Answer the following questions for the reaction scheme below:phenolpka - 10.0OHCENcyanidaa. The equilibrium favors the [Select]phenolate99b. This reaction is best described as a(n) [Selectc. The strongest acid in the reaction is the [Select]d. The nucleophile in the forward reaction is [Select]e The electrophile in the reverse reaction is [Select]!!HTC=Nhydrogen cyanidepka - 3.46reaction.>hp

The equilibrium reaction given is

Answer the following questions for the reaction scheme below: phenol pka-10.0 OH CEN cyanida a. The equilibrium favors the [Select] phenolate b. This reaction is best described as a(n) [Select] + HIC N c. The strongest acid in the reaction is the [Select] d. The nucleophile in the forward reaction is [Select] e The electrophile in the reverse reaction is [Select] hydrogen cyanide pka - 3.46 reaction. <

Answer the following questions for the reaction scheme below: phenol pka-10.0 OH CEN cyanida a. The equilibrium favors the [Select] phenolate b. This reaction is best described as a(n) [Select] + HIC N c. The strongest acid in the reaction is the [Select] d. The nucleophile in the forward reaction is [Select] e The electrophile in the reverse reaction is [Select] hydrogen cyanide pka - 3.46 reaction. <

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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Answer the following questions for the reaction scheme below: OH e :CEN HIC N cyanide hydrogen cyanide phenol pka <= 10.0 pka = 3.46 a. The equilibrium favors the [Select] b. This reaction is best described as a(n) [Select] c. The strongest acid in the reaction is the [Select] [Select] d. The nucleophile in the forward reaction is e. The electrophile in the reverse reaction is [Select] phenolate %. ✓ reaction. 15 <
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Instructions: Answer the following questions regarding the test for carboxylic acids.
Answer questions a-c about the Bronsted acid-base reaction below using the identifying letters A-D below each structure. A table of pK, values for various organic and inorganic acids can be found in the references section. CH₂ -NH3 A ethylammonium + CH₂ B ethoxide CH₂ "NH₂ + CH₂ C ethylamine a) The weaker base is b) Its conjugate acid is c) The species that predominate at equilibrium are (two letters, e.g. AC) OH D ethanol
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