When propenal is treated with sodium acetylide, a product is formed whose IR spectrum exhibits a broad absorption between 3200 and 3600 cm¯1, but shows no absorption near 1700 cm-1. (a) Draw the structure of the product. (b) Argue whether the nucleophile adds reversibly or irreversibly to the carbonyl group. CH HC || CH2 1. HC=CNa ? 2. NH,CI
When propenal is treated with sodium acetylide, a product is formed whose IR spectrum exhibits a broad absorption between 3200 and 3600 cm¯1, but shows no absorption near 1700 cm-1. (a) Draw the structure of the product. (b) Argue whether the nucleophile adds reversibly or irreversibly to the carbonyl group. CH HC || CH2 1. HC=CNa ? 2. NH,CI
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:When propenal is treated with sodium acetylide, a
product is formed whose IR spectrum exhibits a broad
absorption between 3200 and 3600 cm¯1, but shows
no absorption near 1700 cm-1. (a) Draw the structure
of the product. (b) Argue whether the nucleophile adds
reversibly or irreversibly to the carbonyl group.
CH
HC
||
CH2
1. HC=CNa
?
2. NH,CI
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