starting with benzene prepare each of the following CH3 C2H5 COOH COOH NO2 NOZ NO2 COOH CH3 NO27 N02 COOH NO2
Find the mechanism COOH COOH CH3C1 0=0=o=0 KMnO4 conc. HNO3 Anhy. AICI: heat conc. H2SO4 HO NO2 3-nitro benzoic acid benzene toluene benzoic acid Sn/HCI COOH COOH COOH HO NaNO2 + HCI 0°C COH N CI NH2 3-hydroxy benzoic acid 3-chlorodiazenyl)benzoic acid 3-amino benzoic acid
4. Review from previous chapters Propose a synthesis COOH NO2 COOH var
Starting with benzene prepare each of the fol1wing: CHз SO3H SO3H Br Br NO2 COOH соон CHЗ C2HS c1 NO2 NO2 NO2 CHЗ Соон NO2 NO2 NO2 СОон
9) Draw the product(s) for the following reaction. 3pts 1 eq. HNO3 H2S04 10) Select the product for the following reaction. 2pts Excess HNO3 ? H2SO4 1hr NO2 NO2 NO2 -NO2 B с D NO2 NO2 11) Provide the full mechanism for the following reaction (use as much space as you need). 5pts HNO3 NO2 H2SO4
I know what the final product is, I need help with the reaction mechanism. Please draw and explain reaction mechanism that forms the final product. M) OH 1. Na2Cr207, H2S04 N) 1. PCI 5 S ONa 2 pyridine К) њег M) OH 1. Na2Cr207, H2S04 N) 1. PCI 5 S ONa 2 pyridine К) њег
VI. Synthesis. Use retrosynthetic analysis (12 pts) COOH NO2 Dame
Please draw the arrow pushing mechanism for the following reaction NO2 HNO3 + H2SO4
Give the IUPAC name. CHs HO CI CHO F F COOH NO2 Br
Question 8 What is the major organic product obtained from the following reaction? COOH OOOH COOH COOH COOH -NO2 HNO, H2SO4 "NO2 Br Br Br NO2 2 Br 4 3 1 a. 1 b. 2 C. 3 d. 4