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Which of the following IUPAC name is/are...

Which of the following `IUPAC` name is/are correct ?

A

B

C

D

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The correct Answer is:
To determine which of the given IUPAC names are correct, we need to analyze each name based on the rules of IUPAC nomenclature. Here’s a step-by-step solution: ### Step 1: Analyze the first name - 3-cyanobenzeneamide - The name suggests a benzene ring with a cyanide group (–C≡N) at the 3rd position and an amide group (–C(=O)NH2). - According to IUPAC rules, the correct name should reflect the presence of the amide group properly. - The correct name should be **3-cyanobenzenecarboxamide** instead of 3-cyanobenzeneamide. - **Conclusion**: This name is incorrect. **Hint**: Remember that when naming compounds with functional groups, the suffix should accurately reflect the functional group present. ### Step 2: Analyze the second name - The name suggests a benzene ring with a carbonyl chloride (–C(=O)Cl) group. - The carbonyl chloride is correctly named as it is a substituent on the benzene ring. - The name is correct as it follows the IUPAC naming conventions. **Hint**: Always check if the functional groups are named correctly and placed according to their priority. ### Step 3: Analyze the third name - The name indicates a phenyl ring with a carboxylate group. - The priority of the phenyl group is correctly noted, and the carboxylate group is properly represented. - This name is also correct. **Hint**: Ensure that the priority of substituents is considered when naming compounds with multiple functional groups. ### Step 4: Analyze the fourth name - 2-chloropropanoic ethanoisine hydride - This name suggests a propanoic acid derivative with a chloro substituent at the second position and an ethanoisine hydride. - The chloro substituent is correctly placed, and the name follows IUPAC rules. - This name is correct. **Hint**: Verify that the numbering of the carbon chain starts from the end closest to the highest priority functional group. ### Final Conclusion - The correct IUPAC names are: - **B**: Correct - **C**: Correct - **D**: Correct - **A**: Incorrect Thus, the correct answer is **B, C, and D**.

To determine which of the given IUPAC names are correct, we need to analyze each name based on the rules of IUPAC nomenclature. Here’s a step-by-step solution: ### Step 1: Analyze the first name - 3-cyanobenzeneamide - The name suggests a benzene ring with a cyanide group (–C≡N) at the 3rd position and an amide group (–C(=O)NH2). - According to IUPAC rules, the correct name should reflect the presence of the amide group properly. - The correct name should be **3-cyanobenzenecarboxamide** instead of 3-cyanobenzeneamide. - **Conclusion**: This name is incorrect. ...
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