Draw the product formed when (CH3CH₂CH₂CH₂)₂CuLi is treated with 17.38 each compound. In some cases, no reaction occurs. a. b. & d. OCH₂ then H₂O then H₂O
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- 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 400Draw the product formed when each compound is treated with two equivalents of CH;CH,CH,CHgMgBr followed by H,0. OCH3 a. b. C. CH;CH2 OCH2CH3What is the reagent needed for the following reaction? Ob ) b e O a 0 c Od N a. HCI b. LiAlHa c. DIBAL d. H₂, Raney Ni e. NaCN
- Which product is formed by the reaction of the compound shown with NaBH4? A. B. OH OH 1. NaBH4 2. H3O+ C. D. OH OHDraw the product formed when A is treated with each series of reagents.a. [1] H2O; [2] NaH; [3] CH3Brb. [1] CuCN; [2] DIBAL-H; [3] H2O c. [1] C6H5NH2; [2] CH3COClCI 107. Draw the curved arrow mechanism, including all intermediates, for the following reaction. 1 equiv. HCI 45 °C
- 6. Draw the products formed from nitration of each compound OH OH a. b. CH3 ČHaDraw 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 product formed when phenylacetic acid (C6H5CH2COOH) is treated with each reagent. With some reagents, no reaction occurs. a. NaHCO3 b. NaOH c. SOCl2 d. NaCl e. NH3(1equiv) f. NH3, ∆ g. CH3OH, H2SO4 h. CH3OH, −OH i. [1] NaOH; [2] CH3COCl j. CH3NH2, DCC k. [1] SOCl2; [2] CH3CH2CH2NH2 (excess) l. [1] SOCl2; [2] (CH3)2; [2] (CH
- Draw a stepwise mechanism for each reaction. NHNH2 a. NH,NH2 pyridine H Cr H2O b. -OH НО4. Complete the following reaction. reagent X H. HCN a) A в reagent Y b) OHDraw the product formed when pentanal (CH;CH,CH2CH;CHO) is treated with each reagent. With some reagents, no reaction occurs. a. NaBH4, CH,OH b. [1] LIAIH4; (2] H20 c. H2, Pd-C d. PCC e. NazCr,07, H2SO4, H2O f. Ag,0, NH,OH g. [1) CH,MgBr; (2] H2O h. [1] CęH,Li; [2] H20 i. [1] (CH3),CuLi; (2] H2O j. [1] HC=CNa; [2] H2O k. [1] CH;C=CLi; [2] H2O I. The product in (a), then TBDMS-CI, imidazole