**Chemical Reaction with N-Bromosuccinimide (NBS):** The compound shown is treated with N-bromosuccinimide (NBS) in the presence of light.**Description of Reaction:**1. **Structure of the Compound:** The compound depicted is a bicyclic alkene with substituents.2. **Task Requirement:** Draw both resonance structures for the radical produced by the reaction of the compound with a bromine atom. The assumption is made that the reaction occurs only at the weakest C-H bond.**Diagrams/Graphs:** - There are no additional graphs or diagrams provided. This exercise focuses on understanding the radical formation and resonance stabilization during the bromination process using NBS, a common reaction in organic chemistry for allylic bromination.

-> Given, NBS⇒ N-b nomo succinimide

The compound below is treated with N-bromosuccinimide (NBS) in the presence of light. Draw both resonance structures for the radical produced by reaction of the compound with a bromine atom. Assume reaction occurs only at the weakest C-H bond.

The compound below is treated with N-bromosuccinimide (NBS) in the presence of light. Draw both resonance structures for the radical produced by reaction of the compound with a bromine atom. Assume reaction occurs only at the weakest C-H bond.

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...

See similar textbooks

Related questions

Q: How these electrons move in forming and breaking bonds, and if a reaction proceeds via a radical or…

A: The formation of a bond takes place by either sharing of electrons or by complete transfer of…

Q: resonance and inductive effects if present.

A: Both phenol and benzene are nucleophilic in nature due to different reasons. Both, inductive and…

Q: Aromatic compounds which contain non-carbon atoms (e.g., O, N, S) as part of the cyclic conjugated a…

A: 1.) there is only 1 lone pair on oxygen atom (because 1 lone pair gets involved in resonance so…

Q: Draw the four resonance structures for anthracene.

A: Resonance structures differ only in the position of lone pair or its pie electrons. The position of…

Q: II :ZI

Q: Br from 1-bromo-2-methylpropane HO X

A: Answer:- The question is based on the concept of organic synthesis. we need to synthesize the…

Q: Free‑radical halogenation can occur with chlorine and a source of direct UV radiation or sunlight.…

A: The relative reactivities of the three types of hydrogen atoms to substitution by Cl are 1°:2°:3° =…

Q: Predict the organic product of the reaction. Include all hydrogen atoms

A: In the presence of sulfuric acid, alkene undergoes to hydration to produce alcohol. The kinetic of…

Q: The ethylation of benzene is an electrophilic substitution reaction. Identify the electrophile in…

Q: 4) Which nitrogen atom in the structure below is most nucleophilic? Please explain by discussing the…

A: Given is organic compound.Nucleophiles are either negatively charged or neutral species with lone…

Q: 4-Methylphenol is more acidic than ethanol (pKa 10.36 vs 16.0) , even though both contain an OH…

A: The organic compounds containing -OH group are slightly acidic in nature. The acidic properties of…

Q: Draw all of the intermediate resonance structures that would occur if bromine added to anisole. Draw…

Q: II IV III

Q: how many structurally isomeric products form in the free radical bromination of hexane?

A: Free radical bromination of hexane is a reaction in which the hexane molecule will react with Br2…

Q: How is sodium enolate formed by adding NaOH to dimedone? What is the structure? Please include the…

A: Dimedone is a cyclic diketone, which means it has two carbonyl groups (C=O) in a six-membered ring.…

Q: Please explain Frost Circles for aromatic systems and how they can be used to explain the stability…

A: A question to describe about Frost circles for aromatic systems.

Concept explainers

UV Visible Spectroscopy

Spectroscopy refers to the absorption or emission of light or other radiations by matter. When a substance or chemical absorbs light or radiation, they reach an excited state followed by de-excitation or emission of the light or radiation forming distinct spectra. UV-visible spectroscopy or ultraviolet-visible refers to the absorption and emission in the ultraviolet and visible regions of the electromagnetic spectrum.

