Question

Draw the structure for each molecule. $$ \begin{array}{ll}{\text { a. } 1 \text { -propanol }} & {\text { c.propyl ether }} \\ {\text { b. } 1,3 \text { -cyclopentanediol }} & {\text { d. } 1,2 \text { -propanediamine }}\end{array} $$

Short answer

The structures of the given molecules are as follows: a. 1-propanol: \(CH_3-CH_2-CH_2OH\) b. 1,3-cyclopentanediol: a cyclopentane ring with hydroxyl groups at the first and third carbon atoms. c. Propyl ether: \(CH_3-CH_2-CH_2-O-CH_2-CH_2-CH_3\) d. 1,2-propanediamine: \(H_2N-CH_2-CH_2-NH_2\)

Step-by-step solution

a. 1-propanol

1-propanol is an alcohol with three carbon atoms and the hydroxyl group (-OH) attached at the first carbon atom. To draw its structure, follow these steps: 1. Draw a chain of 3 carbon atoms: \(CH_3-CH_2-CH_2\). 2. Attach the hydroxyl group (-OH) to the first carbon atom, resulting in the structure: \(CH_3-CH_2-CH_2OH\). Thus, the structure of 1-propanol is \(CH_3-CH_2-CH_2OH\).

b. 1,3-cyclopentanediol

1,3-cyclopentanediol is a cyclic alcohol with five carbon atoms in the cycle and hydroxyl groups at the first and third carbon atoms. To draw its structure, follow these steps: 1. Draw a pentagon with five carbon atoms to represent the cyclopentane ring. 2. Attach hydroxyl groups (-OH) to the first and third carbon atoms in the ring. Thus, the structure of 1,3-cyclopentanediol consists of a cyclopentane ring with hydroxyl groups at the first and third carbon atoms.

c. Propyl ether

Propyl ether is an ether with two propyl groups (three carbon atom chains) connected by an oxygen atom. To draw its structure, follow these steps: 1. Draw two separate chains of 3 carbon atoms each: \(CH_3-CH_2-CH_2\). 2. Connect the third carbon atom of each chain with an oxygen atom, resulting in the structure: \(CH_3-CH_2-CH_2-O-CH_2-CH_2-CH_3\). Thus, the structure of propyl ether is \(CH_3-CH_2-CH_2-O-CH_2-CH_2-CH_3\).

d. 1,2-propanediamine

1,2-propanediamine is an amine with three carbon atoms and amine groups (-NH_2) attached at the first and second carbon atoms. To draw its structure, follow these steps: 1. Draw a chain of 3 carbon atoms: \(CH_3-CH_2-CH_2\). 2. Replace the hydrogen atoms at the first and second carbon atoms with amine groups (-NH_2), resulting in the structure: \(H_2N-CH_2-CH_2-NH_2\). Thus, the structure of 1,2-propanediamine is \(H_2N-CH_2-CH_2-NH_2\).

Key concepts

1-Propanol

1-Propanol is a type of alcohol, which is a class of organic compounds characterized by the presence of one or more hydroxyl (-OH) groups. In 1-propanol, there are three carbon atoms forming a straight chain. The hydroxyl group is attached to the first carbon atom, distinguishing it as a primary alcohol.

• Structure: The chemical structure of 1-propanol is represented as \(CH_3-CH_2-CH_2OH\).
• Properties: As an alcohol, 1-propanol is known for being a good solvent and is miscible with water, owing to the polar nature of the hydroxyl group, which can form hydrogen bonds with water molecules.
• Uses: It is frequently used in pharmaceuticals, as a solvent, and in chemical synthesis for various industrial applications.

Understanding the basics of 1-propanol provides foundational knowledge of primary alcohols and their importance in both science and industry.

Cyclopentanediol

Cyclopentanediol is a diol, meaning it has two hydroxyl groups, and it is part of a class of alcohols known as cyclic alcohols. Specifically, 1,3-cyclopentanediol consists of a five-carbon ring, which forms a cyclopentane structure.

• Structure: The cyclopentane ring has hydroxyl groups attached to the first and third carbon atoms.
• Properties: The cyclic nature of cyclopentanediol can contribute to unique physical and chemical properties compared to linear diols.
• Applications: Cyclic diols like stereoisomers of cyclopentanediol are valuable in synthesizing pharmaceuticals and designing biologically active compounds.

Learning about cyclopentanediol helps deepen the understanding of cyclic alcohols and their versatile roles in chemistry.

Propyl Ether

Propyl ether, an ether, showcases organic chemistry's functional group diversity. Ethers are characterized by an oxygen atom connected to two alkyl or aryl groups, in this case, two propyl groups.

• Structure: In propyl ether, the oxygen atom is bonded to the third carbon of two propyl groups, presented as \(CH_3-CH_2-CH_2-O-CH_2-CH_2-CH_3\).
• Properties: Ethers like propyl ether tend to have lower boiling points compared to alcohols with similar molecular weights, due to the absence of hydrogen bonding between ether molecules.
• Uses: Propyl ether serves as a solvent in chemical reactions, due to its relative inertness and ability to dissolve a broad range of substances.

Gaining insight into ethers such as propyl ether enhances one's grasp of functional group interactions in organic chemistry.

Propanediamine

Propanediamine falls under amines, compounds that are derivatives of ammonia where one or more hydrogen atoms are replaced by organic groups. In 1,2-propanediamine, each of the first and second carbon atoms in a three-carbon chain is attached to an amine group (-NH_2).

• Structure: It is depicted structurally as \(H_2N-CH_2-CH_2-NH_2\), showcasing two amine groups in the structure.
• Properties: Amines like propanediamine are often basic and can participate in hydrogen bonding, which affects their boiling points and solubility in water.
• Applications: As an intermediate in organic synthesis, propanediamine's versatility allows for the creation of polymers, pharmaceuticals, and other complex compounds.

Understanding propanediamine provides clarity into the behavior and significance of amines in organic chemistry and their vast applications.