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...
Related questions
Question
Give the structure of the major product (s) for the reaction listed below:

Transcribed Image Text:The image displays a chemical reaction involving an organic compound and a reagent. The compound is a cyclic structure, specifically cyclohexene, represented by a hexagon with one of the double bonds extending out to a methylene group (CH₂).
To the right of the compound, there is an arrow indicating the direction of the reaction. Above the arrow, the reagent NBS (N-bromosuccinimide) is written, and below the arrow, the symbol "hν" is present, indicating that the reaction requires light, typically involving ultraviolet (UV) light.
This setup suggests that the reaction shown is a bromination process under free radical conditions, commonly used to add bromine (Br) to the allylic position (adjacent to the double bond) of alkenes like cyclohexene. This kind of reaction is useful in organic synthesis for introducing functionality into hydrocarbon structures.
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