Question

**Chemical Reaction with N-Bromosuccinimide (NBS):**
The compound shown is treated with N-bromosuccinimide (NBS) in the presence of light.

**Description of Reaction:**

1. **Structure of the Compound:**
The compound depicted is a bicyclic alkene with substituents.

2. **Task Requirement:**
Draw both resonance structures for the radical produced by the reaction of the compound with a bromine atom. The assumption is made that the reaction occurs only at the weakest C-H bond.

**Diagrams/Graphs:**
- There are no additional graphs or diagrams provided.

This exercise focuses on understanding the radical formation and resonance stabilization during the bromination process using NBS, a common reaction in organic chemistry for allylic bromination.

Expert Solution

This question has been solved!

Explore an expertly crafted, step-by-step solution for a thorough understanding of key concepts.

This is a popular solution!

SEE SOLUTION Check out a sample Q&A here

Step 1

VIEW

Step 2

VIEW

Step 3

VIEW

Trending now

This is a popular solution!

Step by step

Solved in 3 steps with 4 images

SEE SOLUTION Check out a sample Q&A here

Knowledge Booster

Learn more about

Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.

Similar questions

For the following compounds answer part a and b.
Using the concept of resonance, explain why the nitro group deactivates electrophilic aromatic substitution reactions, but facilitates nucleophilic aromatic substitution reactions.
Consider the fluorination and bromination of methane by the free radical mechanism.Making use of bond energies discuss the thermodynamic favorability (free energy change) of the two reactions.
How do you write out the reactions (reactants, conditions and products) for the following electrophilic aromatic substitution reactions Bromination of methylbenzoate Nitration of anisole (methoxybenzene) Bromination of anisole (methoxybenzene)
Draw resonance structures for the conjugate base that is produced when the following compound is treated with sodium ethoxide. منة OEt There are THREE significant resonance structures for the conjugate base of this compound. Modify the given copies of the original compound to draw the resonance structures (no curved arrows are needed, and lone pairs do not have to be drawn). Use the +/- tools to add/remove charges, and use the single bond tool to interconvert between double and single bonds. H3C H3C H3C Edit Drawing CH3 CH3 CH3
The dehydration of compound A produces many different products. One of the products formed is compound G. Can you figure out the mechanism? The mechanism proceeds through five intermediates (compounds B-F). Sort the intermediates according to the reaction mechanism which includes a methyl shift, a hydride shift and a resonance structure. Note: treat resonance structures as individual steps. Compound III Compound IV Compound II Compound I Compound V Your answer compound A OH compound G intermediates II
Draw both resonance structures of the anion formed by the reaction of the most acidic C-H bond of the compounds below with base.
Phenol (hydroxybenzene) behaves as a weak acid. a) Write out the equilibrium equation for its partial dissociation in water. b) Write out the expression for the acid dissociation constant, Ka. d) Draw the conjugate base of phenol and show how it is stabilised by resonance. e) Compare and explain the acidity of phenol (p = 9.9) with that of: cyclohexanol (pk = 16.0) 3-fluorophenol (pK₁ = 9.3) 4-acetylphenol (pK, = 8.1)
eq eq M M M ereg 2req 2req 2req X 2req J F3 $ 4 R C V [Review Topics] [References] Draw both resonance structures of the anion formed by the reaction of the most acidic C-H bond of the compound below with base. 4x Include all valence lone pairs in your answer. • For structures having different hydrogens of comparable acidity, assume that the reaction occurs at the less-substituted carbon. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate resonance structures using the symbol from the drop-down menu. ✓✓99.81 O 0- F4 . % 5 T G B F5 *** ^ 6 Cengage Learning Cengage Technical Support Y ChemDoodle H N F6 & N& 7 U O J F7 + [ ] در M 8 PrtScn K F8 9 Home O 83°F Sunny F9 L ) 0 End F10 P Previous C PgUp F11 9 ? Next Save and Exit 9:38 AM 7/18/2022 PgDn F12 0 Ins D Back