Question

How many chiral carbons are in 2 -bromo-2-chloro-3-methylpentane? (a) 0, (b) 1. (c) 2, (d) 3, (e) 4 or more.

Short answer

The number of chiral carbons in 2-bromo-2-chloro-3-methylpentane is 1. The correct answer is (b) 1.

Step-by-step solution

Draw the structure of 2-bromo-2-chloro-3-methylpentane

We need to draw the structure of the given compound to visualize the molecule. To do this, we will arrange the substituents (bromo, chloro, and methyl) on the pentane chain as per the given IUPAC name. Here is the drawn structure: Br | H3C – C – H | | C – H Cl | H3C

Identify potential chiral carbons

Now, let's examine each carbon atom in the molecule to check if it is chiral. A carbon must be bound to four different substituents to be considered a chiral center. 1. The first carbon (leftmost) is bonded to three hydrogens and one carbon atom. It is not chiral. 2. The second carbon is bonded to a bromine, a chlorine, a hydrogen, and another carbon. It is a chiral carbon. 3. The third carbon is bonded to a methyl group, two hydrogens, and another carbon. It is not chiral. 4. The fourth carbon is bonded to three hydrogens and one carbon atom. It is not chiral. 5. The fifth carbon (rightmost) is bonded to three hydrogens and one carbon atom, and it is also not chiral.

Count the chiral carbons

Based on the analysis in Step 2, we've identified only one chiral carbon - the second carbon in the molecule. Therefore, the number of chiral carbons in 2-bromo-2-chloro-3-methylpentane is 1. The correct answer is (b) 1.

Key concepts

Organic Chemistry

Organic chemistry is the branch of chemistry that deals with the study of carbon-containing compounds. Carbon's ability to form four covalent bonds allows for a variety of complex structures, including chains, rings, and branches. This characteristic is what gives organic compounds their vast diversity. In the compound 2-bromo-2-chloro-3-methylpentane, we observe a carbon backbone termed a pentane chain because it consists of five carbon atoms.
The structuring and functional group placement in organic molecules directly influence the molecule's properties and reactivity. In our exercise, the organic backbone is modified with specific groups - bromo (Br) and chloro (Cl), which are considered halogens, and a methyl group (CH₃), which are common in organic molecules. These groups alter the molecule in significant ways, such as modifying its solubility, boiling point, and chemical reactivity.

Stereochemistry

Stereochemistry is the study of the spatial arrangement of atoms in molecules. This arrangement can greatly affect how a molecule behaves and interacts with other molecules. A key concept within stereochemistry is chirality. A chiral carbon atom is one that is bonded to four different substituents, allowing for two non-superimposable mirror images, similar to right and left hands.
In our exercise, identifying chiral carbons is essential. By analyzing the structure of 2-bromo-2-chloro-3-methylpentane, we identify that only the second carbon atom is chiral. This is because it is bonded to four different groups: bromine, chlorine, hydrogen, and another carbon. Understanding stereochemistry is crucial for predicting how molecules will interact with biological systems, as many biological molecules are also chiral.

IUPAC Nomenclature

IUPAC nomenclature is a standardized system for naming chemical compounds, ensuring that each name is unique and descriptive of the compound's structure. For organic compounds, the name typically consists of a prefix, infix, and suffix which describe the number of carbon atoms, types of bonds, and functional groups present.
In the compound 2-bromo-2-chloro-3-methylpentane, the name reveals key information about its structure. 'Pentane' indicates a five-carbon chain, while the prefixes 'bromo', 'chloro', and 'methyl' specify the location and type of substituents attached to this chain. The numbers (2 and 3) in the name indicate the exact carbon atoms to which these substituents are bonded. IUPAC nomenclature assists chemists worldwide in communicating complex information about molecular structure effectively.