Vhen the halohydrin is treated with NaH, a product of molecular formula C¸H§O is formed. Draw the ructure of the product and indicate its stereochemistry. он CH3 CH draw structure .
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Q: When attached halohydrin is treated with NaH, a product of molecular formula C4H8O is formed. Draw…
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- When attached halohydrin is treated with NaH, a product of molecular formula C4H8O is formed. Draw the structure of the product and indicateits stereochemistry.When each halohydrin is treated with NaH, a product of molecular formula C4H8O is formed. Draw the structure of the product and indicate its stereochemistry.Draw the products formed when cembrene A is treated with O3 followed by CH3SCH3. Label each product as chiral or achiral
- Draw the products formed (including stereoisomers) when attached compound is reduced with NaBH4 in CH3OH.Draw the products formed when attached alkene is treated with BH3 followed by H2O2, HO−. Include the stereochemistry at all stereogenic centersAn 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.
- Clopidogrel is the generic name for Plavix, a drug used to prevent the formation of blood clots in patients that have a history of heart attacks or strokes. A single enantiomer of clopidogrel can be prepared in three steps from the chiral αhydroxy acid A. Identify B and C in the following reaction sequence, and designate the conguration of the enantiomer formed by this route as R or S.Draw the products formed when p-methylaniline (p-CH3C6H4NH2) istreated with following reagent. Part (b), then CH3COCl, AlCl3Draw the products formed when CH3COCH2CH2CH = CH2 is treated with each reagent:(a) LiAlH4, then H2O;(b) NaBH4 in CH3OH;(c) H2 (1 equiv), Pd-C;(d) H2 (excess), Pd-C;(e) NaBH4 (excess) in CH3OH;(f) NaBD4 in CH3OH.
- Draw the products obtained (including stereochemistry) when each compound is treated with LDA, followed by CH3I.Draw the product formed when phenylacetic acid (C6H5CH2COOH) istreated with following reagent. With some reagents, no reaction occurs. CH3NH2, DCCName the structure and give it's stereogenic centers as well as it's stereochemistry (R or S)