What are the qualitative reactions for alkenes? In order to answer this question, we must first understand what is the feature of representatives of this class.
For starters, let's analyze the structure of alkenes. Unsaturated hydrocarbons are called compounds having the General formula CnH2n. The structure of the linear alkenes, but their structure in addition to single (simple) connection is present and complex (double bond).
Before to characterize the qualitative reactions for alkenes, stop about their names. The sequence of actions is similar to the alkanes class, but there are some distinctive options, which should stay separate. First we need the proposed structure to find the longest carbon chain that includes the double bond.
Next, the atoms are numbered from the side on which is located the double bond closer to the beginning of the chain. If in a molecule are hydrocarbon radicals (other variants of the substituents), in this case, be sure to indicate the number of their position. If you have multiple identical radicals used by specifying prefix. Then called itself the main chain, using the suffix-EN. A requirement (in addition to ethylene and propene) is an indication of the number of the position of multiple bonds.
Qualitative reactions for alkenes associated with the location in the molecules of the double bond. This dependence suggests a more detailed study of the issue concerning the isomerism of unsaturated hydrocarbons. Like other representatives of the hydrocarbons, the molecules of alkenes are structural isomers. For example, substance composition С4Н8 can portray butene and 2-methylpropene.
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In addition, the representatives of this class of unsaturated hydrocarbons and isomerism of double bond position. From its location depend on some chemical properties of this class.
Among the distinctive types of isomerism not possessed by other members of the C x h y, we note the geometric (spatial structure). Depending on the rotation at the double bond of an alkene molecule fragments, it is possible to obtain CIS - and TRANS - isomers. Interclass isomerism alkenes connects with cycloalkane. Such a variety of structures, typical for the homologous series ethylene, determines their basic chemical properties.
Qualitative reactions for alkenes is their interaction with aqueous solutions of Halogens. These include bromine, iodine, chlorine. As a result of this chemical reaction is cleavage of double bonds, the accession of halogen atoms. As a feature of this interaction is seen discoloration of iodine (bromine) water. Qualitative reactions on the double bond of alkenes is their reaction with water solution of potassium permanganate in an acidified environment.
As products of this reaction are sulfate and organic product. It was a reaction with an oxidizing agent and a solution of Halogens is qualitative reactions for alkenes. Hydrogenation is not required, it will receive the corresponding limit hydrocarbons (alkanes). As mandatory conditions of their occurrence stands high temperature, and the use of a catalyst.
The Activity of alkenes is much more than the paraffins. The reason is the presence between the carbon atoms at the double bond is not too strong bonds.
During the combustion of any hydrocarbon composition CnH2n in oxygen is observed the allocation of water vapor, carbon dioxide, and the formation of a sufficient amount of heat. Qualitative reactions to alkenes can be used for the selection of these compounds among other substances.
The hydration Reaction (water connections) is for asymmetrical alkenes according to Markovnikov rule. According to him the accession of a hydrogen atom to the carbon, which contains more hydrogen. The hydroxide ion will attach to the carbon by double bonds, wherein less than N.
On a similar mechanism and rule alkenes react chemically with molecules of the hydrogen halides.
Interest and the reaction of polymerization, which formed high-molecular compounds. So, selecting as the initial monomer of ethylene catalytic polymerization produces polyethylene, which is a valuable raw material for chemical industry.
The First members of the homologous series of ethylene are gaseous substances are practically odorless. They are poorly soluble in water, soluble in organic compounds. There is a direct correlation between the increase in relative molecular mass and boiling points (melting point), transition from gaseous state to liquid, solid state of aggregation.
Where usedrepresentatives of the unsaturated hydrocarbons of the ethylene series? Ethylene is a valuable feedstock for chemical production. It is possible to obtain styrene, vinyl chloride, ethanol, acetic aldehyde, acid, and dichloroethane. In the polymerization of alkenes formed polyvinyl acetate, lubricants, rubbers. On average, global production of polyethylene is 100 million tons per year. Industrial quantities of propylene required for the synthesis of the polymer. In addition, the propene is the raw material for the manufacture of oxide, isopropanol, cumene, butyric aldehyde, glycerine.
Butyny basically needed to create a polyisobutylene, methyl ethyl ketone, butyl rubber, isoprene. Isobutylene is an excellent chemical feedstock in the manufacture of tertiary butanol, butyl rubber, and isoprene. It is the isobutylene necessary for alkylation of phenols in the manufacture of surfactants. Copolymers with butene used as a sealant and oil additives. Higher unsaturated hydrocarbons of the ethylene series are used not only in the production of polymeric materials, but also organic production of higher alcohols.
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Alin Trodden - author of the article, editor
"Hi, I'm Alin Trodden. I write texts, read books, and look for impressions. And I'm not bad at telling you about it. I am always happy to participate in interesting projects."
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