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The acid-catalyzed reaction of 4,4-dimethylcyclohexa-2,5-dien-1-one resulted in the formation of a compound, the NMR data of which are given below. For N: 1HNMR(300MHz,CDCl3);=6.95(d,J=8.0Hz,1H),6.61(d,J=2.8H,ll),6.57 (dd,J=8.0,2.8Hz,1H),5.39 (bs,
The acid-catalyzed reaction of 4,4-dimethylcyclohexa-2,5-dien-1-one resulted in the formation of a compound, the NMR data of which are given below. For N: 1HNMR(300MHz,CDCl3);=6.95(d,J=8.0Hz,1H),6.61(d,J=2.8H,ll),6.57 (dd,J=8.0,2.8Hz,1H),5.39 (bs, 1H),2.16(s,3H),2.14(s,3H),13CNMK(109MH/,CDOl3); 153.4,137.9,130.4,128.6,116.6,112.3,19.8,18.7. 4.4. Find the structure of product N and propose a plausible mechanism
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Quantitative Chemical Analysis
Authors: Daniel C. Harris
9th Edition
146413538X, 978-1464135385
