The resonance structures for each of the given compounds are to be written. Concept introduction: In the conjugated systems, conjugation is the interaction of p -orbitals with one another across an intervening sigma bond. A conjugated system, in simple words, can be represented as a system in which compounds have alternate double bonds and single bonds. The delocalization of unpaired electrons results in the increase of stability of the primary, secondary, and tertiary carbocations. Resonance is defined as the movement of pi-electrons from one carbon to another in order to stabilize the charged intermediates. Having a higher resonance or more resonant structures means more stability. Resonant structures do not actually exist on their own. It is a study of the mechanism for the formation of an organic compounds. Only electrons can be moved while writing resonance structures. All structures should be in proper Lewis structures. All resonance structures should have the same number of unpaired electrons. All atoms that contribute in the delocalized π -electron system must lie in or near the plane.

Question

Want to see the full answer?

Answer 1

Question

Chapter 13, Problem 3PP

Interpretation Introduction

Interpretation:

The resonance structures for each of the given compounds are to be written.

Concept introduction:

In the conjugated systems, conjugation is the interaction of p-orbitals with one another across an intervening sigma bond.

A conjugated system, in simple words, can be represented as a system in which compounds have alternate double bonds and single bonds.

The delocalization of unpaired electrons results in the increase of stability of the primary, secondary, and tertiary carbocations.

Resonance is defined as the movement of pi-electrons from one carbon to another in order to stabilize the charged intermediates.

Having a higher resonance or more resonant structures means more stability.

Resonant structures do not actually exist on their own. It is a study of the mechanism for the formation of an organic compounds.

Only electrons can be moved while writing resonance structures.

All structures should be in proper Lewis structures.

All resonance structures should have the same number of unpaired electrons.

All atoms that contribute in the delocalized π-electron system must lie in or near the plane.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

For each reaction below, decide if the first stable organic product that forms in solution will create a new CC bond, and check the appropriate box. Next, for each reaction to which you answered "Yes" to in the table, draw this product in the drawing area below. Note for advanced students: for this problem, don't worry if you think this product will continue to react under the current conditions - just focus on the first stable product you expect to form in solution. ? Will the first MgBr product that forms in this reaction create a new CC bond? olo ? OH جمله O Yes Ⓒ No MgCl ? Will the first product that forms in this reaction create a new CC bond? Click and drag to start drawing a structure. Yes No X ☐ : ☐ टे PH

Assign all the protons

PROPOSE REACTION MECHANISM FOR ACID-CATALYZED REACTION OF 3-PENTANONE WITH DIMETHYLAMINE