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e nitro derivatives of the hydrocarbons of the benzene series is very simple. It is only necessary to bring the hydrocarbon into contact with strong nitric acid, when the reaction takes place, and one or more of the hydrogen atoms of the hydrocarbon are replaced by the nitryl group (NO_{2}). Thus by the action of nitric acid on benzene (or benzol), mono-nitro-benzene is formed:-- C_{6}H_{6} + HNO_{3} = C_{6}H_{5}.NO_{2} +H_{2}O. Mono-nitro-benzene. By the action of another molecule of nitric acid, the di-nitro-benzene is formed:-- C_{6}H_{5}.NO_{2} + HNO_{3} = C_{6}H_{4}(NO_{2})_{2} + H_{2}O. Di-nitro-benzene. These nitro bodies are not acids, nor are they ethereal salts of nitrous acid, as nitro-glycerine is of glycerine. They are regarded as formed from nitric acid by the replacement of hydroxyl by benzene radicals. ~Mono-nitro Benzene~ is made by treating benzene with concentrated nitric acid, or a mixture of nitric and sulphuric acids. The latter, as in the case of the nitration of glycerine, takes no part in the reaction, but only prevents the dilution of the nitric acid by the water formed in the reaction. Small quantities may be made thus:--Take 150 c.c. of H_{2}SO_{4} and 75 c.c. HNO_{3}, or 1 part nitric to 2 parts sulphuric acid, and put in a beaker standing in cold water; then add 15 to 20 c.c. of benzene, drop by drop, waiting between each addition for the completion of the reaction, and shake well during the operation. When finished, pour contents of beaker into about a litre of cold water; the nitro-benzol will sink to the bottom. Decant the water, and wash the nitro-benzol two or three times in a separating funnel with water. Finally, dry the product by adding a little granulated calcium chloride, and allowing to stand for some little time, it may then be distilled. Nitro-benzene is a heavy oily liquid which boils at 205 deg. C., has a specific gravity of 1.2, and an odour like that of oil of bitter almonds. In the arts it is chiefly used in the preparation of aniline. ~Di-nitro Benzene~ is a product of the further action of nitric acid on benzene or nitro-benzene. It crystallises in long fine needles or thin rhombic plates, and melts at 89.9 deg. C. It can be made thus:--The acid mixture used consists of equal parts of nitric and sulphuric acids, say 50 c.c. of each, and without cooling add very slowly 10 c.c. of benzene from a pipette. A
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