Under the conditions of this extractive procedure, how does aspirin become partitioned into the aqueous layer? How do we then recover this substance in a pure form from the aqueous layer? The acidic hydrogen in the carboxyl group (-COOH) of aspirin undergoes an acid-base reaction O1) with NaOH to form the conjugate base, sodium 2-acetoxybenzoate. U 2) This ionic species then readily dissolves in water. 3) Conversely, the organic unknown does not possess an acidic residue, so no acid/base reaction can осcur. 4) It therefore does dissolye in water.
Under the conditions of this extractive procedure, how does aspirin become partitioned into the aqueous layer? How do we then recover this substance in a pure form from the aqueous layer? The acidic hydrogen in the carboxyl group (-COOH) of aspirin undergoes an acid-base reaction O1) with NaOH to form the conjugate base, sodium 2-acetoxybenzoate. U 2) This ionic species then readily dissolves in water. 3) Conversely, the organic unknown does not possess an acidic residue, so no acid/base reaction can осcur. 4) It therefore does dissolye in water.
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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Transcribed Image Text:Under the conditions of this extractive procedure, how does aspirin become partitioned into the aqueous layer? How
do we then recover this substance in a pure form from the aqueous layer?
O 1) The acidic hydrogen in the carboxyl group (-COOH) of aspirin undergoes an acid-base reaction
with NaOH to form the conjugate base, sodium 2-acetoxybenzoate.
U 2) This ionic species then readily dissolves in water.
3) Conversely, the organic unknown does not possess an acidic residue, so no acid/base reaction can
occur.
4) It therefore does dissolve in water.
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