correct IUPAC name

Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Provide the correct IUPAC name
The image presents a chemistry question, asking for the correct IUPAC name of a compound. The compound is displayed with a structural formula that includes a bromine (Br) atom attached to a carbon chain, along with a carboxylic acid functional group (COOH).

### Key Features of the Compound:
- **Bromine (Br) Atom:** Located on the second carbon of the chain.
- **Carboxylic Acid Group:** Positioned at the end of the carbon chain.

### Diagram Details:
- The main carbon chain is unsaturated, indicating single bonds between carbons.
- The bromine atom creates a point of differentiation in the chain, suggesting a substituent naming in the IUPAC nomenclature.

### Interactive Choice Options:
Below the structural diagram, several interactive button elements are provided. These include:

#### Numbers:
- 7-, 5-, 2-, 4-, 3-, 6-

#### Prefixes:
- iso, di, tri, sec-, tert-, bromo-

#### Suffixes and Root Words:
- boro, pent, yl, but, prop, meth

These elements likely serve as parts to construct the IUPAC name, allowing a combination of numbers and prefixes/suffixes to create the proper chemical nomenclature. The correct construction should consider the principal carbon chain length and substituent positions.
Transcribed Image Text:The image presents a chemistry question, asking for the correct IUPAC name of a compound. The compound is displayed with a structural formula that includes a bromine (Br) atom attached to a carbon chain, along with a carboxylic acid functional group (COOH). ### Key Features of the Compound: - **Bromine (Br) Atom:** Located on the second carbon of the chain. - **Carboxylic Acid Group:** Positioned at the end of the carbon chain. ### Diagram Details: - The main carbon chain is unsaturated, indicating single bonds between carbons. - The bromine atom creates a point of differentiation in the chain, suggesting a substituent naming in the IUPAC nomenclature. ### Interactive Choice Options: Below the structural diagram, several interactive button elements are provided. These include: #### Numbers: - 7-, 5-, 2-, 4-, 3-, 6- #### Prefixes: - iso, di, tri, sec-, tert-, bromo- #### Suffixes and Root Words: - boro, pent, yl, but, prop, meth These elements likely serve as parts to construct the IUPAC name, allowing a combination of numbers and prefixes/suffixes to create the proper chemical nomenclature. The correct construction should consider the principal carbon chain length and substituent positions.
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