Vulcanisation is a chemical system in which the rubber is heated with sulfur, accelerator, and activator 140–160°C.
The method involves the formation of cross-links between long rubber molecules so as to achieve improved elasticity, resilience, tensile strength, viscosity, hardness, and weather resistance.
Benzene is commercially isolated from coal tar. However, it may be prepared in the laboratory by the following methods:
Cyclic polymerization of ethyne- here, alkyne molecules add to each other resulting in the formation of a cyclic compound when ethyne is passed through a red hot iron tube at 873 K it undergoes cyclic polymerization. In this process, 3 molecules of ethyne polymerize to form benzene
Decarboxylation of aromatic acids- It is a chemical reaction that removes a carboxyl group and releases carbon dioxide (CO2).
Usually, decarboxylation refers to a reaction of carboxylic acids, removing a carbon atom from a carbon chain.
The reverse process, which is the first chemical step in photosynthesis, is called carboxylation, the addition of CO2 to a compound.
Enzymes that catalyze decarboxylations are called decarboxylases or, the more formal term, carboxy-lyases.
The term "decarboxylation" usually means replacement of a carboxyl group (-COOH) with a hydrogen atom
RCO2H → RH + COO Sodium salt of benzoic acid on heating with soda-lime gives benzene.
Reduction of phenol:
- Phenol is reduced to benzene by, passing its vapors over, heated zinc dust.
- Phenol can be converted to benzene by using strong reducing agents like Zn dust with strong heating.
- When strongly heated, the phenol gets converted into phenoxide ion and proton thus released accepts an electron from Zn forming H radical.