### Question:Which of the following compounds is much better monohalogenated in the presence of light with N-bromosuccinimide (NBS) rather than elemental bromine (Br₂)?### Answer Choices:(A)![A](/path/to/image_a.png)(B)![B](/path/to/image_b.png)(C)![C](/path/to/image_c.png)(D)![D](/path/to/image_d.png)### Details of the Structures:- **Option (A)**: The compound is a hexagon with one double bond, indicating it is a cyclohexene.- **Option (B)**: The compound is CH₄, which is methane.- **Option (C)**: The compound shows isobutane structure.- **Option (D)**: The compound is a cyclopentane, a pentagon structure.### Explanation:N-bromosuccinimide (NBS) is commonly used for brominating compounds at allylic positions (adjacent to double bonds) in the presence of light. Elemental bromine (Br₂) can also be used for bromination but is less selective. Therefore, the choice involves understanding the specific conditions where NBS is more efficient.#### Graphs or Diagrams:Currently, there are no graphs or diagrams provided other than the structural representations of the compounds. ### Correct Choice:The compound given in **Option (A)**, cyclohexene, is more likely to be monohalogenated with NBS under the given conditions due to the presence of a double bond that favors allylic bromination.

Given statement is : Options are :

Answered: Which of the following compounds is…

Which of the following compounds is much better monohalogenated in the presence of light with N-bromosuccinimide (NBS) rather than elemental bromine (Br₂)? CH4 (B) (A) (D)

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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Concept explainers

Organomagnesium compounds

The interaction of alkyl halide with Mg metal in a suitable ether solvent is the common method for the synthesis of the Grignard reagent.

Hydrolysis Grignard Reactions and Reduction

Organomagnesium halides are Grignard reagents. Francois Auguste Victor Grignard, a French chemist who received the Nobel Prize in Chemistry in 1912, created these highly useful reagents.

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