Label the α and ẞ carbons in each alkyl halide. Draw all possible elimination products formed when each alkyl halide is treated with K-OC(CH3), b. ان Br

Draw the structure(s) for the major final product(s) formed in the following reaction sequence. CN ༼་་ SO 503 H₂SO4 Cl FeCl3 Click and drag to start drawing a structure.

Draw the products formed when phenol(C6H5OH) is treated with each reagent. Give an explanation. d. (CH3CH2)2CHCOCl, AlCl3 j. product in (d), then NH2NH2, – OH

Draw out each compound to clearly show what groups are bonded to the carbonyl carbon. Label each compound as a ketone or aldehyde. a. CH 3CH 2CHO b. CH 3CH 2COCH 3 c. (CH 3) 3CCOCH 3 d. (CH 3CH 2) 2CHCHO

Draw the organic products formed when cyclopentene is treated with each reagent. With some reagents, no reaction occurs. a.H2 + Pd-C b.H2 + Lindlar catalyst c.Na, NH3 d.CH3CO3H e.[1] CH3CO3H; [2] H2O, HO− f.[1]OsO4 + NMO; [2] NaHSO3, H2O g.KMnO4, H2O, HO− h.[1] LiAlH4; [2] H2O i. [1] O3; [2] CH3SCH3 j.(CH3)3COOH, Ti[OCH(CH3)2]4, (−)-DET k.mCPBA l.Product in (k); then [1] LiAlH4; [2] H2O

Draw the organic product(s) formed when CH3CH₂CH₂OH is treated with each reagent. a. H₂SO4 d. HBr g. TsCl, pyridine b. NaH h. [1] NaH; [2] CH₂CH₂Br e. SOCI₂, pyridine f. PBr3 c. HCI + ZnCl₂ Hint: NaH deprotonates the alcohol forming an alkoxide

Nitesh

Draw the organic product(s) formed when CH3CH2CH2OH is treated with each reagent. a.H2SO4 b.NaH c.HCl + ZnCl2 d.HBr e.SOCl2, pyridine f.PBr3 g.TsCl, pyridine h. [1] NaH; [2] CH3CH2Br [1] i.TsCl, pyridine; [2] NaSH j.POCl3, pyridine

Complete the reactions given below

Show reagents and experimental conditions you might use to convert propyne into each product. (Some of these syntheses can be done in one step; others require two or more steps.)