спирть

or more groups-HE, with the hydroxyl group linked to an

aliphatic carbon atom (compounds in which the carbon atom in the group WITH-IT is part of the aromatic nucleus, are called phenols)

the structure taken as a basis
1. Depending on the number

of hydroxyl groups in the molecule, alcohols are divided into: a) monatomic (consist of a single hydroxyl IT group), for example, methanol CH3OH, ethanol SON, propane SON b) polyatomic (two or more hydroxyl groups), for example, ethylene glycol HO-CH2-CH2-OH, glycerin HO-CH2-CH(Oh)-CH2-OH, pentaerythritol C(SNON)4.

in most cases, unstable and easily converted into aldehydes, replay

with water: RCH(OH)2 ® RCH=O + H2O
Alcohols containing three groups HE has one carbon atom , do not exist.

the group HE, alcohols are divided into: (a) primary, which group

is linked to a primary carbon atom. The primary is called the carbon atom (red) is associated with only one carbon atom. Examples of primary alcohols - ethanol CH3-CH2-OH, propane CH3-CH2-CH2-OH. b) secondary, which group is linked to a secondary carbon atom. The secondary carbon atom (highlighted in blue) is associated simultaneously with two carbon atoms, for example, secondary propel alcohol, secondary butane (Fig. 1).

Fig. 1. THE STRUCTURE OF SECONDARY ALCOHOLS

is linked to tertiary carbon atom. Tertiary carbon atom (highlighted

in green) is associated simultaneously with three neighboring carbon atoms, for example, tertiary butane and pentane (Fig. 2).

HE is in the group, the alcohols are divided into

marginal (methanol, ethanol, propane), unsaturated, for example, ally alcohol CH2=CH-CH2 -, HE, aromatic (e.g., benzyl alcohol SNNAN) containing the group R is an aromatic group. Unsaturated alcohols, for whom HE is the group adjacent to the double bond, i.e. linked to the carbon atom participating simultaneously in the formation of double bond (e.g., vinyl alcohol CH2=CH-OH), a highly unstable and immediately are isomerizes (see ISOMERIZATION) to aldehydes or ketenes:CH2=CH–OH ® CH3–CH=O

nomenclature: the name of the organic group is converted to

an adjective (with the help of the suffix and the end of the "new" and add the word "alcohol":

СН3ОН methyl alcohol

С2Н5ОН ethyl alcohol

(Н3С)2СНОН isopropyl alcohol

С4Н9ОН butyl alcohol

is more complex, use all organic chemistry rules. Names, made

in such rules, called systematic. In accordance with these rules, the hydrocarbon chain is numbered from the end nearer HE is group. Then use this numbering to indicate the position of different substituent's in the main chain, at the end of the title add the suffix "old" and a number, indicating the position of Oh groups (Fig. 4):

Fig. 4. SYSTEMATIC NAMES OF ALCOHOLS

indices of selected distinct colors. Systematic names of the simplest alcohols

are by the same rules: methanol, ethanol, butane. For some spirits remained trivial (simplified) names, historically: property alcohol NCS-CH2 -, HE, glycerin HO-CH2-CH(Oh)-CH2-OH, pentaerythritol C(SNO)4, finitely alcohol SN-CH2-CH2-OH.

the first three of the simplest representative - methanol, ethanol

and propane, and tertiary butane (NS)SON - mixed with water in any ratio. When the number of atoms in the organic group is beginning to affect hydrophobic (water-repellent) effect, the solubility in water becomes limited, and in the case of R containing more than 9 carbon atoms, practically disappears. Due to the presence of Oh groups between molecules of alcohols hydrogen bonds occur. The result of all alcohols higher boiling point than the corresponding hydrocarbons, for example, Kip. ethanol +78° C, and T. Kip. ethane -88,63° C; b. p .. butane and butane respectively +117,4° C and -0.5° C.

Fig. 5. HYDROGEN bonds IN ALCOHOLS (shown by a dotted line)

alcohols have some common patterns: reactivity of primary Monohydric alcohols

are higher than the secondary, in turn, secondary alcohols are chemically more active than tertiary. For dihydric alcohols, in the case when the Oh groups are located at adjacent carbon atoms, there is increased (in comparison with Monohydric alcohols) reactivity due to the mutual influence of these groups. For alcohols the possible reactions taking place with a gap as C-O and O-H - bonds. When interacting with mineral or organic acids alcohols to form esters are compounds containing the fragment R-O-A (a - acid residue). The formation of esters occurs by the interaction of alcohols with anhydrides and chlorides of carboxylic acids (Fig. 6).

reversible and when conditions change can proceed in the opposite

direction, causing them to produce alcohol, for example by the hydrolysis of esters and kalogeropoulou (Fig.11A and B, respectively), as well as the hydration of alkenes - attach water (Fig.11B).

Fig. 11. OBTAINING ALCOHOLS BY HYDROLYSIS AND HYDRATION OF ORGANIC COMPOUNDS

Reaction of alkenes hydrolysis (Fig. 11, scheme C) is the basis of industrial production of lower alcohols containing up to 4 atoms of C.

such as glucose SNO. The process proceeds in the presence

of yeast and leads to the formation of ethanol and CO2: SNO ® NON + SO Fermentation can be obtained not more than 15% aqueous solution of alcohol, because with a higher concentration of alcohol yeast die. Solutions of higher alcohol concentration obtained by distillation.

a variety of chemical reactions can be used to obtain

all sorts of organic compounds: aldehydes, ketenes, carboxylic acids, simple and complex esters, used as organic solvents in the manufacture of resins, dyes and pharmaceuticals

manufacture of formaldehyde used to produce phenol-formaldehyde resins, recently seen

as a promising methanol motor fuel. Large amounts of methanol used in the extraction and transport of natural gas. Methanol is the most toxic compound among all the alcohol lethal dose the ingestion of 100 ml.

acid, and also for the production of esters of carboxylic

acids used as solvents. In addition, ethanol is the main component of all alcoholic beverages, it is widely used in medicine as a disinfectant.

addition, it serves as raw material for production of aromatic

substances (butyl acetate, butyl aniline, etc.). In shampoos it is used as a component to increase the transparency of the solutions. Benzyl alcohol SN-CH2-OH in the free state (in the form of esters) found in the essential oils of Jasmine and hyacinth. It has antiseptic (disinfectant) properties in cosmetics it is used as a preservative in creams, lotions, dental elixirs, and perfume - like sweet substance.

in rose oil, it is used in perfumery. Ethylene glycol HOCH2-CH2OH

used in the production of plastics and antifreeze (an additive that reduces the freezing point of aqueous solutions), in addition, in the manufacture of textile and printing inks. Diethylene glycol HOCH2-CH2OCH2-CH2OH used to fill the hydraulic brake devices, as well as in the textile industry for finishing and dyeing.

it is a component of many cosmetic preparations. Nitroglycerin (Fig.

6), the major component of dynamite used in mining and railway construction as explosives. Pentaerythritol (HOCH2)4C used to produce polyesters (pentaftalevye resin) as a curing agent for synthetic resins, as a plasticizer of polyvinyl chloride, and in the manufacture of explosives tetranitromethane. Polyhydric alcohols xylitol NON-(SNON)3-SNON and orbital NON- (SNON)4-SNON have a sweet taste, they are used instead of sugar in confectionery products for diabetics and people suffering from obesity. Orbital contained in the berries of mountain ash and cherry. Glycerin HOCH2-CH(OH)-CH2OH used to produce polyester glyptic resins, in addition, it is a component of many cosmetic preparations. Nitroglycerin (Fig. 6), the major component of dynamite used in mining and railway construction as explosives.