3) Identify the reagents that you would use to produce the following compounds using a Claisen...
22.30 Identify the reagents that you would use to produce each of the following compounds using a Claisen condensation: OEt OEt
identify which compound is more acidic and explain your choice. or each of the following compounds, Make sure you include structures of these which compounds in your answers ounds, 1. F (e) 24-Dimethy-3,5-hepanedione or 4, 4-Dimethy)-3,5-heptanedione (b) 1.2-Cyclopentanedione or 1,3-cyclopentanedione 2. When 2-hepten-4-one is treated with LDA, a proton is removed from one of the gamma (z) positions. identily which gamma position is deprotonated, and explain why the y proton is the most acidie proton in the compound. 3. Rank...
0 2.) Predict the product of each of the following reactions. Practice writing the mechanism (+1 point bonus/problem). 0:0 1.)LDA 2.) O o 3.) H2O* eagents that can be used to produce the following compounds by an aldol reaction. 3.) Identify reagents that 1) No он a.) HO
3) The following compounds can be made by either an Aldol or a Claisen condensation. In each case, indicate whether the product is as result of an Aldol or a Claisen condensation AND then draw the appropriate starting material(s) that would be used to form the product. OEt (B) (D) O Et
5. Identify the reagents you would use to convert cyclohexanone into each of the following compounds NOZ 6. Draw a plausible mechanism for the following transformation:
1. Which of the compounds listed below would produce the following aldol condensation product? 2. Which is not a product of the claisen condensation of ethyl ethanoate and ethyl butanoate? 3. A claisen-schmidt reaction shown below, is an important step in the commercial synthesis of Vitamin A: what type of reaction is the claisen- Schmidt? 4. Which of the following statements is true about the anion formed from the reaction of diethyl malonate with sodium ethoxide? please help A. cycloh...
(6 points) Identify what reagents you would use to synthesize the following compound with a Robinson annulation reaction: (6 points) Propose a reasonable step-by-step mechanism for the following conversion: NaOH jd met H2O
14. (6 points) Identify what reagents you would use to synthesize the following compound with a Robinson annulation reaction: 15. (6 points) Propose a reasonable step-by-step mechanism for the following conversion: Get morgon 3.1
1. a. Provide the reagents necessary to produce the following products, or b. One of these products forms preferentially at low temperature, the other at high temperature. Explain. 2. Propose structures for compounds B and C for the following reactions. Indicate the mechanism for the formation of compounds B and C. NaOCH2CH3 CHCHCHBr H2O+, A B A
please help in all sections asap!! Which of the following reactions would produce isopropylbenzene as the major product? ОН AICI: H2SO4 H2SO4 AICI3 IV I all of these Predict the product for the following reaction fuming H2SO4 SO3H Predict the structure of the major product for the following reaction Which of the following compounds will not undergo nucleophilic aromatic substitution? 1-chloro-2,4-dinitrobenzene 1-bromo-4-nitrobenzene O-chloronitrobenzene m-chloronitrobenzene p-chloronitrobenzene Choose the correct sequence of reagents for the following transformation. 2) 3 . NH2 2)...