Sulphuric acid sulphur

The aqueous solutions decompose slowly at ordinary temperatures, depositing sulphur, sulphuric acid being formed in solution. At 160° C. the decomposition is rapid.1... 

Numerous processes have been developed for combined desulphurisation and denitrification of the flue gases. Most processes are still at the laboratory scale and there are very few plants operating at full commercial scale. Most combined processes are considered to be complex and expensive. That opinion may change, however, as more stringent standards are introduced for both sulphur and nitrogen oxide emissions together with restrictions on residue disposal. Many combined processes produce a refined by-product, (eg sulphur, sulphuric acid). 

Colourless, volatile liquid with a strong pearlike odour, b.p. 138-5 C. Manufactured by heating amyl alcohol (1-pentanol) with potassium ethanoate and sulphuric acid or by heating amyl alcohol with ethyl ethanoate in the presence of a little sulphuric acid. Commercial... 

On acetylation it gives acetanilide. Nitrated with some decomposition to a mixture of 2-and 4-nitroanilines. It is basic and gives water-soluble salts with mineral acids. Heating aniline sulphate at 190 C gives sulphanilic add. When heated with alkyl chlorides or aliphatic alcohols mono- and di-alkyl derivatives are obtained, e.g. dimethylaniline. Treatment with trichloroethylene gives phenylglycine. With glycerol and sulphuric acid (Skraup s reaction) quinoline is obtained, while quinaldine can be prepared by the reaction between aniline, paraldehyde and hydrochloric acid. 

It is prepared by acidifying an alkali solution of anthrone or by reduction of anthraquinone with aluminium powder and concentrated sulphuric acid. 

It is used in the preparation of benzanthrone by heating with glycerol and sulphuric acid (Skraup s reaction). 

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. ... 

Prepared by the sulphonation of benzene in the liquid state or by passing benzene vapour into concentrated sulphuric acid at 150-180"C. 

Isobutyl alcohol, isobutanol, 2-methyl-propanol, isopropyl carbinol, Me2CHCH20H. B.p. 108°C. Occurs in fusel-oil. Oxidized by potassium permanganate to 2-methyl-propanoic acid dehydrated by strong sulphuric acid to 2-methylpropene. 

Tertiary butyl alcohol, trimethyl carbinol, tertiary butanol. 2-methyl-2-propanol, Me3COH. Colourless prisms, m.p. 25°C, b.p. 83°C. Prepared by absorbing isobutene (2-methylpropene) in sulphuric acid, neutralizing and steam distilling the liquor. Converted to isobutene by heating with oxalic acid. Potassium-/-buloxide is a very strong base. 

Buiene, -butylene, CH3CH CHCH3-Prepared by heating 2-buianol with sulphuric acid. It occurs as two geometrical isomers. 

Secondary butyl ethanoale, CH3CHaCH(Me)0-0CCH3, b.p. 112-113°C. Manufactured by heating 2-butene with etha-noic and sulphuric acids in water. 

With dilute sulphuric acid citral forms p-cymene. Citral can be condensed with propa-none to form a ketone, pseudoionone, C13H20O, which is technically important, as it is readily convertible into a and -ionone. 

COT is prepared by the polymerization of ethyne at moderate temperature and pressure in the presence of nickel salts. The molecule is non-planar and behaves as a typical cyclic olefin, having no aromatic properties. It may be catalytically hydrogenated to cyclo-octene, but with Zn and dil. sulphuric acid gives 1,3,6-cyclooclairiene. It reacts with maleic anhydride to give an adduct, m.p. 166 C, derived from the isomeric structure bicyclo-4,2,0-octa-2,4,7-triene(I) ... 

M.p. I08-5 C. Ordinary DDT contains about 15% of the 2,4 -isomer, and is prepared from chloral, chlorobenzene and sulphuric acid. It is non-phytotoxic to most plants. It is a powerful and persistent insecticide, used most effectively to control mosquitoes in countries where malaria is a problem. It is stored in the bodies of animals and birds. 

Dehumidification may be effected by cooling. Where small quantities of dry air are required dehumidification can be carried out using chemical absorbents, e.g. calcium chloride, phosphorus pentoxide, sulphuric acid, etc. 

The sodium salts of sulphuric acid esters of dextran are used as anticoagulants for the same purposes as heparin. 

Diamond is very resistant to chemical reagents potassium dichromate and sulphuric acid attack it with the formation of CO2. It burns in air or oxygen at 700 C to CO2 leaving scarcely any ash some forms of bort may leave as much as 4-5% ash. 

HOCHj CHjOH. Colourless, odourless, rather viscous hygroscopic liquid having a sweet taste, b.p. 197 C. Manufactured from ethylene chlorohydrin and NaHC03 solution, or by the hydration of ethylene oxide with dilute sulphuric acid or water under pressure at 195°C. Used in anti-freezes and coolants for engines (50 %) and in manufacture of polyester fibres (e.g. Terylene) and in the manufacture of various esters used as plasticizers. U.S. production 1979 1 900 000 tonnes. 

Prepared by heating aniline with methanol and a little sulphuric acid at 2I5 C. 

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