11. 1) Consider the two halves of the naphthalene as separate-which is more reactive? 2) Which position in the more reactive ring is most reactive? (There is only one major pdt.) OMe ळ con HNO3 12. Assume the kinetic product for sulfonylation unless otherwise indicated. O₂N H2SO4 (fuming)

11. 1) Consider the two halves of the naphthalene as separate-which is more reactive? 2) Which position in the more reactive ring is most reactive? (There is only one major pdt.) OMe ळ con HNO3 12. Assume the kinetic product for sulfonylation unless otherwise indicated. O₂N H2SO4 (fuming)

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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Question

11. 1) Consider the two halves of the naphthalene as separate-which is more reactive?
2) Which position in the more reactive ring is most reactive? (There is only one major pdt.)
OMe
ळ
con HNO3
12. Assume the kinetic product for sulfonylation unless otherwise indicated.
O₂N
H2SO4
(fuming)

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