N H OH H2O OHO Ising hromobenzene, cyclohexene and vinyl bromide as your source of carbons,...
5. Using bromobenzene, cyclohexene and vinyl bromide as your source of carbons, outline a synthesis of 1-cyclohexyl-2-phenylethanol which is used to reduce irritation in transdermal drug delivery (15 pt)
5. Using bromobenzene, cyclohexene and vinyl bromide as your source of carbons, outline a synthesis of 1-cyclohexyl-2-phenylethanol which is used to reduce irritation in transdermal drug delivery (15 pt) By o 7or -
Name 4. Starting with cyclohexene and acetylene as the only source of carbons, show a synthesis of the compound below. 1. Show how you could make the given product from the given starting material. Show all steps. OH a CECH 2. Starting with acetylene and methyl bromide as your only source of carbons show a synthesis of cis-2-butene. 5. Prepare 2-methoxy-propanol from 1-bromo-propane. Show the steps and use any reagents you need. 3. Using acetylene and propyl bromide as your...
ОН Which of the following compounds are H2O soluble? H2N OH NH2 ОН H N OH A B С. Q Zoom A A B B С D A and B E B and C F A and C G A, B, and C ОН H-N. ОН NH2 O ОН. H-N- ОН А В с
ОН Which of the following compounds are H2O soluble? H2N OH NH2 ОН H N OH A B С. Q Zoom A A B B С D A and B E B and C F A and C G A, B, and C ОН H-N. ОН NH2 O ОН. H-N- ОН А В с
ОН Which of the following compounds are H2O soluble? H2N OH NH2 ОН H N OH A B С. Q Zoom A A B B С D A and B E B and C F A and C G A, B, and C
For each reagent, predict the major product(s). 1) MCPBA n 1) Os04 H OH HO H A. 2) H30* D. 2) NaHSO3/H2O 3. TOM B. Os04 (catalytic), NMO E. KMnO4, NaOH, cold H OH HO H HO HoT F. OsO4 (catalytic) c.) J OH 2) H30+ ????, NaOH <mo ? ????
Question 8! Please and thank you!!
(F) Br2 (G) Methyl magnesium bromide followed by HCI (H) H+, H2O (1) PBr3 (J) NaBH4 followed by HCI (K) SOCI2 (L) m-CPBA (M) Os04 (N) BH3.Me2S, NaOH, H202 (O) Methyltriphenylphosphonium bromide and Base Question 8: Cyclohexanol reacts with chromic acid (H2Cr04) to provide compound A. The above compound A reacts with Methyl magnesium bromide followed by HCl to provide compound B The above compound B reacts with H3PO4 to provide compound C. The...
N -2 H-6 O-5 Balance these equations Soat 02 7503 NH₃ + O2 >Noat H₂O Fe(OH)2 + O2 + H2O → Fe(OH)23 Pa Hu PH₂ +P4 Na Hu toa > H₂O₂ t Na NaSO 4 +C Naa St co
Br DMSO H20 N-Br OH N-H dilute H2SO4 OH h sN1 Nucleophilic substitution. a Proton transfer e J Electrophilic addition b Lewis acid/base i SN2 Nucleophilic substitution f*E1 Elimination c -Radical chain substitution j Electrophilic aromatic substitution g FE2 Elimination d Radical chain addition Identify the mechanism by which each of the actions above proceeds from a the mechanisms listed. Use the letters a j for your answers.