Q: CH3CH2CH2CH2CHO) is treated with each reagent.
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Solved in 4 steps with 7 images
- I. What products are formed when each alcohol is oxidized with K2Cr207? a. CH;CH,CH2CH;CH2OH ОН ОН H3C CH3 b. C.Draw the products formed when each compound is treated with CH;CH,COCI, AICI3. CH(CH3)2 N(CH)2 Br CH3 CH(CH)2 a. b. C. d. е.Draw the products formed when phenol (C6H5OH) is treated with each set of reagents. a. [1] HNO3, H2SO4; [2] Sn, HCl b. [1] (CH3CH2)2CHCOCl, AlCl3; [2] Zn(Hg), HCl c. [1] CH3CH2Cl, AlCl3; [2] Br2, hν d. [1] (CH3)2CHCl, AlCl3; [2] KMnO4
- 3. What product is formed when HO(CH₂) CHO is treated with each reagent? c. Ag₂O, NH OH d. Na₂Cr₂O₂, H₂SO4, H₂O a. NaBH, CH₂OH b. PCC 400What alkenes are formed when each alcohol is dehydrated with TSOH? Label the major product when a mixture results. OH Xom OH a. OH b. CH₂CH3 OH C. d. CH₂CH₂CH₂CH₂OH e.Does the equilibrium favor the reactants or products in each substitution reaction? a. CH;CH2-NH2 Br CH;CH2-Br + "NH2 b. "CN CN + I-
- What alkenes are formed when each alcohol is dehydrated with TSOH? Label the major product when a mixture results. CH2CH3 OH он OH b. d. CH;CH2CH2CH2OH а. C. е. ОнDraw the products formed when each ether is treated with two equivalents of HBr. a. (CH3),COCH,CH,CH3 b. С. FOCH3Draw the products of each reaction, including stereochemistry. Br2 a. b.
- 1. Draw the products in each reaction. a. H b. CH3-C-CH₂CH3 CI -OH K+ -OC(CH3)3 CH₂CH3 a Xa C. d. CH₂CH₂OH CH3CH₂O™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 alkoxideDraw 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