Learning Path
Question & Answer1
Understand Question2
Review Options3
Learn Explanation4
Explore TopicChoose the Best Answer
A
1-bromo-3-ethylcyclohexane
B
3-bromo-1-ethylcyclohexane
C
1-ethyl-3-bromocyclohexane
D
3-ethyl-1-bromocyclohexane
Understanding the Answer
Let's break down why this is correct
Answer
The correct IUPAC name is 1‑bromo‑3‑ethylcyclohexane. First, choose a numbering that gives the lowest possible locants for the substituents; starting at the bromine gives locants 1 and 3, which is lower than the alternative 1 and 4 that would arise if you started at the ethyl group. The prefix “bromo” comes before “ethyl” because halogens have higher alphabetical priority. Thus the full name is 1‑bromo‑3‑ethylcyclohexane. For example, a molecule with a bromine on carbon 1 and an ethyl group on carbon 3 of the cyclohexane ring is described by that name.
Detailed Explanation
The IUPAC rule orders substituents alphabetically, not by their locants. Other options are incorrect because Some students think the substituent with the lowest locant should be listed first; This option reverses the alphabetical order.
Key Concepts
Substituent Identification
Topic
Cycloalkanes Naming
Difficulty
easy level question
Cognitive Level
understand
Practice Similar Questions
Test your understanding with related questions
1
Question 1A team of chemists is developing a new drug that involves a cyclohexane ring structure with multiple substituents. They need to name their compound correctly to ensure clarity in communication and research. If one substituent is a methyl group and another is a hydroxyl group, while the hydroxyl group is positioned at carbon 1 and the methyl group at carbon 3, what is the correct IUPAC name for the compound?
hardChemistry
Practice
2
Question 2Which of the following is the correct name for a cyclohexane with one methyl group at position 1 and a bromine at position 3?
mediumChemistry
Practice
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