Condensed Structural Formula For 1 4 Dichlorocyclohexane

Condensed structural formula for 1 4 dichlorocyclohexane – Unveiling the intricacies of 1,4-dichlorocyclohexane, this exploration delves into its condensed structural formula, providing a comprehensive understanding of its molecular makeup and chemical characteristics.

As a cyclic hydrocarbon bearing two chlorine atoms, 1,4-dichlorocyclohexane exhibits a unique arrangement of atoms represented by its condensed structural formula: C6H10Cl2. This formula succinctly conveys the molecular composition, highlighting the presence of six carbon atoms, ten hydrogen atoms, and two chlorine atoms.

1. Structural Formula

Condensed structural formula for 1 4 dichlorocyclohexane

The condensed structural formula for 1,4-dichlorocyclohexane is C 6H 10Cl 2. It can be represented visually as:

Cl\ / C – C – C – C – C – C / \ / \ / \ C Cl H H H H

The IUPAC nomenclature for 1,4-dichlorocyclohexane is 1,4-dichloro-cyclohexane.

2. Chemical Properties

Condensed structural formula for 1 4 dichlorocyclohexane

Physical Properties

  • Boiling point: 208-210 °C
  • Melting point: -40 °C
  • Density: 1.23 g/cm 3

Chemical Properties

1,4-Dichlorocyclohexane is a reactive compound due to the presence of two chlorine atoms. It undergoes nucleophilic substitution reactions, where the chlorine atoms are replaced by other nucleophiles.

Examples of reactions involving 1,4-dichlorocyclohexane include:

  • Reaction with sodium hydroxide to form 1,4-cyclohexanediol
  • Reaction with ammonia to form 1,4-cyclohexanediamine
  • Reaction with alcohols to form 1,4-cyclohexyl ethers

3. Production Methods: Condensed Structural Formula For 1 4 Dichlorocyclohexane

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1,4-Dichlorocyclohexane is produced by the following methods:

Chlorination of Cyclohexane, Condensed structural formula for 1 4 dichlorocyclohexane

This is the most common method, where cyclohexane is reacted with chlorine gas in the presence of a catalyst.

Addition of Hydrogen Chloride to 1,3-Butadiene

1,3-Butadiene is reacted with hydrogen chloride in the presence of a catalyst to form 1,4-dichlorocyclohexane.

Advantages and Disadvantages

The advantages and disadvantages of each method are:

Method Advantages Disadvantages
Chlorination of Cyclohexane High yield Formation of byproducts
Addition of Hydrogen Chloride to 1,3-Butadiene Less byproduct formation Lower yield

4. Safety Considerations

Condensed structural formula for 1 4 dichlorocyclohexane

Hazards

  • 1,4-Dichlorocyclohexane is a toxic substance.
  • It is harmful if swallowed, inhaled, or absorbed through the skin.
  • It can cause irritation to the eyes, skin, and respiratory tract.

Handling and Storage

1,4-Dichlorocyclohexane should be handled and stored with care. It should be stored in a cool, dry place away from sources of heat and ignition. It should be handled in a well-ventilated area and appropriate personal protective equipment should be worn.

Environmental Impact

1,4-Dichlorocyclohexane is a persistent organic pollutant (POP). It can accumulate in the environment and pose a threat to wildlife. Mitigation strategies include proper disposal of waste containing 1,4-dichlorocyclohexane and reducing its use in industrial processes.

FAQ Corner

What is the IUPAC name for 1,4-dichlorocyclohexane?

1,4-Dichlorocyclohexane

What are the physical properties of 1,4-dichlorocyclohexane?

Boiling point: 172-174 °C, Melting point: -22.6 °C, Density: 1.17 g/cm³

What are the common uses of 1,4-dichlorocyclohexane?

Solvent, intermediate in the production of other chemicals, and a precursor for the synthesis of pharmaceuticals

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