3) The following Grignard reaction is performed: CH,сH, Нас, H2C OH H 1. CH,CH2MgBr in ether...
H2SO4 Heat нас 2 CH-OH H₂ CH-0 2 H3C-OH + H2C CR A C | CH3 0-CH. нас CH3 dimethyl terephthalate 194.19 g/mol d = 1.075 g/mL bp = 288°C isopropanol 60.10 g/mol 0.7855 g/mL bp = 82.3 °C methanol 32.04 g/mol d = 0.7914 g/mL 64.6 °C diisopropyl terephthalate 250.29 g/mol d = 1.076 g/ml (est.) bp > 300 °C (est.) Problem Two. Start over. This time assume A is a solid and 423.6 mg of A was measured...
H2SO4 Heat нас 2 CH-OH H₂ CH-0 2 H3C-OH + H2C CR A C | CH3 0-CH. нас CH3 dimethyl terephthalate 194.19 g/mol d = 1.075 g/mL bp = 288°C isopropanol 60.10 g/mol 0.7855 g/mL bp = 82.3 °C methanol 32.04 g/mol d = 0.7914 g/mL 64.6 °C diisopropyl terephthalate 250.29 g/mol d = 1.076 g/ml (est.) bp > 300 °C (est.) Problem One. Assume 168 uL A and 123 uL B and one drop of concentrated H2SO4 were allowed...
H2SO4 Heat нас 2 CH-OH H₂ CH-0 2 H3C-OH + H2C CR A C | CH3 0-CH. нас CH3 dimethyl terephthalate 194.19 g/mol d = 1.075 g/mL bp = 288°C isopropanol 60.10 g/mol 0.7855 g/mL bp = 82.3 °C methanol 32.04 g/mol d = 0.7914 g/mL 64.6 °C diisopropyl terephthalate 250.29 g/mol d = 1.076 g/ml (est.) bp > 300 °C (est.) Problem One. Assume 168 uL A and 123 ul B and one drop of concentrated H2SO4 were allowed...
OCH3 OH from One route to the synthesis of HO and CH,CH2MgBr is to 1) protect the ketone as an acetal, 2) reduce the ester to an alcohol, 3) hydrolyze the acetal back to the ketone, 4) protect the alcohol as a TMS ether, 5) react the ketone with the Grignard reagent followed by acidic workup to give the desired product. A second route to the desired product would start with the selective reduction of only the ketone to an...
Grignard Reaction 1. Draw your complete reaction, including the formation of the Grignard reagent and the reaction with your carbonyl compound. Below each reagent, write its molecular weight and density (if a liquid). Also write how much of each material you will use in ml (if liquid), grams, and moles. Also include the molecular weight and melting point of your final product. 2. How many moles of Grignard reagent are you synthesizing? What mass of water could fully react with...
Question 11 Predict the product from the following sequence: H OH H30* NBH, CH,OH hcat O (-H20) OH 0 OH (Zand E) H ОН ОН 1 II DI (Z and E) ОН Н H IV OH OAN 3.1 C. DV EU F FS F6 78
8. Identify the major substitution product in the following reaction: Br 7 сH, CH;он. HC H 9. Which halide ion would react the fastest with cyclopentyl p-toluenesulfonate (below) in ethanol/water? What would the final product of that reaction be? OTS 10. Draw a detailed mechanism for the following reaction. Hint: The first step is deprotonation of the hydroxyl group. NaOCH; ~ OH NOCH CH;ОН
Predict the product for the following reaction sequence. Br Mg/ether H_Cro H,00 OH OH А B C D A Provide the product of the following reaction CI CH,CO Na OCH O Na
1. Select the best reagent(s) from the list below to accomplish the following transformations. In some cases, more than one reagent may be required. 3. HSO3(aq) A.HCI B. Br? C. Hg(OAc)/H20 D. BH3 E. H30*/Hz0 E. Hz02 G. Os04 H. Brz/Hz0 NaBH4 J. H2O, in aq NaOH Reagent(s)? NaHSO3 Product CH3 Starting Material сн. Н.c = — сна BR — Br Br CH₂ На сна нс сна HC нас нас н сну нас НАС СНА оfo/Acal НО н а )...
Provide the product for the following reaction І. Br HOCH,CH,OH Mg/ether H2SO, Н,0° 2. H,0 но он ОН он IV он у Predict the product of the following synthesis. 1. Br2, H20 2. NaOH, HO 3. CH2OH, H+ OCH, н,со OCH, A B с OCH OCH OCH, D E Predict the product for the following reaction. OH Acid Catalyst + 25 °C O А D с B