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...
Related questions
Question
![Draw all resonance structures of the ion shown here and
determine which is the strongest contributor to its
resonance hybrid.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F3a955612-da34-4a24-bb6a-cb9107adde3f%2Fa71ce690-8ee4-4245-9f9a-c58f24ed78ec%2F8wsbbf7.png&w=3840&q=75)
Transcribed Image Text:Draw all resonance structures of the ion shown here and
determine which is the strongest contributor to its
resonance hybrid.
Expert Solution
![](/static/compass_v2/shared-icons/check-mark.png)
Step 1
Carbocation-
These are formed by carbon by loss of one electron. They are act as electron deficient species that is electrophiles. As carbon is electron deficient they can attract electrons easily. Carbocation has greater act of alkyl substitution. Carbocation in allylic position are more stable. Carbocation intermediates stability in the order as shown as below-
30>20>10
Step 2
Answer of given question:
Resonance structures of given structure:
Here (C) is strongest contributor to its resonance since it is 30 carbocation.
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