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- 6. Given the reactions below, provide the missing products and explain the differences among the hydride reactions. Where is stereochemistry is present, does it change or stay the same? 1. LİAIH4, THF 1. NaBH4, EtOH 2. H;O* 2. H3O* + NH 1. LİAIH4, THF 1. NABH4, EtOH 2. H3O* 2. H;O* ОН 1. LİAIH4, THF 1. NaBH4, ETOH 2. H3O* 2. H3O*What is(are) the major product(s) of the following reaction? 1. ВНз, THF . ............. 2. NaOH, H202 OH HO OH OH II HO II IV Select one: O II, II O II, IV O II, V O IV, VReagents a. C6H5CHO b. NaOH, ethanol h. BrCH2CH=CH2 i. Na* OEt, ethanol j. Br2, H* k. K* t-BuO c. Pyrrolidine, cat. H* d. H2C=CHCN e. H3O* f. I. CH2(CO2ET)2 -CH2CH2CN LDA m. heat g. ELOC(=0)CO2ET Select reagents from the table to synthesize this compound from cyclopentanone. Enter the letters of the chosen reagents, in the order that you wish to use them, without spaces or punctuation (i.e. geda).
- 1. For the reaction (CH3)2O + C₂H5F → [(CH3)2OC₂H5]+F¯ (a) draw the structure for the cationProvide the organic product(s) of the following reaction. .CI 1. Mg, ether 2. CO2 3. HСІ, Н208. a) b) Provide structure(s) for the starting material(s), reagent(s) or the major organic product(s) of each of the following reactions. OEt COOH CH3 CH; 0 OH 1. LiAlH4, ether 2. HO OH ند (CH3COO NaOH, H₂O 5 CH 3 Cl
- predict the major organic products if of the 'following reactions a. ОН 1. TSCI, Py 2. МеОН, Д b. NaOEt Br С. CI acetonitrile KCN d. Br DBU Br.. e. OH NaOMe HOME f. H2N HO,Question 20 (Mandatory) (5 points) Which of the following has(have) a higher oxidation state of carbon than the carbon in formaldehyde, H₂C=O? 1. CH3OH II. HCO₂H III. H₂CO3 ||| II and III I. II. and IIIWhat is the product of the following reaction? 1. B2Н6. THF 2. NaOH, H2O2 он HO С. А. В. D.
- 4. Which is the major product of this reaction? а. b. C. OH d. 1. FeCl3, CI 2. Hа/Pd16. Predict the products of the following reactions. ( a. Br 1. Mg/ether 2. CO2 3. H,O* b. NH d. HO Br CN 1. LDA e. 2. CH;CH,IQUESTION 4b Draw the structures of the major organic compound products A - H (in he boxes) for the scheme shown below. B H Sn/HCI NaOH C HNO/H₂SOA conc. SO / H₂SO Na2Cr2O7. H2SO4/H2O H₂NNH2, KOH E AICI, G to OH NBS. ROOR, A LL F conc. = concentrate