Complete the following reactions: OH CH OH BgCrgOy, H2SO4 E Cr207 H,804 CH OH AICI (b)...
Complete the following reactions KMnO4 / heat NH2 AICI 2/CuCl OH HO 1. CH;CH2Cl/ AlCl 2. KMnO4 3. HNO3/ H2SO4 4. SnCl2/H3o AlCl Br2 /FeBr3 AlCl CI /AlCl 3. KMno
Complete the following scheme. Two step reactions will contain two boxes. MgBr H AICI: 2. H 3. PCC, CH.CZ O H 2. H 3. H.CO OH 1. OH 2. Final product shows strong absorbance at 1700 cm-1 H-NMR singlet located downstream - 13.5 ppm H H Final product shows a strong absorbance at 1 700 cm-1 H-NMR signal located downstream-9.72 ppm АІСІ,
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...
How do I do the following reactions?
OCHS CH,CHа AICI HNO3 CH3CH2CH,CI H2SO4 n. CO, HCI 2 NH3 AICI, CuCl heat, pressure q.O2N NO2 CH2CH3 CH2CH2CH Na2Cr2O7 Br2 H',heat light "CHз S.
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.
3. Draw the product for the following reactions H₂Cro4 H3O* & acetone (Jones' reagent) 1. OH H2Cro4 H3O+ acetone (Jones' reagent) 2. CH3-CH2-OH 3. OH PCC CH2Cl2 H3C PCC CH2Cl2 4. OH НО" CH3
help with all of them please
1) Complete the following reactions OH H2SO4 (a) (b) OH H2SO4 (c) H2SO4 heat heat OH heat ОН H.CO d) HỌCrO, H2C104 e) -OH OH 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.
(16) Predict the organic product(s) in the following reactions(4 points each): مت PCC CH,C12 (b) NaBDA H2O нас. OH + pyridine CH3 CH3 KCro OH НАС H2SO4, H,0 (e) CH SNa H3C. Сна THF CH3
Explain this order of reactivity. Vrite a mechanism for the following reaction. cat. H,804 CH,OH OCH in the course of the following reaction:
(a) 2 1. -OH, H2O H 2.H307, heat (b) CI AICI: (c) SH HS H2SO4 (d) OH 1. Na Cr 07, H2SO4 2. SOCl2, pyridine 3. excess (CH2CH2)2NH excess (e) (f) Br2, H30*