Example 1H. The aldol reaction between A and B produces the a-ß unsaturated (tri- substituted) product C. A + BC C₂H₂O CzH14O Given that the para-substituted substrate A can be synthesize from Friedel Craft's acylation; and the IR and HNMR spectrum of B provided below, deduce the structure of A, B and C
Example 1H. The aldol reaction between A and B produces the a-ß unsaturated (tri- substituted) product C. A + BC C₂H₂O CzH14O Given that the para-substituted substrate A can be synthesize from Friedel Craft's acylation; and the IR and HNMR spectrum of B provided below, deduce the structure of A, B and C
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:Example 1H. The aldol reaction between A and B produces the a-ß unsaturated (tri-
substituted) product C.
C12H14O
Given that the para-substituted substrate A can be synthesize from Friedel Craft's acylation;
and the IR and ¹HNMR spectrum of B provided below, deduce the structure of A, B and C
IR spectrum of B
Percent Transmission (Transmitance)
3
0.8
0.6
0.4
0.2
¹H NMR spectrum of B
A + B
CgH8O
3000
INFRARED SPECTRUM
2000
Wavenumber (cm-1)
PPM
1000
Provide reasons for your deduction. *Hint: fragment of m/z = 132 observed in abundance for
product C.
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