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help with all of them please 1) Complete the following reactions OH H2SO4 (a) (b) OH...
1) Complete the following reactions OH OH H2SO (b) (c) H2SO4 H,SO heat heat heat OH OH H.CO H.COM H.CO. OH f) 2) Show how to convert (a) 1-Propanol to 2-propanol in two steps (b) Cyclohexene to cyclohexanone in two steps (c) Propene to propanone (acetone) in two steps. 3) Write a stepwise mechanism for the sulfonation of benzene. Use HSO3 + as the electrophile.
9) Identify the electrophile in the sulfonation reaction of benzene. 2 Pt A. SO2 B. H2SO4 C. Sos* D. H2SO3 E. SO3 10) Write the mechanism for the following EAS reaction? 4 Pt CI. AICI 11) Predict the all possible products for the following reactions and circle the major product among them? 8 Pt olub HNO3. H,SO A) Yo Cl2, AICI: B) CH,CI, AICI: Сн, HNO3, H2SO4 D) OH
complete the following reactions with the proper stereochemistry as need оCHbb H2SO4 (dilute) OH H2O HBr (conc) но H но heat но но H CHs MCPBA OH Jones (CrO3. H,SO4) H2O, acetone 1. MCPBA OH PCC 2. NaCN 3. Hy0 pyridinium chlorochromate CH2CI2, 25 C 1. MCPBA PCC OH pyridinium chlorochromate 2. HBr Cн-Cl, 25 C NaBH OH Hао 1. DMSO, (COCI)2, -60C 1. LIAIH 2. Et N 2. H,0 оCHbb H2SO4 (dilute) OH H2O HBr (conc) но H но...
1.Predict all the products for the following reaction. Which is the major product? Why? + conc. H2SO4 heat OH 2. Give an alcohol that you could use to synthesis each of the following alkenes? din 3.Draw the mechanisms for the following two schemes (two separate mechanisms). Only show the mechanism for the most stable product for each scheme. What is the key difference in the mechanistic steps between these two reactions? ОН ОН conc H2SO4 conc H2SO4 heat heat
please help in all sections asap!! Which of the following reactions would produce isopropylbenzene as the major product? ОН AICI: H2SO4 H2SO4 AICI3 IV I all of these Predict the product for the following reaction fuming H2SO4 SO3H Predict the structure of the major product for the following reaction Which of the following compounds will not undergo nucleophilic aromatic substitution? 1-chloro-2,4-dinitrobenzene 1-bromo-4-nitrobenzene O-chloronitrobenzene m-chloronitrobenzene p-chloronitrobenzene Choose the correct sequence of reagents for the following transformation. 2) 3 . NH2 2)...
8.34 Draw a mechanism for each of the following E1 processes: OH Br conc. H2SO4 Heat БЕТОН Heat (b) EtOH. Her (C) ОН conc. H2SO4 Heat OPUS (d) D
Application Questions 1. Predict all the products for the following reaction. Which is the major product? Why? conc. H2SO4 heat OH 2. Give an alcohol that you could use to synthesis each of the following alkenes? o in s 3. Draw the mechanisms for the following two schemes (two separate mechanisms). Only show the mechanism for the most stable product for each scheme. What is the key difference in the mechanistic steps between these two reactions? ОН conc H2SO4 heat...
4. Complete the mechanism for the following reactions. (8pt) HgSO4 H2O, H2So4 а. 1. Sia2BH b. 2. H202, NaOH No need to show the C-B to C-OH step. ons. M
following reactions. If reagents are added in separate steps, don't forget to number them. NH2 OH он NH b) 1) NaOCH2CHs H2CHs 2) neutralize (add second) c) 1. NaCN 2. LiAIH4 3. H20 d) NaOH OH он HN 1) excess CH3CH2MgBr 2) neutralize
please help in all sections!! Provide the reagents necessary to carry out the following conversion. OH -OH 1. LAIH/H20 2 KCN/HCN 1 KCN/HCN 2. H₂O 1. NaBH/CH OH 2. H₂O Provide the product for the following reaction Но* Br HOCH2CH2OH Mg/ether H2SO4 2. H,0 но оно о оо ОН Provide the reagents necessary for the following conversion Br O 1. NaBH/CH3OH 2. CH3CH2MgBr CH3CH2 Mg Br/ether 1. H30 2. CH3CH2MgBr/ether 1. CHCH2Mg Br/ether, 2. H₂OT, A Rank the following compounds...