Question

You are asked to identify an unknown colorless, liquid carbonyl compound. Analysis has determined that the formula for this unknown is \(\mathrm{C}_{3} \mathrm{H}_{6} \mathrm{O} .\) Only two compounds match this formula. (a) Draw structures for the two possible compounds. (b) To decide which of the two structures is correct, you react the compound with an oxidizing agent and isolate from that reaction a compound that is found to give an acidic solution in water. Use this result to identify the structure of the unknown. (c) Name the acid formed by oxidation of the unknown.

Short answer

The unknown compound is 1-propanal, which oxidizes to form propanoic acid.

Step-by-step solution

Calculate Degree of Unsaturation

To determine the degree of unsaturation, use the formula: \(d = C + 1 - (H + X - N)/2\). Here, there are 3 carbon atoms, 6 hydrogen atoms, and 1 oxygen atom. Nitrogen and halogens are not present, so the formula simplifies to: \(d = 3 + 1 - 6/2 = 2\). This indicates there are two degrees of unsaturation, suggesting the presence of either a ring or multiple bonds.

Draw Possible Structures

Considering the degrees of unsaturation and the molecular formula \(C_3H_6O\), the possible structures are 1-propanal and 2-propanone. \[\text{1-Propanal: } \text{CH}_3\text{CH}_2\text{CHO} \]\[\text{2-Propanone (Acetone): } \text{CH}_3\text{COCH}_3 \] These are the only two structures that fit the formula with the required functional groups.

Identify Reaction with Oxidizing Agent

The question implies the oxidation of this unknown results in a compound that gives an acidic solution. Aldehydes, like 1-propanal, can be oxidized to acids, whereas ketones like 2-propanone are generally resistant to oxidation. Oxidizing 1-propanal forms propanoic acid, which is an acid and dissolves in water to give an acidic solution. This eliminates 2-propanone as the possible unknown compound.

Name the Oxidation Product

Upon oxidation, 1-propanal forms propanoic acid, a carboxylic acid known for giving acidic solutions in water. Thus, the name of the acid formed from oxidizing the unknown compound is propanoic acid.

Key concepts

Degree of Unsaturation

When trying to identify a carbonyl compound, understanding the degree of unsaturation is crucial. The degree of unsaturation, often denoted as \(d\), tells us how many rings or multiple bonds (like double or triple bonds) are present in the molecular structure. It is calculated with the formula: \(d = C + 1 - \frac{H + X - N}{2}\), where \(C\) is the number of carbon atoms, \(H\) is hydrogen, \(X\) represents halogens, and \(N\) is the count of nitrogen atoms.For the molecular formula \(\mathrm{C}_{3}\mathrm{H}_{6}\mathrm{O}\), the calculation simplifies to \(d = 3 + 1 - \frac{6}{2} = 2\), indicating two degrees of unsaturation. This usually suggests the presence of either two rings, two double bonds, or one of each. Knowing this information can significantly narrow down the possible structural choices for the compound.

Oxidizing Agent Reaction

Reacting a compound with an oxidizing agent can help in identifying carbonyl compounds. Oxidation is a process where the compound loses electrons, often resulting in the addition of oxygen or the removal of hydrogen in organic molecules, particularly in carbonyl groups. In the given exercise, the unknown compound reacted with an oxidizing agent to form an acid that dissolves in water to yield an acidic solution. This reaction is informative because aldehydes (like 1-propanal) readily oxidize to carboxylic acids. Ketones (such as 2-propanone), however, do not oxidize easily in mild conditions. Hence, the presence of an acidic solution after oxidation points towards an aldehyde, confirming that the unknown compound was 1-propanal.

Structural Isomers

Structural isomers are molecules with the same molecular formula but different structural arrangements of atoms. This means they can have different physical and chemical properties despite having the same counts of each type of atom.For the compound \(\mathrm{C}_{3}\mathrm{H}_{6}\mathrm{O}\), which has two degrees of unsaturation, there are two possible structures termed as isomers:

• 1-Propanal: \(\text{CH}_3\text{CH}_2\text{CHO}\)
• 2-Propanone (also known as Acetone): \(\text{CH}_3\text{COCH}_3\)

Both structures incorporate the same number of each atom type, yet their arrangements lead to different behaviors upon chemical reaction, as seen with their differing responses to oxidation.

Carbonyl Functional Groups

Carbonyl functional groups are characterized by a carbon atom double-bonded to an oxygen atom (\(C=O\)). These groups are highly reactive and are central to many chemical reactions, especially involving oxidation and reduction.In organic chemistry, carbonyls are found in various compounds, such as:

• Aldehydes: Where the carbonyl carbon is bonded to at least one hydrogen atom. Example: 1-Propanal.
• Ketones: Where the carbonyl carbon is bonded to two other carbon atoms. Example: 2-Propanone.

Understanding the behavior of carbonyl compounds involves observing their reactivity, particularly with oxidizing agents, as they can lead to further functional groups like carboxylic acids from aldehydes. This makes the identification and differentiation of aldehydes and ketones essential in organic synthesis.