Show full reaction mechanisms and products, explain reactivity AlCl3 AICI:
2. (6 points) Show full reaction mechanisms and products, explain selectivity: HNO3 H2SO4
aromatic reactivity mechanisms not needed only products Draw the product(s) of the following reactions HNO/H,SO AICI SOY/H2SO4 Bry/FeBry HNO/H,80 AICI Bry/FeBry
4. Draw the mechanisms for the followino reartions to nredict the products Clus AICI
Question 2 (a) Predict the products A-F of the following reactions (no mechanisms are required): AICI: Br2 Meo para os 0.0... HF H NMe,, POCI then H30Ⓡ 1. NaNO2, HCI 2. H20 NH2 [6 marks] (b) Suggest a mechanism for the following reaction: ОН ano [4 marks] [Total for question 3 = 10 marks]
I want mechanisms for the this reactions (Diels-Alder cycloaddition reaction ) ,with explain steps , please I want a clear pic. ? Table 1. [AlCl3 + 2THF]-Catalyzed Diels-Alder Reaction of Ethyl Acrylate (la) with Isoprene (2) under SFC at 30 °C [AICIz + Ln] 5 mol % SFC, 30 °C, 12 h VIPT:. Scheme 2. [AICI; + 2THF]-Catalyzed Diels-Alder Cycloadditions of la with 1,3-Butadienes 4 and 5 at 30 °C [AICI: +2THF] 2.5 mol % SFC, 45 °C, 6 h,...
please show the mechanisms for d-i Chapter 14: Carboxylic Acids Please Show Reaction mechanisms (d) 1. H.Cro 1. BH3 2. H,O, HO Na o 2. NaOH NaOH e) H2 OH ОН CH,COOH H Pt 1. BH; HACO () HO 2. H.O., NaOH SOCI HO O R R RCI Cl2 HẠCrO4 19 AICI: AICI: OCH OH CH,OH H RCI used in the first reaction cannot be a tertiary alkyl halide. (h) heat ОН OH H2CO (1) OH 1. LAIH Lo La...
Provide a full mechanism to account for the following reaction: (5pts] AICI:
II. REACTION MECHANISMS Provide plausible arrow pushing mechanisms to explain how products are formed. WATCH THE DIRECTION (Nu- to E+). The hydrogen bond will NEVER (as in NEVER) move on its own. Make sure the arrows are clear so I can see them as a PDF file
draw final products, mechanisms and intermediates c) 1. CH3CH2CI, AICI: 2. KMnO4 3. SOCl2, pyridine 4. H2N-CH2CH3 , pyridine 5. LiAlH4 6. H307 workup
Use curved arrows to show the mechanisms of formation of the substitution products in each reaction. Indicate stereochemistry of the products where necessary. [10 points] OCH3 а) DMSO Br H CH3CH2ОH b) Br NaOH c) THF