Halogens iodine atom

The most widely used reactions are those of electrophilic substitution, and under controlled conditions a maximum of three substituting groups, e.g. -NO2 (in the 1,3,5 positions) can be introduced by a nitric acid/sul-phuric acid mixture. Hot cone, sulphuric acid gives sulphonalion whilst halogens and a Lewis acid catalyst allow, e.g., chlorination or brom-ination. Other methods are required for introducing fluorine and iodine atoms. Benzene undergoes the Friedel-Crafts reaction. ... 

The iodine atom in iodobenzene (unlike that in the corresponding aliphatic compounds) is very resistant to the action of alkalis, potassium cyanide, silver nitrite, etc. This firm attachment of the iodine atom to the benzene ring is typical of aromatic halides generally, although in suitably substituted nitio-compounds, such as chloro-2,4-dinitrobenzene, the halogen atom does possess an increased reactivity (p. 262). 

The importance of ozone in the stratosphere has been stressed in Section 9.3.8. The fact that ozone can be decomposed by the halogen monoxides CIO, BrO and 10 means that their presence in the stratosphere contributes to the depletion of the ozone layer. For example, iodine, in the form of methyl iodide, is released into the atmosphere by marine algae and is readily photolysed, by radiation from the sun, to produce iodine atoms which can react with ozone to produce 10 ... 

Iodine reacts with hydrocarbons to form iodine compounds, but compared to the other halogens, the equiUbria are unfavorable because the displacement step with the iodine atom is endothermic, requiring 4066.3 J (971.9 cal) for methane and 799.9 J (191.2 cal) for toluene. Hydrogen iodide can be used to reduce an alkah iodide to hydrocarbon plus molecular iodine. 

In reaction (19) the iodine shown on the left has an oxidation number of zero. After the reaction, some of the iodine atoms have oxidation number +5 and some —1. In other words, the iodine oxidation number has gone both up and down in the reaction. This is an example of selfoxidation-reduction, sometimes called disproportionation. It is a reaction quite typical of, but not at all restricted to, the halogens. 

Fluorine, bromine or iodine atoms can be introduced by treatment of hydroxy- or trialkylsil-oxymetal phthalocyanines with the corresponding halogen acid. 

Finally, a weak jt-type halogen bonding involving a cyclopentadienyl ring and the iodine atom of an iodofluorocarbon [89] is a rare example of a Tt-bonded io do carbon derivative, in contrast to numerous examples of halogen bonding of the latter with n-type electron donors [2,20]. 

The oxidation number of every halogen atom in its compounds is - 1 except for a chlorine, bromine, or iodine atom combined with oxygen or a halogen atom higher in the periodic table. For example, the chlorine atoms in each of the following compounds have oxidation numbers of -1 ... 

Figure 12.5 IODO-GEN is a water-insoluble oxidizing agent that can react with 1251 - to form a highly reactive mixed halogen species, 125IC1. This intermediate can add radioactive iodine atoms to tyrosine or histidine side chain rings.

Because of the size of the iodine atom and the fact that it is easier to oxidize to the +7 state, IF7 is the only XX 7 interhalogen. It is prepared by the reaction of IF5 and F2 at elevated temperatures, and like other halogen fluorides it is a strong fluorinating agent. When it reacts with water, HF and HI04 are produced. 

An alkyl halide (also known as a haloalkane) is an alkane in which one or more hydrogen atoms have been replaced with halogen atoms, such as F, Cl, Br, or I. The functional group of alkyl halides is R—X, where X represents a halogen atom. Alkyl halides are similar in structure, polarity, and reactivity to alcohols. To name an alkyl halide, first name the parent hydrocarbon. Then use the prefix fluoro-, chloro-, bromo-, or iodo-, with a position number, to indicate the presence of a fluorine atom, chlorine atom, bromine atom, or iodine atom. The following Sample Problem shows how to name an alkyl halide. 

Halogenated extinguishing agents are hydrocarbons where one or more hydrogen atom is replaced by fluorine, chlorine, bromine, or iodine atoms. The substituted atom is not only rendered nonflammable, but it acts as a very efficient... 

Since the size of halogen atom Increases as we go down the group in the periodic table, fluorine atom is the smallest and iodine atom, the largest. Consequently the carbon-halogen bond length also Increases from C—to C— I. Some typical bond lengths, bond enthalpies and dipole moments are given in Table 10.2. 

Oxidation of iodoalkanes involves removal of an electron from the halogen nonbonding orbital. The radical-cations of primary and secondary alkyl iodides can be identified in aqueous solution by their absorption spectra and have half-lives of microseconds [1]. They are formed during pulse radiolysis of the iodoalkane in aqueous solution in the presence of nitrous oxide. This system generates hydroxyl radicals, which remove an electron from the iodine atom lone pair. Iodoalkane radical-anions complex with the lone-pair on other heteroatoms to form a lollo three-electron bond. In aqueous solution, the radical-cation of iodomethane is involved in an equlibrium indicated by Equation 2.1. 

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