ОН 1. PBr3; 2. Na Ng HNO3 H₂SO4 ke- -CH3 CH3C) AICI NO2 он Socl2 4....
products for the Provide the major reactions. Include stereochemistry where relevant where no reaction occurs, following write NR. -ci AlCl3 .NO2 Hz (9) Pdlc -CH3 SO3 H₂SO4
4. Reactions Provide the major products for the following reactions. Include Stereochemistry where relevant where no reaction, occurs, write NR. Bra FeBrz 0 CH3 CI OH AIC3 NEC Fell H2O H₂SO4
4 Reactions Provide the major products for the following reactions. Include stereochemistry where relevant where no reaction occurs, write NR. .....н НВК Оң
4. Reactions Provide the major products for the reactions. Include stereochemistry where relevant where no reaction occurs, following write NR. Brz 1. CH₃ Li 2. HLI
1 9. Arrange the following in ng compounds in increasing (weakest to strongest) order of basicity. NH2 NH2 NO2 E. None of the above What is the product of the following sequence? 10. H3C CH3 OH он Na V. A I What is the major product for the following Reaction? 11. Pd(OAc)h PPhy Et N NO2 NO2 NO2 C.Ⅲ A. I D. IV V. 12. Predict the product for the following reaction. Br 1. NaNs 2. LiAIH4 3. H20 1...
Dr. Good chem observed the Reactions shown in figure I Product 2 1. H₂SO4/HNO3 2.0l2/AC3 1. CI2 AICI: Pnduct 2. H₂ Sby / HNO₃ 1 To his surprise Dr. Goodchem received 2 different products from this reaction. Please explain to Dr. Good chem what happened.
CH3 . . H I CoHs + KOH CH3CH2OH Сң,Сн, хүн heat Br CHCCH,CHE + dilute Na*CN + CH3CH2OH CH3 он- ..C-Br Agt Ha но For each of the following reactions, predict the major product(s), showing proper stereochemistry where appropriate. Write N.R. if no reaction occurs. Identify the type of substrate (1º, 2º, 3º, allylic, benzylic, aryl, vinyl) and give the type of mechanism by which each product is formed (Sni, Sy2, E, E). Assume the reaction is at room...
7.2 b) c) Draw the major organic product(s) of the following reaction. CH3 H3C-C-CEC-H | NaNH, / NH (1) more pollastre CH3CH2–1 CH3 • You do not have to consider stereochemistry. • If no reaction occurs, draw the organic starting material. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. • Separate multiple products using the + sign from the drop-down menu. Draw the organic product(s) of the following reaction. NaOC2H5...
(2) NaBH4 (2) H202 OH cold, dilute KMnO4 "ОН H,C H,C HCO,H H,O с-с CH CH2CH, CH,CH2CH Predict the major products of the following reactions, including stereochemistry where appropriate. (a) (R)-2-butanol + TsCl in pyridine c) cyclooctanol + CrO3/H2SO4 (e) cyclopentylmethanol + Na2Cr 01/H2SO4 (g) n-butanol + HBr (i) potassium t-butoxide + methyl iodide (k) cyclopentanol + H2SO4/heat (m) sodium ethoxide +1-bromobutane (b) (S)-2-butyl tosylate +NaBr (d) cyclopentylmethanol + CrOs pyridine HC cyclopentanol + HCI/ZnCl2 (h) cyclooctylmethanol + CH3CH2MgBr (G)...
1) Predict the Products: Using line drawings with proper use of dashed wedge and solid wedge notation where necessary, draw the major organic products of the following reactions in the boxes provided. If no reaction occurs write “no reaction” or “N.R.” in the box. Include stereochemistry in your answers where appropriate. If a product is racemic draw both enantiomers or write “racemic” next to the structure. Assume all reagents written above and below the arrows are present in excess unless...