Q:

How to distinguish between alkene and alcohol

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A:

1. chemical formula and structural formula

1.1 chemical difference

the chemical formulae of olefins and alcohols can be distinguished by molecular formulae. The molecular formula of olefins is usually C- H-O, while the molecular formula of alcohols is C- H-O. It is easy to see from the molecular formula that olefins do not contain oxygen, while alcohols contain a hydroxyl group (-OH), so the number of oxygen atoms determines their category.

1.2 structural analysis

from the structural formula, the functional groups of olefins and alcohols are completely different. The core feature of olefins is a double bond (C = C). For example, the structural formula of ethylene is C? H? and propylene is C? H. The presence of double bonds makes olefins unsaturated and prone to addition reactions. The structural formula of the alcohol contains hydroxyl (-OH), such as the structural formula of ethanol is CH, CH OH, and the presence of hydroxyl groups gives the water solubility of the alcohol and the chemical properties of the alcohol.

2. physical properties difference

2.1 Appearance Color and Status

olefins are usually colorless transparent liquids with a lower density, while alcohols such as ethanol are colorless liquids, and the color and state may change slightly as the molecular weight increases. From the appearance, olefins and alcohols are easy to be misjudged, so the distinction of physical properties needs to be combined with other indicators.

2.2 solubility and odor

olefins are less soluble in water and have no significant odor, e.g. ethylene is odorless, while propylene is likewise odorless. In contrast, alcohol has a typical fruity odor, such as the odor of ethanol, which is easy to distinguish in daily life. This distinction is very useful in everyday life and helps in rapid identification.

3. chemical differences

3.1 reaction characteristics

the chemical reaction characteristics of olefins and alcohols are quite different. Olefins, as highly unsaturated compounds, are prone to chemical reactions such as addition reactions and polymerization reactions. For example, ethylene may undergo an addition reaction with H₂ in the presence of a catalyst to form Ethane. Alcohols are prone to acidolysis under acidic conditions, for example, ethanol can react with ether under the catalysis of sulfuric acid.

The chemical reaction characteristics of 3 are very different. Olefins, as highly unsaturated compounds, are prone to chemical reactions such as addition reactions and polymerization reactions. For example, ethylene may undergo an addition reaction with H₂ in the presence of a catalyst to form Ethane. Alcohols are prone to acidolysis under acidic conditions, for example, ethanol can react with ether under the catalysis of sulfuric acid.

3.2 acid-base reaction

in terms of acid-base reactions, olefins do not participate in acid-base reactions, while alcohols can act as participants in acid-base reactions, especially in redox reactions. For example, alcohols are readily oxidized under acidic conditions to form aldehydes or carboxylic acids, for example, ethanol can be oxidized to form acetaldehyde in the presence of oxygen and a catalyst.

4. Application Differentiation

In practical applications, it is very important to distinguish between olefins and alcohols. For example, in organic synthesis, the synthesis conditions and reaction mechanisms of olefins and alcohols are significantly different, and the selection of suitable raw materials and catalysts can significantly improve the reaction efficiency. In the process of separation and purification, olefins and alcohols can be effectively separated by the difference of density, solubility and odor.

5. summary

Through the chemical formula, structural formula, physical properties and chemical properties of various analysis, can be clearly divided between olefins and alcohols. Remember that olefins contain double bonds, are oxygen-free and insoluble in water, while alcohols contain hydroxyl groups, are odorous and readily soluble in water. Mastering these differences will help to identify and apply substances more efficiently in practical work. Through in-depth understanding and application of this knowledge, readers can become more comfortable in the chemical industry.

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