JUllent in rhubarb found to have anti-tumor properties. Rhein, the third PLUSIS, and prevention of metastasis. Aloe-emodin is 1, was capable of inhibiting cellula anthraquinone, is less well studied. This compound could effectively inhibi e in tumor cells, caused changes in membrane-associated functions and le e synthesis today is an example of an intramolecular Friedel Crafts react hat you have learned use a Lewis acid, this reaction does not. You shou what takes the place of the Lewis acid and the mechanism for the react oto -ОН H₂SO4 A ment e reaction in your lab book and record the relevant physical dat 5 well as the product rated ead the

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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Draw the mechanism for the following reaction. Draw the resonance structures for a generic acylium ion. Indicate which is the primary one and explain why.
Tather differen
Omponent in rhubarb found to have anti-tumor properties. Rhein, the third m
apoptosis, and prevention of metastasis. Aloe-emodin is an
, hodin, was capable of inhibiting cellular
anthraquinone, is less well studied. This compound could effectively inhibit t
e in tumor cells, caused changes in membrane-associated functions and led
e synthesis today is an example of an intramolecular Friedel Crafts reaction
hat you have learned use a Lewis acid, this reaction does not. You should
what takes the place of the Lewis acid and the mechanism for the reaction
H₂SO4
g=c
A
-ОН
ment
e reaction in your lab book and record the relevant physical data
as well as the product generated. Read the Material Safety Data S
Transcribed Image Text:Tather differen Omponent in rhubarb found to have anti-tumor properties. Rhein, the third m apoptosis, and prevention of metastasis. Aloe-emodin is an , hodin, was capable of inhibiting cellular anthraquinone, is less well studied. This compound could effectively inhibit t e in tumor cells, caused changes in membrane-associated functions and led e synthesis today is an example of an intramolecular Friedel Crafts reaction hat you have learned use a Lewis acid, this reaction does not. You should what takes the place of the Lewis acid and the mechanism for the reaction H₂SO4 g=c A -ОН ment e reaction in your lab book and record the relevant physical data as well as the product generated. Read the Material Safety Data S
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