Name each disubstituted benzene. b.

Verified step by step guidance

Identify the parent structure, which is benzene.

Determine the substituents attached to the benzene ring. In this case, there are two chlorine (Cl) atoms.

Number the carbon atoms in the benzene ring such that the substituents get the lowest possible numbers. Start numbering from one of the carbons with a chlorine atom.

Assign the positions of the chlorine atoms. For example, if the chlorines are on adjacent carbons, they are in the 1,2-positions.

Combine the position numbers with the substituent names and the parent structure to form the name. For instance, if the chlorines are in the 1,2-positions, the name would be 1,2-dichlorobenzene.

Verified video answer for a similar problem:

This video solution was recommended by our tutors as helpful for the problem above.

Video duration:

Was this helpful?

Key Concepts

Here are the essential concepts you must grasp in order to answer the question correctly.

Disubstituted Benzene

Disubstituted benzene refers to a benzene ring that has two substituents attached to it. The position of these substituents can significantly affect the chemical properties and reactivity of the compound. The naming of disubstituted benzenes follows specific rules based on the relative positions of the substituents, which can be ortho (adjacent), meta (one carbon apart), or para (opposite sides).

Nomenclature of Aromatic Compounds

The nomenclature of aromatic compounds, particularly disubstituted benzenes, is governed by the IUPAC naming conventions. The substituents are named in alphabetical order, and the positions are indicated by numbers based on the carbon atoms of the benzene ring. For example, in the case of two chlorine substituents, the compound can be named as 1,2-dichlorobenzene (ortho), 1,3-dichlorobenzene (meta), or 1,4-dichlorobenzene (para) depending on their positions.

Electrophilic Aromatic Substitution

Electrophilic aromatic substitution is a fundamental reaction mechanism in organic chemistry where an electrophile replaces a hydrogen atom on an aromatic ring. This process is crucial for understanding how substituents can influence the reactivity of the benzene ring. The presence of electron-withdrawing groups, like chlorine, can direct incoming electrophiles to specific positions on the ring, affecting the overall structure and properties of the resulting disubstituted benzene.