The structure shown below is has a very high pka because the conjugate base is very unstable. Using the provided resonance structures, draw the curved electron-pushing arrows to show the deprotonation step. Then, draw the curved electron-pushing arrows to show the interconversion between resonance hybrid contributors. Be sure to account for all bond- breaking and bond-making steps. Drawing Arrows CH3CH2CH2CH2Li Li Ⓒ T + 4 H E H H

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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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The structure shown below is has a very high pka
because the conjugate base is very unstable. Using
the provided resonance structures, draw the
curved electron-pushing arrows to show the
deprotonation step. Then, draw the curved
electron-pushing arrows to show the
interconversion between resonance hybrid
contributors. Be sure to account for all bond-
breaking and bond-making steps.
Drawing Arrows
CH3CH2CH2CH2Li
Hac:O
C: 0
+
H
Undo
H
H
W
Reset
H
Done
H
Transcribed Image Text:The structure shown below is has a very high pka because the conjugate base is very unstable. Using the provided resonance structures, draw the curved electron-pushing arrows to show the deprotonation step. Then, draw the curved electron-pushing arrows to show the interconversion between resonance hybrid contributors. Be sure to account for all bond- breaking and bond-making steps. Drawing Arrows CH3CH2CH2CH2Li Hac:O C: 0 + H Undo H H W Reset H Done H
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