hydrogen by the resonance and the inductive mechanisms. a = acceptor d = donor n = no effect :0: 1. 2. 3. :0: -N(CH3)2 ——CH,CH,CH,N(CH3)2 Ö: -S-CH3 Inductive effect Inductive effect Inductive effect Resonance effect Resonance effect Resonance effect

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...
icon
Related questions
Question
**Classify the following substituents according to whether they are electron donors or electron acceptors relative to hydrogen by the resonance and the inductive mechanisms.**

- **a = acceptor**
- **d = donor**
- **n = no effect**

1. **Structure:** Benzene ring with \(\text{-N(CH}_3\text{)}_2\) substituent.
   - **Inductive effect:** [ ]
   - **Resonance effect:** [ ]

2. **Structure:** Benzene ring with \(\text{-CH}_2\text{CH}_2\text{CH}_2\text{N(CH}_3\text{)}_2\) substituent.
   - **Inductive effect:** [ ]
   - **Resonance effect:** [ ]

3. **Structure:** Methanesulfonyl group \((\text{-S(=O)}_2\text{CH}_3)\).
   - **Inductive effect:** [ ]
   - **Resonance effect:** [ ]
Transcribed Image Text:**Classify the following substituents according to whether they are electron donors or electron acceptors relative to hydrogen by the resonance and the inductive mechanisms.** - **a = acceptor** - **d = donor** - **n = no effect** 1. **Structure:** Benzene ring with \(\text{-N(CH}_3\text{)}_2\) substituent. - **Inductive effect:** [ ] - **Resonance effect:** [ ] 2. **Structure:** Benzene ring with \(\text{-CH}_2\text{CH}_2\text{CH}_2\text{N(CH}_3\text{)}_2\) substituent. - **Inductive effect:** [ ] - **Resonance effect:** [ ] 3. **Structure:** Methanesulfonyl group \((\text{-S(=O)}_2\text{CH}_3)\). - **Inductive effect:** [ ] - **Resonance effect:** [ ]
Expert Solution
Step 1: Resonance and inductive effect

The inductive effect mainly arises when there is a difference in electronegativity values of the bonded atom. The more electronegative atom withdraws the electron density from the bond, which leads to a permanent polarization in the compound. This is transmitted along the sigma (σ) bonds.

Resonance involves the delocalization of pi or lone pair electrons which are in conjugation.  The groups that withdraw electron density are called -R groups and those that donate electron density are called +R groups.


steps

Step by step

Solved in 3 steps

Blurred answer
Knowledge Booster
Mass Spectrometry
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.
Recommended textbooks for you
Chemistry
Chemistry
Chemistry
ISBN:
9781305957404
Author:
Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:
Cengage Learning
Chemistry
Chemistry
Chemistry
ISBN:
9781259911156
Author:
Raymond Chang Dr., Jason Overby Professor
Publisher:
McGraw-Hill Education
Principles of Instrumental Analysis
Principles of Instrumental Analysis
Chemistry
ISBN:
9781305577213
Author:
Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:
Cengage Learning
Organic Chemistry
Organic Chemistry
Chemistry
ISBN:
9780078021558
Author:
Janice Gorzynski Smith Dr.
Publisher:
McGraw-Hill Education
Chemistry: Principles and Reactions
Chemistry: Principles and Reactions
Chemistry
ISBN:
9781305079373
Author:
William L. Masterton, Cecile N. Hurley
Publisher:
Cengage Learning
Elementary Principles of Chemical Processes, Bind…
Elementary Principles of Chemical Processes, Bind…
Chemistry
ISBN:
9781118431221
Author:
Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:
WILEY