C. Problem 16-71 How would you synthesize the following compounds from benzene? Assumethat the ortho and para isomers can be separated. You don't need to show mechanisms,only reagents.i)CH3AVC312 Brz Al Brz2 HNO3, H₂50402NBr C. Problem 16-71 How would you synthesize the following compounds from benzene? Assumethat the ortho and para isomers can be separated. You don't need to show mechanisms,only reagents.i)CH3AVC312 Brz Al Brz2 HNO3, H₂50402NBr

Both the synthesis methodologies are given in figureplease see it very carefully because any changes…

Answered: C. Problem 16-71 How would you…

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter16: Chemistry Of Benzene: Electrophilic Aromatic Substitution

Section16.10: Synthesis Of Polysubstituted Benzenes

Problem 22P

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Provide the following names of the following. Answer from left to right.
15-41 Compound A(C5Hh, is not optically active and cannot be separated into enantiomers. It reacts with bromine in carbon tetrachloride to discharge the purple color of bromine and form Compound B( C.FL Br,). When Compound A is treated with H., in the presence of a transition metal catalyst, it is converted to compound C(C5H10). When treated with HC1, compound A is converted to compound DtC.HyCl). Given this information, propose structural formulas for compounds A B, C, and D. Hint: There are at least three possibilities for Compound A and, in turn, three possibilities for Compounds B. C, and D.
Pls help on both 14,15
Synthesize the following compounds starting from benzene. Reactions contain more than two steps. Assume that you can separate ortho and para isomers if necessary
14-5:
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