Question

Write the initiation, propagation, and termination steps involved in the monobromination of \(2,3-\) dimethylbutane to give 2 -bromo- 2,3 -dimethylbutane.

Short answer

The bromination of 2,3-dimethylbutane involves three steps. Initiation: Br2 becomes 2Br* under light. Propagation: The bromine radical abstracts hydrogen from 2,3-dimethylbutane to form a primary radical, which reacts with another bromine molecule to form 2 -bromo- 2,3 -dimethylbutane. Termination: Radicals recombine to form neutral species, breaking the chain reaction.

Step-by-step solution

Initiation

This step involves homolytic fission. Here, the bond in the bromine molecule (Br2) breaks evenly to form two bromine radicals. Hence the equation is \[ Br2 \xrightarrow{h\nu} 2Br* \], where \(h\nu\) signifies light energy, and the asterisk (*) represents a radical.

Propagation

There are actually two propagation steps. For this exercise, the first step involved in propagation is the abstraction of a hydrogen atom from 2,3-dimethylbutane by a bromine radical to form a primary radical (2,3-dimethylbutyl radical), shown here: \[ (CH3)2CHCH(CH3)2 + Br* \rightarrow (CH3)2C*HCH(CH3)2 + HBr \] Also, the primary radical (2,3-dimethylbutyl radical) formed as a result will react with another molecule of bromine to form 2 -bromo- 2,3 -dimethylbutane. So \[ (CH3)2C*HCH(CH3)2 + Br2 \rightarrow (CH3)2CBrCH(CH3)2 + Br* \]

Termination

The termination step involves the recombination of radicals to form neutral species. Since the radicals available towards the end of the reaction are few, for the bromination of 2,3-dimethylbutane, the termination step could be one of the 2 possibilities: \[ Br* + Br* \rightarrow Br2 \] or \[ (CH3)2C*HCH(CH3)2 + Br* \rightarrow (CH3)2CBrCH(CH3)2 \] Both these reactions lead to disruptions of the chain reaction.

Key concepts

Radical Reactions

Radical reactions are quite fascinating in organic chemistry due to their unique mechanism of involving unpaired electrons. These types of reactions usually start with the formation of radicals, which are species having one or more unpaired electrons. These unpaired electrons are typically very reactive because they seek to pair up to reach a more stable state.
A typical radical reaction follows three primary stages:

• Initiation: In this first step, radicals are generated. This often occurs through the homolytic cleavage of a bond, a process that generates two radicals. For example, in the initiation step of the monobromination of 2,3-dimethylbutane, a bromine molecule \(Br_2\) undergoes homolytic fission to form two bromine radicals \(Br^*\). Light energy, denoted as \(hu\), provides the necessary energy for this bond cleavage.
• Propagation: This step involves a chain of radical reactions. The radicals produced in the initiation step react with stable molecules to form new radicals, which in turn propagate the chain reaction. In the case of bromination, a bromine radical abstracts a hydrogen atom from the organic substrate resulting in a new radical, while the bromine radical itself is regenerated.
• Termination: The chain reaction can stop when two radicals combine to form a stable, non-radical product. This results in the loss of reactive species, ending the reaction. Typical termination reactions in bromination include forming \(Br_2\) or the final brominated organic compound.

Understanding these steps is crucial when exploring how radical reactions proceed and transform organic molecules.

Halogenation

Halogenation is a fundamental concept in organic chemistry where one or more hydrogen atoms in an organic compound are replaced by halogen atoms like bromine or chlorine. This reaction is highly significant due to its application in synthesizing more complex molecules and various industrial processes.
The reaction often proceeds through a radical mechanism, as seen in the monobromination of 2,3-dimethylbutane. Here's a breakdown of the process:

• Initiation Step: Bromine molecules \(Br_2\) are split into radicals using light or heat. This creates reactive intermediates that drive the reaction.
• Propagation Steps: The bromine radical abstracts a hydrogen atom from the 2,3-dimethylbutane, forming a new radical. This new radical reacts with another bromine molecule to form the brominated product and regenerate a bromine radical.
• Termination Steps: The reaction eventually stops when radicals combine to form stable compounds, either returning to their original state or forming the desired brominated product.

Halogenation reactions, especially with bromine, are selective and can provide specificity by choosing conditions that favor one product over others, such as using different temperatures or solvents. Learning these nuances aids in predicting and controlling outcomes in organic synthesis.

Organic Chemistry

Organic chemistry focuses on the study of carbon-containing compounds, their properties, reactions, and structures. It encompasses a vast area of chemistry due to carbon's ability to form stable bonds with many elements, including itself.
Radical reactions and halogenation are just two dynamic facets of organic chemistry that allow the transformation and synthesis of a wide range of organic molecules. Here are some essential insights:

• Bond Formation and Cleavage: Organic chemistry heavily involves the making and breaking of chemical bonds, influenced by factors like bond strength and reaction energy barriers.
• Reactivity and Stability: Radicals are trading stability for reactivity. This balance between reactivity and stability determines which reactions are possible and under what conditions.
• Stereochemistry and Selectivity: Organic reactions are not merely about what products are formed but also about how they are formed. Stereochemistry, which considers the 3D structure of molecules, can influence the outcome and selectivity of reactions.

Understanding the fundamental principles of organic reactions equips chemists to design and execute various synthetic strategies, ultimately contributing to advances in fields such as materials science, pharmaceuticals, and biochemistry.