To illustrate the stabilization of a carboxylate anion, the resonance structure and resonance hybrid structure of the carboxylate ion are to be drawn. Concept introduction: Resonance exists in species for which there are two or more valid Lewis structures. Resonance structures differ only in the placement of their valence electrons, not their atoms. Resonance structures are imaginary; the one, true species is represented by the resonance hybrid. A resonance hybrid is a weighted average of all resonance structures. Resonance provides stabilization. The resonance hybrid looks most like the most stable resonance structure. Resonance stabilization is usually large when resonance structures are equivalent.

Question

Want to see the full answer?

Answer 1

Question

Chapter 20, Problem 20.7YT

Interpretation Introduction

Interpretation:

To illustrate the stabilization of a carboxylate anion, the resonance structure and resonance hybrid structure of the carboxylate ion are to be drawn.

Concept introduction:

Resonance exists in species for which there are two or more valid Lewis structures. Resonance structures differ only in the placement of their valence electrons, not their atoms. Resonance structures are imaginary; the one, true species is represented by the resonance hybrid. A resonance hybrid is a weighted average of all resonance structures. Resonance provides stabilization. The resonance hybrid looks most like the most stable resonance structure. Resonance stabilization is usually large when resonance structures are equivalent.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

Protecting Groups and Carbonyls 6) The synthesis generates allethrolone that exhibits high insect toxicity but low mammalian toxicity. They are used in pet shampoo, human lice shampoo, and industrial sprays for insects and mosquitos. Propose detailed mechanistic steps to generate the allethrolone label the different types of reagents (Grignard, acid/base protonation, acid/base deprotonation, reduction, oxidation, witting, aldol condensation, Robinson annulation, etc.) III + VI HS HS H+ CH,CH,Li III I II IV CI + P(Ph)3 V ༼ Hint: no strong base added VI S VII IX HO VIII -MgBr HgCl2,HgO HO. isomerization aqeuous solution H,SO, ༽༽༤༽༽ X MeOH Hint: enhances selectivity for reaction at the S X ☑

Draw the complete mechanism for the acid-catalyzed hydration of this alkene. esc 田 Explanation Check 1 888 Q A slock Add/Remove step Q F4 F5 F6 A བྲA F7 $ % 5 @ 4 2 3 & 6 87 Click and drag to start drawing a structure. © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Ce W E R T Y U S D LL G H IK DD 요 F8 F9 F10 F1 * ( 8 9 0 O P J K L Z X C V B N M H He command

Explanation Check F1 H₂O H₂ Pd 1) MCPBA 2) H3O+ 1) Hg(OAc)2, H₂O 2) NaBH4 OH CI OH OH OH hydration halohydrin formation addition halogenation hydrogenation inhalation hydrogenation hydration ☐ halohydrin formation addition halogenation formation chelation hydrogenation halohydrin formation substitution hydration halogenation addition Ohalohydrin formation subtraction halogenation addition hydrogenation hydration F2 80 F3 σ F4 F5 F6 1 ! 2 # 3 $ 4 % 05 Q W & Å © 2025 McGraw Hill LLC. All Rights Reserved. F7 F8 ( 6 7 8 9 LU E R T Y U A F9