Compound A has the molecular formula C14H25Br and was obtained by the reaction of sodium acetylide with 1,12-dibromododecane. On treatment of compound A with sodium amide, compound B (C14H24) was obtained. Ozonolysis of compound B gave the diacid HO2C(CH2)12CO2H. Catalytic hydrogenation of compound B over Lindlar palladium gave compound C (C14H26), and hydrogenation over platinum gave compound D (C14H28). Further, C yielded O=CH(CH2)12CH=O on ozonolysis. Assign structures to compounds A through D so as to be consistent with the observed transformations.
Compound A has the molecular formula C14H25Br and was obtained by the reaction of sodium acetylide with 1,12-dibromododecane. On treatment of compound A with sodium amide, compound B (C14H24) was obtained. Ozonolysis of compound B gave the diacid HO2C(CH2)12CO2H. Catalytic hydrogenation of compound B over Lindlar palladium gave compound C (C14H26), and hydrogenation over platinum gave compound D (C14H28). Further, C yielded O=CH(CH2)12CH=O on ozonolysis. Assign structures to compounds A through D so as to be consistent with the observed transformations.
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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Compound A has the molecular formula C14H25Br and was obtained by the
reaction of sodium acetylide with 1,12-dibromododecane. On treatment of
compound A with sodium amide, compound B (C14H24) was obtained. Ozonolysis
of compound B gave the diacid HO2C(CH2)12CO2H. Catalytic hydrogenation of
compound B over Lindlar palladium gave compound C (C14H26), and
hydrogenation over platinum gave compound D (C14H28). Further, C yielded
O=CH(CH2)12CH=O on ozonolysis. Assign structures to compounds A through D
so as to be consistent with the observed transformations.
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