvents than the corresponding alkanes because of their increased polarity. Haloalkanes containing halogens other than fluorine are more reactive than the parent alkanes it is this reactivity that is the basis of most controversies. Occurrence Haloalkanes are of wide interest because they are widespread and have diverse beneficial and detrimental impacts => The oceans are estimated to release 1-2 million tons of bromomethane annually. A large number of pharmaceuticals contain halogens, especially fluorine. An estimated one fifth of pharmaceuticals contain fluorine, including several of the top drugs. Include 5-fluorouracil, fluoxetine (Prozac), paroxetine (Paxil), ciprofloxacin (Cipro), mefloquine, andfluconazole. The beneficial effects arise because the C-F bond is relatively unreactive. Fluorine-substituted ethers are volatile anesthetics, including the commercial products methoxyflurane, enflurane, isoflurane, sevoflurane and desflurane. Fluorocarbon anesthetics reduce the hazard of flammability with diethyl ether and cyclopropane. Perfluorinated alkanes are used as blood substitutes. Teflon structure

3 Chlorinated or fluorinated alkenes undergo polymerization. Important halogenated polymers include polyvinyl chloride (PVC), and polytetrafluoroethene (PTFE, or Teflon). The production of these materials releases substantial amounts of wastes. IUPAC The formal naming of haloalkanes should follow IUPAC nomenclature, which put the halogen as a prefix to the alkane. Example- ethane with bromine becomes bromoethane, methane with four chlorine groups becomes tetrachloromethane. However, many of these compounds have already an established trivial name, which is endorsed by the IUPAC nomenclature, for example chloroform(trichloromethane) and methylene chloride (dichloromethane). For unambiguity, this article follows the systematic naming scheme throughout. From alkanes Alkanes react with halogens by free radical halogenation. In this reaction a hydrogen atom is removed from the alkane, then replaced by a halogen atom by reaction with a diatomic halogen molecule. The reactive intermediate in this reaction is a free radical and the reaction is called a radical chain reaction. Free radical halogenation typically produces a mixture of compounds mono- or multihalogenated at various positions. It is possible to predict the results of a halogenation reaction based on bond dissociation energies and the relative stabilities of the radical intermediates. Another factor to consider is the probability of reaction at each carbon atom, from a statistical point of view. Due to the different dipole moments of the product mixture, it may be possible to separate them by distillation. From alkenes and alkynes In hydrohalogenation, an alkene reacts with a dry hydrogen halide (HX) like hydrogen chloride (HCl) or hydrogen bromide (HBr) to form a mono-haloalkane. The double bond of the alkene is replaced by two new bonds, one with the halogen and one with the hydrogen atom of the hydrohalic acid. Markovnikov's rule states that in this reaction, the halogen is more likely to become attached to the more substituted carbon. This is a electrophilic addition reaction. Water must be absent otherwise there will be a side product of a halohydrin. The reaction is necessarily to be carried out in a dry inert solvent such as CCl 4 or directly in the gaseous phase.

4 Alkenes also react with halogens (X 2 ) to form haloalkanes with two neighboring halogen atoms in a halogen addition reaction. Alkynes react similarly, forming the tetrahalo compounds. This is sometimes known as "decolorizing" the halogen, since the reagent X 2 is colored and the product is usually colorless. From alcohols Tertiary alkanol reacts with hydrochloric acid directly to produce tertiary chloroalkane, but if primary or secondary alkanol is used, an activator such as zinc chloride is needed. This reaction is exploited in the Lucas test. The most popular conversion is effected by reacting the alcohol with thionyl chloride (SOCl 2 ) in the "Darzen's Process," which is one of the most convenient laboratory methods because the byproducts are gaseous. Both phosphorus pentachloride (PCl 5 ) and phosphorus trichloride(pcl 3 ) also convert the hydroxyl group to the chloride. Alcohols may likewise be converted to bromoalkanes using hydrobromic acid or phosphorus tribromide (PBr 3 ). A catalytic amount of PBr 3 may be used for the transformation using phosphorus and bromine; PBr 3 is formed in situ. Iodoalkanes may similarly be prepared using using red phosphorus and iodine (equivalent to phosphorus triiodide). The Appel reaction is also useful for preparing alkyl halides. The reagent is tetrahalomethane and triphenylphosphine; the co-products are haloform andtriphenylphosphine oxide. From carboxylic acids Two methods for the synthesis of alkyl halides from carboxylic acids are the Hunsdiecker reaction and the Kochi reaction. Biosynthesis Many chloro and bromolkanes are formed naturally. The principal pathways involve the enzymes chloroperoxidase and bromoperoxidase. Reactions Haloalkanes are reactive towards nucleophiles. They are polar molecules: the carbon to which the halogen is attached is slightly electropositive where the halogen is

