Question

Predict A monohalogenation reaction describes a substitution reaction in which a single hydrogen atom is replaced by a halogen. A dihalogenation reaction is a reaction in which two hydrogen atoms are replaced by two halogen atoms. a. Draw the structures of all the possible monohalogenation products that can form when pentane reacts with \(\mathrm{Cl}_{2}\) . b. Draw the structures of all the possible dihalogenation products that can form when pentane reacts with \(\mathrm{Cl}_{2}\)

Short answer

The monohalogenation products of pentane reacting with Cl₂ are 1-chloropentane and 2-chloropentane. For dihalogenation, there are 10 possible products: 1,1-dichloropentane, 1,2-dichloropentane, 1,3-dichloropentane, 1,4-dichloropentane, 1,5-dichloropentane, 2,2-dichloropentane, 2,3-dichloropentane, 2,4-dichloropentane, 3,3-dichloropentane, and 3,4-dichloropentane.

Step-by-step solution

Monohalogenation of Pentane

Monohalogenation involves replacing one hydrogen atom with a chlorine atom. Start by examining the structure of pentane (C5H12). There are two different types of carbon atoms based on their position in the chain: - 2 primary carbons: at the ends of the chain - 3 secondary carbons: the central carbons For each type of carbon, the monohalogenation reaction can form one chlorinated product. Replace one hydrogen atom on the primary and secondary carbons with a chlorine atom to obtain the structures. The monohalogenation products are: 1. 1-chloropentane (Chlorine atom at a primary carbon) 2. 2-chloropentane (Chlorine atom at a secondary carbon)

Dihalogenation of Pentane

Dihalogenation involves replacing two hydrogen atoms with two chlorine atoms. Again, start by examining the structure of pentane (C5H12). We will look at all possible combinations where two chlorine atoms can replace the hydrogen atoms on the pentane molecule. The dihalogenation products are: 1. 1,1-dichloropentane (Both chlorine atoms on the same primary carbon) 2. 1,2-dichloropentane (One chlorine atom at a primary carbon and the other at an adjacent secondary carbon) 3. 1,3-dichloropentane (One chlorine atom at a primary carbon and the other at a non-adjacent secondary carbon) 4. 1,4-dichloropentane (Both chlorine atoms at the primary carbons) 5. 1,5-dichloropentane (One chlorine atom at a primary carbon and the other at an opposite primary carbon) 6. 2,2-dichloropentane (Both chlorine atoms on the same secondary carbon) 7. 2,3-dichloropentane (One chlorine atom at a secondary carbon and the other at an adjacent secondary carbon) 8. 2,4-dichloropentane (One chlorine atom at a secondary carbon and the other at a non-adjacent secondary carbon) 9. 3,3-dichloropentane (Both chlorine atoms on the same secondary carbon) 10. 3,4-dichloropentane (One chlorine atom at a secondary carbon and the other at an adjacent secondary carbon) These are all the possible monohalogenation and dihalogenation products of pentane when it reacts with Cl₂.

Key concepts

Monohalogenation

Monohalogenation is a fascinating chemical reaction where a single hydrogen atom in a molecule is replaced by a halogen atom, like chlorine. Imagine you have a string of beads, and you replace one bead with a brightly colored one. That's similar to what happens in monohalogenation. Here, we focus on pentane, a simple hydrocarbon with the formula \(\text{C}_5\text{H}_{12}\). For pentane, the monohalogenation reaction with chlorine involves replacing one hydrogen atom with a chlorine atom, forming chloropentanes.

Pentane has two types of carbons: primary carbons at the ends and secondary carbons centrally. Each carbon type will lead to different chloropentane products when involved in the reaction.

• 1-chloropentane: When the chlorine attaches to a primary carbon.
• 2-chloropentane: When the chlorine attaches to a secondary carbon.

Monohalogenation is specific because only one chlorine atom is added, making the reaction product have distinct characteristics.

Dihalogenation

Dihalogenation is the process of adding two halogen atoms to a hydrocarbon chain, replacing two hydrogen atoms in the process. If monohalogenation is like adding one colored bead, dihalogenation is like adding two. For pentane, the molecule reacts with chlorine to form various dichloropentane products. This reaction can occur at different positions on the carbon chain, resulting in multiple unique compounds.

The beauty of dihalogenation lies in the variety of products it can yield. With pentane's five carbon backbone, the possibilities include:

• 1,1-dichloropentane: Both chlorines on the same primary carbon.
• 1,2-dichloropentane: Chlorines at adjacent carbons (one primary, one secondary).
• 1,3-dichloropentane: Chlorines on a primary and a non-adjacent secondary carbon.
• 3,3-dichloropentane: Both chlorines on the same secondary carbon.

Each product's structure varies, creating chemicals with different properties and uses.

Pentane

Pentane is a simple alkane, a straight-chain hydrocarbon with five carbon atoms. It has the chemical formula \(\text{C}_5\text{H}_{12}\). Think of pentane as a chain of five carbon "beads," each connected by single bonds, with hydrogen atoms filling the remaining available bonds.

In a classroom analogy, pentane can be seen as a basic linear structure, allowing students to easily visualize modifications at specific positions. This makes it an ideal molecule for studying halogenation reactions, as we can explore how different substitutions affect the overall structure. Since all carbon atoms in pentane are connected linearly, it serves as a great model for understanding both monohalogenation and dihalogenation processes.

Pentane's straightforward nature simplifies the study of more complex molecules and reactions in organic chemistry.

Substitution Reaction

A substitution reaction is a fundamental type of organic reaction where an atom or a group of atoms in a molecule is replaced with a different atom or group. In the context of halogenation, substitution involves replacing hydrogen atoms with halogen atoms such as chlorine. Imagine swapping out one puzzle piece for another that fits perfectly in the same place.

These reactions are critical in organic chemistry because they allow the transformation of simple hydrocarbons into more complex molecules with unique physical and chemical properties.
Key aspects of substitution reactions include:

• The identity of the atom or group being replaced and the new replacing group.
• The conditions under which the reaction occurs, like temperature and the presence of catalysts.

In halogenation, substitution reactions are specific, as they replace particular hydrogen atoms with halogens, leading to distinct products discussed in monohalogenation and dihalogenation.