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Q: Draw the structure of (S,S)-ethambutol, a drug used to treat tuberculosisthat is 10 times more…
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Q: Draw the structure of (S,S)-ethambutol, a drug used to treat tuberculosis that is 10 times more…
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Q: Draw the structure of (S,S)-ethambutol, a drug used to treat tuberculosis that is 10 times more…
A: Detail drawing procedure of (S,S)-ethambutol in zigzag manner is given below
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Q: Draw the structure of (S,S)-ethambutol, a drug used to treat tuberculosis that is 10 times more…
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Q: Draw the structure of (S,S)-ethambutol, a drug used to treat tuberculosis that is 10 times more…
A: The stereo centres in the above molecule are as shown below
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A: Designate the compound R or S configuration.
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- Draw the structure of (S,S)-ethambutol, a drug used to treat tuberculosisthat is 10 times more potent than any of its other stereoisomers. (See attached)Determine the missing product X. 2 HC2H3O2 + K2CO3 --> H2O + 2 KC2H3O2 + X A. X= CO3 2- B. X= H2CO3 C. X= CO2 D. X= K2CO3 E. none of the above.How many stereogenic centers are present in the following tetraalkylammonium salt? Draw all possible stereoisomers.
- Electrostatic potential maps of anisole and thioanisole are shown. Which do you think is the stronger acid, p-methoxybenzoic acid or p-(methylthio)benzoic acid? Explain.The double bond of an enamine (alkene + amine) is much more nucleophilic than a typical alkene double bond. Assuming that the nitrogen atom in an enamine is sp2hybridized, draw an orbital picture of an enamine, and explain why the double bond is electron-rich.Thioglycolic acid, HSCH2CO2H, a substance used in depilatory agents (hair removers) has pKa = 3.42. What is the percent dissociation of thioglycolic acid in a buffer solution at pH = 3.0?
- A key step in the synthesis of the narcotic analgesic meperidine (tradename Demerol) is the conversion of phenylacetonitrile to X. (a) What isthe structure of X? (b) What reactions convert X to meperidine ?An acid–base reaction of (R)-sec-butylamine with a racemic mixture of 2-phenylpropanoic acid forms two products having different melting pointsand somewhat different solubilities. Draw the structure of these twoproducts. Assign R and S to any stereogenic centers in the products.How are the two products related? Choose from enantiomers,diastereomers, constitutional isomers, or not isomers of each other.Draw the products formed when p-methylaniline (p-CH3C6H4NH2) is treated with each reagent.a. HClb. CH3COClc. (CH3CO)2Od. excess CH3Ie. (CH3)2C = Of. CH3COCl, AlCl3g. CH3CO2Hh. NaNO2, HCli. Part (b), then CH3COCl, AlCl3j. CH3CHO, NaBH3CN
- a. Draw a three-dimensional structure for the following steroid. b. What is the structure of the single stereoisomer formed by reduction of this ketone wrth H2, Pd-C? Explain why only one stereoisomer is formed.An acid–base reaction of (R)-sec-butylamine with a racemic mixture of 2phenylpropanoic acid forms two products having different melting points and somewhat different solubilities. Draw the structure of these two products. Assign R and S to any stereogenic centers in the products. How are the two products related? Choose from enantiomers, diastereomers, constitutional isomers, or not isomers of each other.Rank the labeled N atoms in the anticancer drug imatinib (trade name Gleevec) in order of increasing basicity. Imatinib, sold as a salt with methanesulfonic acid (CH3SO3H), is used for the treatment of chronic myeloid leukemia as well as certain gastrointestinal tumors.