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Please answer all of them in detail 14. Provide all of the organic products for the following transformations: A. i Bra, CHCI B 1. Hg(OAC)2, H2O 2.NaBHA OH C. SOCI2 CH3 Me D. 1. BH3 2. NaOH, H2O2
14. Provide all of the organic products for the following transformations: A. Å Br2, CH2CL2 B. 1. Hg(OAC)2, H2O 2.NaBH4 OH C. SOCI2 CH3 Me D 1. BH3 2. NaOH, H2O2
1 2 3 $ 4 % 5 & 7 ob Q W E R T Y page 11 8 9. Show all possible products (major and minor) for the reactions below. Specify if the reaction is stereospecific. NaOH CH₃ ? Br CH3-CH2-ONa Ph.. Br Base (KOH) OH CHE! H30*
2 # 3 $ 4 % 5 6 tab Q W Y page 14 B 8 12. Complete the following reaction. Draw the complete, detailed mechanism for the following reaction. Assume that it takes place via SN mechanism. Will the reaction produce a single stereoisomer, or will it produce a mixture of stereoisomers? If it produces a mixture, then will the isomers be produced in equal amounts? Br. ? + HS
Please peovide a mechanism of the 3 16. What is the major organic product obtained from the following reaction? CH3 CHS CH HC OH но он он 1. ВН 2. H202. NaOH a. 1 b. 2 c. 3 d. 4 ANSWER: b 18. What is the major organic product obtained from the following reaction? 1. Hg(OAc) H20 2. NaBH он a. 1 b. 2 с. 3 d. 4 ANSWER: b 23. What is the major organic product obtained from the...
for f - j draw structures pls help with #1 as well f) 4-methyl-2-pentene 9) trans-8-ethyl-3-undecen h) E-5-bromo-4-chloro-7,7-dimethyl-4-undecene i) Z-1,2-difluoro-cyclohexene i) 4-ethenylcyclohexano Predict the major organic product or products of each of the following reactions. a) (CH3),CHCH-CH: H2SO4 HO b) (CH3),CHCH-CH, 1. Hg(OAc), H20 2. NaBH4 1. BH-THF c) (CH3),CHCH-CH2 2. H,O, NaOH
es 20 1 2 $ 3 % 5 tab Q W page 10 5 8. Using acetylene as one of the starting materials, show the synthesis of the following compound
Predict the products. 16. K2Cr207 (excess) H2SO4, H2O HO 1. Phli, Et20 2. HCI, H20 3. SOCI2, Etz 4. NaOAC 1. Mg (1 eq), Et O Br 2. (1 eq) | C-CHO 3. HCI, H20 1. NaBH, MeOH, 0°C 2. PBrz. THE 3. LiAIDA, THE 4. HCI, H20 1. SOCI, NEtz, THE CHO 2. 2 eq Li, hexane 3. HCI, H20 hint: multiple steps 1. LiAlH4, THE 2. HCI, H2O 3. PBr3, THE 1. PCC, DCM OH 2. Mg, Eto...
CHEM 241 Assignment 6 2. Provide the structure of the major products A, B, and C formed in each of the synthesis routes below. OH EINH Croz, H2SO A Hicat. B H, (-H20) 2) H30* В B ~ Br. 1 с LE A H30C b) H O V 2EOH cat (H20) 1) Hg(OAC). THE 2) NBH OAC - OCCH c) 1) POCI Me DMF - 2) NaHCO, (aq) Ph, P=CHCOMe - A Pdic. H C No Mg в с но...
Propose an efficient synthesis for the transformation below, using two sequential reductive aminations. Enter the appropriate number or letter from the reagent list handout. Propose an efficient synthesis for the transformation below, using two sequential reductive aminations. Enter the appropriate number or letter from the reagent list handout. Step 1 + NaBH3CN, H+, Step 2 - NaBH3CN, H+ Reagent List (Updated 4/30/2020) Enter # or letter in the appropriate boxes. Note: Exam responses are case insensitive Alkyl Halides (X = Cl,...