Question

Anthracene (mp \(217^{\circ}\) ) forms a red crystalline complex (mp \(164^{\circ}\) ) with 1,3,5-trinitrobenzene (mp \(121^{\circ}\) ). If you were to purify anthracene as this complex, how could you regenerate the anthracene free of trinitrobenzene?

Short answer

Dissolve the complex, crystallize anthracene, and filter to separate it.

Step-by-step solution

Understanding the Complex Formation

The task involves purifying anthracene by forming a complex with 1,3,5-trinitrobenzene. This complex has a lower melting point than that of pure anthracene or 1,3,5-trinitrobenzene, indicating a stable association between the two molecules.

Dissolve the Complex

Dissolve the red crystalline complex in a suitable solvent (e.g., ethanol or dichloromethane) to break the associative bonds between anthracene and 1,3,5-trinitrobenzene. Choose a solvent in which both components have different solubilities.

Selective Crystallization

Use the difference in solubility or crystallization properties to separate anthracene from 1,3,5-trinitrobenzene. Cool the solution slowly, allowing anthracene, which has a higher tendency to crystallize out due to its lower solubility in typical organic solvents, to precipitate first.

Filtration of Pure Anthracene

Filter the solid out of the solution. The precipitate should predominantly contain anthracene because it crystallizes out first at its melting point of 217°C, which is higher than that of the complex.

Remove Solvent and Trinitrobenzene

Evaporate any remaining solvent and keep 1,3,5-trinitrobenzene dissolved. Ensuring complete drying will help in obtaining anthracene with no residual trinitrobenzene.

Verification of Purity (Optional)

Verify the purity of the recovered anthracene by measuring its melting point. It should match the pure material’s melting point of 217°C. Deviations may indicate contaminations or incomplete removal of trinitrobenzene.

Key concepts

Purification Techniques

In organic chemistry, purification techniques are crucial for obtaining substances in their pure form, key for reaction accuracy and product quality. One common method involves creating a compound complex. This technique takes advantage of the physical properties of molecular complexes, such as melting points.
When anthracene forms a complex with 1,3,5-trinitrobenzene, it results in a stable mixture with a distinct melting point. By focusing on these properties, chemists can isolate and purify compounds effectively. Dissolution of the complex in a solvent like ethanol enables separation by exploiting differences in solubility.

• Solvent choice is vital, based on how each component dissolves.
• The goal is to break apart the complex to retrieve pure substances.

Mastering such techniques can significantly improve the efficiency of purifying organic compounds in a laboratory setting.

Complex Formation

Complex formation is a phenomenon where two or more compounds associate, forming a new entity with unique physical or chemical properties. In the case of anthracene, forming a complex with 1,3,5-trinitrobenzene stabilizes the structure.
This association often results in altered melting points and solubility, which can be leveraged for purification. For instance, the red crystalline complex observed has a lower melting point than its components, showing a tight intermolecular interaction.

• These complexes can be reversible, allowing for separation procedures.
• Understanding the interaction between molecules aids in effectively controlling such formations.

Through precise manipulation, chemists can separate compounds post-formation, returning anthracene to its pure state.

Solubility and Crystallization

One of the key principles in separating and purifying compounds is using solubility and crystallization. Differences in solubility are harnessed by dissolving the complex in a solvent where each component has different solubility limits.
Crystallization involves cooling the solution slowly, promoting the less soluble substance to form crystals first. In purifying anthracene from its complex, anthracene will crystallize out first because its solubility is lower relative to 1,3,5-trinitrobenzene in many solvents.

• The careful control of temperature aids in crystal formation.
• This technique ensures anthracene is collected with minimal impurities.

Through controlling these physical properties, pure substances can be isolated from complex mixtures.

Melting Point Analysis

Melting point analysis is a definitive test for verifying the purity of a compound. Pure substances have precise melting points, and any deviations can indicate the presence of impurities.
In purifying anthracene, a final examination involves checking its melting point against the known standard of 217°C. If variations exist, it suggests remaining impurities like traces of trinitrobenzene.

• This analysis serves as a quality check post purification.
• Consistency in melting confirms the success of the separation process.

Ensuring accurate melting point results is essential for confirming the integrity of the purified compound.