This section is from the book "Encyclopedia Of Diet. A Treatise on the Food Question", by Eugene Christian. Also available from Amazon: Encyclopedia of Diet.
Only a few of the most important groups of the organic or life-formed carbon compounds will be considered in this work, namely: a Hydrocarbons b Alcohols c Glycerin d Aldehydes and ethers.
e Organic acids f Carbohydrates g Fats.
Hydrocarbons are compounds of the two elements carbon and hydrogen. These compounds are very important in industrial chemistry. They are found in petroleum, coal-tar, etc., which were originally formed from decaying and petrifying masses of plants. Gasoline, benzin, naphtha, acetylene, methane, etc., are some of the industrial forms by which hydrocarbons are known in commerce.
Uses of hydrocarbons in industrial chemistry.
The industries based upon the chemistry of these hydrocarbons are very complex and interesting. Coal-tar yields, by repeated distillation and chemical reaction, thousands of compounds, many of which find important industrial usages. Coal-tar dyes are very numerous and of wonderful coloring power. They have been extensively used in the artificial coloring of manufactured foods. The Federal Pure Food Law attempted to prohibit this. In fact, it was the pernicious effect and extensive use of these poisons that stimulated the passage of the "Food and Drugs Act." Another interesting product of the coal-tar industry is saccharin. Saccharin has no food value whatever, but it is 280 times sweeter than cane-sugar, and is therefore used as a substitute in sweetening some prepared foods.
Coal-tar products.
To the ordinary mind the term alcohol refers only to the intoxicating element in liquors. To the chemist, alcohol has a much broader significance. There are many varieties of alcohols, of which ethyl alcohol (C2H5.HO), which is found in liquors, is only one example. Another form of alcohol which is fairly well known is wood or methyl alcohol (CH3.OH).
There are also higher alcohols, that is, those having more complex chemical formulas, such as butyl alcohol. In the fermentation of grains or fruits for intoxicating Jiquors, a small quantity of the various higher alcohols is formed. These higher alcohols are more intoxicating and more harmful to the human system than ethyl alcohol, and must be separated from the latter by careful distillation. The poisonous property of green whisky and cheap liquors is generally due to the presence of higher alcohols.
Varieties of alcohol.
Formation of higher alcohols.
Alcohol does not exist in normal, fresh plant or animal substances except in very minute quantities. It is formed from sugar by fermentation. This fermentation is due to a microscopic yeast-plant.
Another form of alcohol is glycerin (C3H803). It is of special interest to the food chemist because it enters into the formation of all fats..
These are compounds containing carbon, hydrogen, and oxygen, and are closely related to alcohols. In fact, they are formed from alcohols by a process of oxidation, hence contain a little larger proportion of oxygen than the related alcohol.
An example of aldehyde with which many are familiar is formaldehyde, which is used in laboratories for the preservation of animal-tissues for dissection. This formaldehyde is a very strong germicide; that is, it is poisonous to bacteria or germs. For this reason it is used as a preservative of milk, a use which is forbidden by the "Food and Drugs Act," because formaldehyde is also poisonous to the human system.
Ethyl ether, which is used as an anesthetic or to produce insensibility to pain, will serve as an illustration of this group of compounds. When analyzing foods in chemical laboratories, ether is commonly used for dissolving fats.
How formed.
Uses of formaldehyde.
Uses of ether
It will be remembered that acids were studied in the second lesson. It was found that the common properties of acids are a sour taste, ability to combine with alkalis in the formation of salts, and that all acids contain hydrogen. These same properties that were studied in the second lesson in reference to mineral acids, such as hydrochloric and sulfuric, apply also to the organic acids. The organic acids, however, as a class are not so strong or active as the mineral acids.
All organic acids are compounds of carbon, hydrogen, and oxygen, the same as alcohols and ethers, the chief difference between these compounds and acids being that the acids contain a greater proportion of oxygen. One of the simplest organic acids is formic acid (HCO.OH). This acid is the active principle in the sting of the red ant, and also of stinging nettles. It produces blisters when applied to the skin.
Properties of organic acids.
Impure acetic acid (C2H402) is very well known to all under the name of vinegar. Acetic acid may be obtained by distilling wood. If it could be manufactured cheaply enough, vinegar made from wood would be fully as wholesome as the best cider vinegars, but this being an expensive process of manufacture, the temptation of the food adulterator is to make the vinegar of sulfuric acid, which is much cheaper than the mild acetic acid, but much more harmful when taken into the body.
The formic and the acetic acids are examples of a series of organic acids known as fatty acids. Other members of the series are -
Process of making acetic acid.
Propionic acid......C3H602
Butyric " ......C4H802
Palmitic " ......C16H3202
Stearic " ......C18H3602
These fatty acids are very important to the food scientist as they combine with glycerin to form fats. When combined with alkalis under a certain temperature they form soap. Perhaps some of our older students may remember the soap kettle on the farm at home, in which lard cracklings and other fatty fragments of the animal were boiled with lye or caustic potash to form home-made soap. The chemical action that took place was a combination of these fatty acids with the caustic potash or lye. The glycerin was set free and remained in the bottom of the kettle as soft soap. Reference will be made to these acids again, in Lesson IV (Chemistry Of Foods), where the study of fats will be taken up in detail. (See "Fats and Oils," under Lesson IV, Chemistry of Foods, p. 122).
Process of making soap.
There are some other forms of organic acids which do not belong in the fatty series; that is, they do not contain the same general proportions of carbon and hydrogen. One of these is oxalic acid (C2H2O4) which is found in certain plants, such as sorrel, and is an active poison. Oxalic acid is used in the household for taking iron-rust out of cloth.
Lactic acid (C3H603) is the acid of sour milk. Malic acid (C4H605) is found in many fruits, such as apples, apricots, currants, pears, plums, prunes, etc. Tartaric acid (C4H606) is found principally in grapes. It is one of the constituent elements in the sediment found in wine casks, and is the active principle in cream of tartar. The latter is a potassium salt of tartaric acid.
Oxalic Acid.
Lactic, malic and tartaric acids.
Citric acid (C6H807) is one of the most important of the organic acids from the standpoint of the food chemist. It is the active principle of citrus-fruits, such as grape-fruit, lemons, limes, oranges, etc. Lemons contain as high as five per cent of this acid. Citric acid is often used to make lemonade, and if pure citric acid is used, the manufactured product is equal to the original, except from a sentimental standpoint of having the genuine. The danger is, as in the case of adulterated vinegar, that the manufacturer may be tempted to use cheaper mineral acids instead of citric acid.
The other above-named groups of organic compounds which are formed from the three elements carbon, hydrogen, and oxygen - (f) carbohydrates and (g) fats - are very important to the food chemist. These will be considered in detail in Lesson IV (Chemistry Of Foods). See pages 107-125.
Citric acid.
 
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