Aldehydes and ketones that have a hydrogen atom at the alpha position can be converted into a carbanion in the presence of a base as follows. This source of the stability of this carbanion is -H2 gas H polar interaction between the negative charge and the partial positive charges in the solvent O delocalization of the negative charge to the adjacent carbonyl group O the electron donating effect of the alpha carbon the electron withdrawing effect of the alpha carbon
Aldehydes and ketones that have a hydrogen atom at the alpha position can be converted into a carbanion in the presence of a base as follows. This source of the stability of this carbanion is -H2 gas H polar interaction between the negative charge and the partial positive charges in the solvent O delocalization of the negative charge to the adjacent carbonyl group O the electron donating effect of the alpha carbon the electron withdrawing effect of the alpha carbon
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...
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![Aldehydes and ketones that have a hydrogen atom at the alpha position can be
converted into a carbanion in the presence of a base as follows. This source of
the stability of this carbanion is
-H2 gas
+
polar interaction between the negative charge and the partial positive charges in the
solvent
O delocalization of the negative charge to the adjacent carbonyl group
the electron donating effect of the alpha carbon
the electron withdrawing effect of the alpha carbon](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F6c8de15a-811f-456b-b916-24ec263405f4%2Feeeb6ae5-c8ff-40df-bc1e-f3df19a3082c%2Fwxh36p8_processed.jpeg&w=3840&q=75)
Transcribed Image Text:Aldehydes and ketones that have a hydrogen atom at the alpha position can be
converted into a carbanion in the presence of a base as follows. This source of
the stability of this carbanion is
-H2 gas
+
polar interaction between the negative charge and the partial positive charges in the
solvent
O delocalization of the negative charge to the adjacent carbonyl group
the electron donating effect of the alpha carbon
the electron withdrawing effect of the alpha carbon
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