19 How many hydrogen atoms are connected to the indicated carbon atom? Select the right answer from the Table. a CH3 b Answer Answer for a Answer for b Answer for c A 1 2 0 B 0 2 1 C 3 0 2 D E 2 1 1 3 1 2 28 Tamoxifen is an anti-breast cancer drug that is an antagonist of the estrogen receptor in breast tissue. How many carbon atoms Tamoxyfen has? A. 23 B.24 C.25 D26 right a answer E. 27 6

19 How many hydrogen atoms are connected to the indicated carbon atom? Select the right answer from the Table. a CH3 b Answer Answer for a Answer for b Answer for c A 1 2 0 B 0 2 1 C 3 0 2 D E 2 1 1 3 1 2 28 Tamoxifen is an anti-breast cancer drug that is an antagonist of the estrogen receptor in breast tissue. How many carbon atoms Tamoxyfen has? A. 23 B.24 C.25 D26 right a answer E. 27 6

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

Chapter22: Organic And Biological Molecules

Section: Chapter Questions

Problem 172CP: Estradiol is a female hormone with the following structure: How many chiral carbon atoms are in...

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1. Use the image provided to answer the question in detail: a) Two of the earliest drug molecules featured in Chapter 8 are Vicodin and Heroin, whose chemical structures are very similar. Both of these molecules contain an amine functional group and several rings. Indicate the number of aromatic rings in each structure, and identify the amine functional group in each molecule as primary, secondary, or tertiary.
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Estradiol is a female hormone with the following structure: How many chiral carbon atoms are in estradiol?
Estrogens are female sex hormones, the most potent of which is B-estradiol. OH AYA Но B-Estradiol In recent years, chemists have focused on designing and synthesizing molecules that bind to estrogen receptors. One target of this research has been nonsteroidal estrogen antagonists, compounds that interact with estrogen receptors and block the effects of both endogenous and exogenous estrogens. A feature common to one type of nonste- roidal estrogen antagonist is the presence of a 1,2-diphenylethylene with one of the benzene rings bearing a dialkylaminoethoxyl substituent. The first nonsteroidal estrogen antagonist of this type to achieve clinical importance was tamoxifen, now an important drug in the treatment of breast cancer. Tamoxifen has the Z configuration shown here. NMeg A B NMeg ? ОН Tamoxifen Propose reagents for the conversion of A to tamoxifen. Note: The final step in this synthesis gives a mixture of E and Z isomers.
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