2,3-Dimethylbutanereacts with bromine in the presence of light to give a mono brominate product. Further reaction gives a good yield of a dibrominated product. Predict the structures of these products, and propose a mechanism for the formation of the monobrominated product.

Short Answer

Expert verified

The Themonobrominated product formed is 2-bromo-2, 3-dimethylbutane and the dibrominated product formed is 2, 3-dibromo-2, 3-dimethylbutane.

The mechanism for the formation of mono brominated product.


The mechanism for the formation of dibrominated product

Step by step solution

01

Free radicals

An atom or group of atoms containing odd or unpaired electrons is known as free radical. The unpaired electron is represented by a single unpaired dot in the formula. Free radicals are electrically neutral. They are highly reactive species formed by homolytic fission of a covalent bond.

02

Steps involved in free radical chain reaction

In a free-radical chain reaction, free radicals are generally created in the initiation step. A free radical and a reactant are combined to yield a product in the propagation step. Lastly, the number of free radicals generally decreases in the termination step

03

Reaction of 2,3-Dimethylbutane  with bromine in presence of light

Reaction of 2,3-Dimethylbutanewith bromine in presence of light

Themonobrominated product formed is 2-bromo-2,3-dimethylbutaneand the dibrominated product formed is2,3-dibromo-2,3-dimethylbutane .

04

Mechanism for the formation of monobrominated product

The mechanism consists of three parts—initiation step, propagation step I, and propagation step II.

Mechanism for the formation of monobrominated product

05

Mechanism for the formation of dibrominated product

The mechanism consists of three parts—initiation step, propagation step I, and propagation step II.

Mechanism for the formation of dibrominated product

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Most popular questions from this chapter

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