Start with a cyclohexane. Add double bonds at the 1st, 3rd and 5th carbons. Add an OH group somewhere on the ring. Fill the empty carbons with iodines so that they are in positions 2 and 4 on the ring. Name:t. Start with a cyclohexane.Add double bonds at the 1t. 3rd, and 5th carbons.Add an OH group somewhere on the ring.Fill the empty carbons with iodines so that they are inpositions 2 and 4 on the ring.Name:

Start with a cyclohexane. Add double bonds at the 1st, 3rd and 5th carbons. Add an OH group somewhere on the ring. Fill the empty carbons with iodines so that they are in positions 2 and 4 on the ring.

Start with a cyclohexane. Add double bonds at the 1st, 3rd and 5th carbons. Add an OH group somewhere on the ring. Fill the empty carbons with iodines so that they are in positions 2 and 4 on the ring.

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

ChapterNW2: Nomenclature Worksheet 2: Intro To Naming Functional Groups

Section: Chapter Questions

Problem 18CTQ

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Question

Name:
t. Start with a cyclohexane.
Add double bonds at the 1t. 3rd, and 5th carbons.
Add an OH group somewhere on the ring.
Fill the empty carbons with iodines so that they are in
positions 2 and 4 on the ring.
Name:

Expert Solution

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The name of the structure would be 2,4-diiodophenol

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