Draw the organic products formed when 2-bromopentan-3-one (CH3CH2COCHBrCH3) is treated with each reagent: (a) Li2CO3, LiBr, DMF; (b) CH3CH2NH2; (c) CH3SH
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Draw the organic products formed when 2-bromopentan-3-one (CH3CH2COCHBrCH3) is treated with each reagent: (a) Li2CO3, LiBr, DMF; (b) CH3CH2NH2; (c) CH3SH
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- Draw the organic products formed when cyclopentene is treated withfollowing reagent. (CH3)3COOH, Ti[OCH(CH3)2]4, (−)-DETDraw the products formed when phenol(C6H5OH) is treated with each reagent. Give an explanation. d. (CH3CH2)2CHCOCl, AlCl3 j. product in (d), then NH2NH2, – OHDraw the products formed when phenol(C6H5OH) is treated with each reagent. Give an explanation. c. CH3CH2Cl, AlCl3 l. product in (c), then KMnO4
- Draw the organic products formed when cyclopentene is treated withfollowing reagent. Na, NH3Draw the products formed when (CH3)2C=CH2 is treated with following reagent. [1] BH3; [2] H2O2, HO−Eleostearic acid, C18H30O2, is a rare fatty acid found in the tung oil used for finishing furniture. On ozonolysis followed by treatment with zinc, eleostearic acid furnishes one part pentanal, two parts glyoxal (OHC-CHO), and one part 9-oxononanoic acid [OHC(CH2)7CO2H]. What is the structure of eleostearic acid?
- Comparing Two Different Methods of Hydration of an Alkene Draw the product formed when CH3CH2CH2CH2CH=CH2 is treated with either (a) H2O, H2SO4; or (b) BH3 followed by H2O2, HO−.What product is formed when D-Gulose is treated with a. CH3I, Ag2O b. The product in (a), then H3O+ c. The product in (b), then C6H5CH2Cl, Ag2ODraw the products formed when p-methylaniline (p-CH3C6H4NH2) istreated with following reagent. CH3CHO, NaBH3CN