Question

Draw condensed structural formulas for the following compounds. Use line structures for rings. a. 1,4-diethylcyclohexene b. 2,4-dimethyl-1-octene c. 2,2-dimethyl-3-hexyne

Short answer

The condensed structural formulas for the given compounds are: a. 1,4-diethylcyclohexene: \(CH_2C(CH_2CH_3)CHC(CH_2CH_3)CHCHCH_2\) b. 2,4-dimethyl-1-octene: \(CH_2C(CH_3)CH(CH_3)CH_2CH_2CH_2CH_3\) c. 2,2-dimethyl-3-hexyne: \(CH_3C(CH_3)CCCHCH_3\)

Step-by-step solution

Identify functional groups and carbon chain in each compound

For each compound, we need to identify the functional groups present, the length of the carbon chain, and the positions of any substituents. a. 1,4-diethylcyclohexene Functional group: alkenes (double bond) Carbon chain: cyclohexene (6-membered ring) Substituents: ethyl groups at positions 1 and 4 b. 2,4-dimethyl-1-octene Functional group: alkenes (double bond) Carbon chain: octene (C8H16) Substituents: methyl groups at positions 2 and 4 c. 2,2-dimethyl-3-hexyne Functional group: alkynes (triple bond) Carbon chain: hexyne (C6H10) Substituents: methyl groups at position 2, occurring twice

Draw the main carbon chain and functional groups

a. Draw a 6-membered ring with a double bond between carbons 1 and 2, representing cyclohexene. b. Draw an 8-carbon chain with a double bond between carbons 1 and 2, representing 1-octene. c. Draw a 6-carbon chain with a triple bond between carbons 3 and 4, representing 3-hexyne.

Add the substituents to the carbon chain

a. Add ethyl groups (C2H5) to carbons 1 and 4 of the cyclohexene ring. b. Add methyl groups (CH3) to carbons 2 and 4 of the 1-octene chain. c. Add two methyl groups (CH3) to carbon 2 of the 3-hexyne chain.

Draw the condensed structural formulas

a. The condensed structural formula for 1,4-diethylcyclohexene is given as: \(CH_2C(CH_2CH_3)CHC(CH_2CH_3)CHCHCH_2\). b. The condensed structural formula for 2,4-dimethyl-1-octene is given as: \(CH_2C(CH_3)CH(CH_3)CH_2CH_2CH_2CH_3\). c. The condensed structural formula for 2,2-dimethyl-3-hexyne is given as: \(CH_3C(CH_3)CCCHCH_3\).

Key concepts

Functional Groups

Functional groups are specific groups of atoms within a molecule that are responsible for the characteristic chemical reactions of that molecule. Recognizing these groups is crucial when determining the properties and behaviors of organic compounds.

In the context of our exercise, we analyzed the functional groups for three different compounds:

• 1,4-diethylcyclohexene has an alkene group, characterized by a double bond between carbon atoms. Alkenes are known for their reactivity due to this double bond.
• 2,4-dimethyl-1-octene also features an alkene functional group. In such structures, the position of the double bond can influence the compound's properties.
• 2,2-dimethyl-3-hexyne contains an alkyne group where the triple bond introduces different properties compared to alkenes. Alkynes can be more reactive and tend to have linear geometry around the triple bond.

Understanding functional groups helps in predicting chemical reactions and behaviors of organic molecules. Thus, these groups are central to the study of organic chemistry.

Carbon Chain

The carbon chain in an organic molecule is the backbone of the compound, consisting of a series of carbon atoms connected together. It defines the core structure upon which functional groups and substituents are attached.

Let's look at the carbon chains in the given compounds:

• For 1,4-diethylcyclohexene, the carbon chain forms a six-membered ring known as cyclohexene. Rings alter the properties of the molecule, making them more rigid.
• In 2,4-dimethyl-1-octene, we encounter a straight eight-carbon chain called octene. This linear structure allows for more flexibility in the molecule.
• 2,2-dimethyl-3-hexyne features a six-carbon linear chain with a triple bond giving it properties distinct from alkenes, like increased acidity and tighter bond angles.

The length and type of carbon chain significantly affect the physical and chemical characteristics of the compound, such as its boiling point, solubility, and reactivity.

Substituents

Substituents are atoms or groups of atoms that replace hydrogen atoms attached to the carbon chain in a molecule. They are critical in defining a compound's identity and influence its properties, reactivity, and functionality.

In our compounds, substituents were carefully placed as follows:

• 1,4-diethylcyclohexene features ethyl groups on carbons 1 and 4. These larger groups increase steric hindrance and can affect the molecule's 3D shape and reactions.
• 2,4-dimethyl-1-octene has methyl groups at positions 2 and 4. Methyl groups tend to enhance hydrophobic character and can influence molecular interactions.
• In 2,2-dimethyl-3-hexyne, two methyl groups are present on carbon 2, intensifying the steric and electronic influence at that point in the molecule.

Substituents help add diversity to organic molecules, allowing for endless combinations and complex characteristics in synthetic and natural compounds.