5 slightly electronegative. This results in an electron deficient (electrophilic) carbon which, inevitably, attracts nucleophiles. Substitution Substitution reactions involve the replacement of the halogen with another molecule thus leaving saturated hydrocarbons, as well as the halogenated product. Alkyl halides behave as the R + synthon, and readily react with nucleophiles. Hydrolysis, a reaction in which water breaks a bond, is a good example of the nucleophilic nature of halogenoalkanes. The polar bond attracts a hydroxide ion, OH (NaOH (aq) being a common source of this ion). This OH is a nucleophile with a clearly negative charge, as it has excess electrons it donates them to the carbon, which results in a covalent bond between the two. Thus C X is broken by heterolytic fission resulting in a halide ion, X. As can be seen, the OH is now attached to the alkyl group, creating an alcohol. (Hydrolysis of bromoethane, for example, yields ethanol). Reaction with ammonia give primary amines. Alkyl chlorides and bromides are readily substituted by iodide in the Finkelstein reaction. The alkyl iodides produced easily undergo further reaction. Sodium iodide is used thus as a catalyst. Alkyl halides react with ionic nucleophiles (e.g. cyanide, thiocyanate, azide); the halogen is replaced by the respective group. This is of great synthetic utility: alkyl chlorides are often inexpensively available. For example, after undergoing substitution reactions, alkyl cyanides may be hydrolyzed to carboxylic acids, or reduced to primary amines using lithium aluminium hydride. Alkyl azides may be reduced to primary alkyl amines by the Staudinger reduction or lithium aluminium hydride. Amines may also be prepared from alkyl halides in amine alkylation, thegabriel synthesis and Delepine reaction, by undergoing nucleophilic substitution with potassium phthalimide or hexamine respectively, followed by hydrolysis. In the presence of a base, alkyl halides alkylate alcohols, amines, and thiols to obtain ethers, N-substituted amines, and thioethers respectively. They are substituted by Grignard reagents to give magnesium salts and an extended alkyl compound. Mechanism Where the rate-determining step of a nucleophilic substitution reaction is unimolecular, it is known as an S N 1 reaction. In this case, the slowest (thus rate-determining step) is the heterolysis of a carbon-halogen bond to give a

6 carbocation and the halide anion. The nucleophile (electron donor) attacks the carbocation to give the product. S N 1 reactions are associated with the racemization of the compound, as the trigonal planar carbocation may be attacked from either face. They are favored mechanism for tertiary alkyl halides, due to the stabilization of the positive charge on the carbocation by three electron-donating alkyl groups. They are also preferred where the substituents are sterically bulky, hindering the S N 2 mechanism. Applications Haloalkanes are widely used as synthon equivalents to alkyl cation (R+) in organic synthesis. They can also participate in a wide variety of other organic reactions. Short chain haloalkanes such as dichloromethane, trichloromethane (chloroform) and tetrachloromethane are commonly used as hydrophobic solvents in chemistry. They were formerly very common in industry, however, their use has been greatly curtailed due to their toxicity and negative environmental effects. Chlorofluorocarbons were used almost universally as refrigerants and propellants due to their relatively low toxicity and high heat of vaporization. Starting in the 1980s, as their contribution to ozone depletion became known, their use was increasingly restricted, and they have now largely been replaced by HFCs. 5E(39) 5E(43) Tong Yuk Choi Wong Siu Man 5E(25) Chan Chun Chung 5E(33) Law Chung Kwong