1. 2. a. b. Provide the major organic product of the following reactions. a. b. 1. Mg, ether 1. Mg, ether 2 2. CO2 H 3. Dil. H 3. Dil. Ht Provide the missing reagents. OH 6-8
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- ( give mechanism of 3 and 4Which compound is not a possible product in the reaction below ( F2 is in excess F2and UV light the catalyst).CHA + F2 -->O CFAO CHFaO CHF-O CH2F2O CHaFII. Alcohols in Synthesis B.) How are alcohols used to make ethers in the Williamson ether synthesis? How do you design the synthesis of ethers using both acidic and basic Williamson ether synthesis strategies?
- Given this organic synthesis, is there any limiting and excess reagents? also describe the procedure is run, how is the reaction monitored?Is the order fo addition important? N-ETHYLALLENIMINE[Aziridine, 1-ethyl-2-methylene-] Submitted by Albert T. Bottini and Robert E. Olsen1.Checked by Thomas H. Lowry and E. J. Corey. 1. ProcedureCaution! This preparation should be carried out in a good hood to avoid exposure to ammonia. The operator should wear rubber gloves and protective goggles because 2-haloallylamines and ethylenimines can cause severe skin and eye irritation. A 2-l. three-necked flask is fitted with a sealed mechanical stirrer, a gas-inlet tube, and a dry ice condenser protected from the air by a soda-lime drying tube (Note 1). The system is flushed thoroughly with dry ammonia, and 32.8 g. (0.84 mole) of sodium amide (Note 2) is added to the flask. The system is again flushed with ammonia, the condenser is provided with dry ice covered by acetone, and 1.2 l. of liquid…Please could someone with Chemdraw software create the mechanism for wittig reaction with these reagents. Thank youFor butenafine, develop a synthesis that starts with napthalene and benzene. (aromatic methyl groups can be converted to alkyl bromides using Br2/light, and aldehydes by heating the alkyl bromide in DMSO, eg. ArCH3 to ArCH2Br then to ArCHO).
- A. Give a product that contains carboxylic acid found in the market. Name of product Carboxylic acid present and its uses B. Give a product that contains ester found in the market. Name of product Ester present and its uses I WILL UPVOTE BUT PLS BE INFORMATIVE, THANK YOUUUUsing any necessary organic and inorganic reagents, show how you can carry out the chemical conversions shwon below. Please answer parts a, b, and c.Arrange the structure on the image with regard to the reactivity towards hydrolysis. 1 being the least and 3 being the most
- A. Provide the necessary reagents. B. Provide the necessary eragnets and the step by step mechanism.Given the sequence of reactions shown below assume the reactions are stoichiometric fill in the reagents needed for steps A B and C and explain what happens in each step of the reactions, by also nameSynthesize 3,5-dibromotoluene from benzene and any suitable inorganic and organic reagents. Assume you CANNOT separate ortho and para products and both isomers have to be carried through in the entire synthesis.