13.42 Predict the products of the following reactions. A 2 OMe (a) (1) A (2) NaBH...
2. Draw products of following reactions. OMe 0 CH3NH2 (aq) Me CH3NH2 (aq) oMe OME CH3CH2NH2 (aq) Meo (iv) OME CH3CH2NH2 (aq) CH3 H₃ C CH NH₂ Ome
Predict the products of the following reactions но он ,н. 1. NaBH, 2. Hot
Pericyclic Reactions 1. Predict the products of the following reactions and propose a mechanism that explains it Me a heat OMCN heat 9. Ome =-COME HOY Y hest MeOC 2. Propose a synthesis of the following molecules using acetaldehyde as your only starting material 3. Propose a mechanism for the following transformations Meo,
pls help Clearly indicate stereoisomers, unless otherwise indicated. 1. Predict the products of the following reactions. a. H O DCC HCI I HOPh H2O c. ☺ NaOH 1) SOCl2, A 2) AICI: VHO 2. Suggest starting materials for the following reactions. b. acetone i) LiAIH4 Meo ii) H20 workup
2. Draw products of following reactions. CH3NH2 (aq) Meo CH3NH2 (aq) Ome CH3CH2NH2 (aq) Meo (iv) OME CH3CH2NH2 (aq) CH3 OMe H3C-NH2
Please name the products of each reaction 39. Predict the products of the following reactions a. butan-2-one & diethylamine NaBH(0Ac)} - - - NaBH(04)3, b. 4-fluropyradine Na OCH₂CH3 оснасHз O Na OCHz Ctyy Na OCH₂ CH3) Sandinerer reaction. c. 3 nitroaniline 1.HCl, Nano NH2 2. Cubr d. butan-2-one 1. KCN, HCN. 2.LAH EINO2 CH-NH2 NO2 NU e. cyclopentanone lanoline, tt. 2.LA 1. (CH3)3 N f. 2- bromopontane hoffman elimination NH. 2. Ag2O, A NH2 ZI LAH NHCHE, Nret Huntet EtzNH...
1. Predict the major organic products of the following reactions. Draw all stereoisomers that are formed. НО, OH 1 eq ,H2SO4 (assume H2O workup of reaction to neutralize product) 1. LDA 2. (assume H,O workup of reaction to neutralize product) 3. Hg(OAC)2 4. NaBH, EtOH 1eq HBr EtOH ambiente 1. Brz. CCL 2. NaOET, ETOH OH
predict the products and indicate the relative stereochemistry for the following transformations. When necessary indicate the major product. Me 1. light 2. xylenes, heat Et (d) (4 points) CN xylenes, heat Me 2. H30+, heat 3. Me OH Me Me cat p-TsOH, PhH reflux (d) (4 points) Meo OMe 1. AczO, pyridine Meo 2. HO HO OH Me 1. light 2. xylenes, heat Et (d) (4 points) CN xylenes, heat Me 2. H30+, heat 3. Me OH Me Me cat...
Predict the products Predict the Product. Provide the stable organic product(s) for each reaction below NaBH CHOH 1 2 HCI, H,0 NaBH, (1 вg.)., сн,он 1. 2. HC, н,о 1. NaBH(осH (1 eq.), сн,он CI 2. HCI, H,O 1. LIAIH (1 eq.), THF Br 2. HCI, H2O
IVA. Predict the organic products formed in each of the following reactions of acetophenone. (12 points) .H,O 1. PhMgBr, Et, 2. H2O 1. NaBH, CH,OH 2. H,O* 2 CH,CH,OH, H,00 IVB. Show a detailed mechanism (using curved arrows) for the Grignard reaction in question IVA between acetophenone and phenyl magnesium bromide (6 points)