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The correct IUPAC name for the following compound is:

The correct IUPAC name for the following compound is:

Chemistry
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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**Question 5** The correct IUPAC name for the following compound is: [Image shows a molecular structure with a double bond and substituents: Bromine (Br) attached to carbon in a double-bonded area, and Chlorine (Cl) as another substituent further away on the chain. There are branches off the main carbon chain.] **Options:** - (E)-2-Methyl-5-bromo-4-chloro-4-hexene - (E)-2-Bromo-3-chloro-5-methyl-3-hexene - (Z)-2-Bromo-3-chloro-5-methyl-3-hexene - (Z)-2-Bromo-3-chloro-5-methyl-2-hexene - (E)-2-Bromo-3-chloro-5-methyl-2-hexene **Diagram Explanation:** The diagram represents a hydrocarbon chain featuring a halogenated substitute with a double bond, indicating possible stereochemistry (E/Z). The specific locations of Br and Cl, along with the double bond, need to be analyzed to determine the proper IUPAC name. Be sure to consider the longest carbon chain, the position of each substituent, and the stereochemical descriptor (E/Z).
Transcribed Image Text:**Question 5** The correct IUPAC name for the following compound is: [Image shows a molecular structure with a double bond and substituents: Bromine (Br) attached to carbon in a double-bonded area, and Chlorine (Cl) as another substituent further away on the chain. There are branches off the main carbon chain.] **Options:** - (E)-2-Methyl-5-bromo-4-chloro-4-hexene - (E)-2-Bromo-3-chloro-5-methyl-3-hexene - (Z)-2-Bromo-3-chloro-5-methyl-3-hexene - (Z)-2-Bromo-3-chloro-5-methyl-2-hexene - (E)-2-Bromo-3-chloro-5-methyl-2-hexene **Diagram Explanation:** The diagram represents a hydrocarbon chain featuring a halogenated substitute with a double bond, indicating possible stereochemistry (E/Z). The specific locations of Br and Cl, along with the double bond, need to be analyzed to determine the proper IUPAC name. Be sure to consider the longest carbon chain, the position of each substituent, and the stereochemical descriptor (E/Z).
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