Please show steps Show how to prepare the following ether from methylenecyclohexane using the alkoxymercuration reacti...
How would you prepare benzyl methyl ether using a Williamson ether synthesis? The list of reagents to choose from are: 2-Chloro-norborane, Benzyl chloride, 2-Chloro-2-methylpropane, 4-Chloro-1-butanol, and Chlorobutane. I was reading online and it kept mentioning SN2 reactions, using an alcohol, and an alkyl halide for the synthesis. My guess would be using Benzyl Chloride and another one with an OH attached, but I could be completely wrong. Please help and explain by showing the reaction mechanism. Thank you so much!...
please be detailed
Bonus. Provide a sequence of synthetic steps to prepare ether B from 2-methyl propane A: (10 points) HEC CH3 HC H3C CH3 CH3
How can I prepare Propyl Benzhydryl Ether using William ether synthesis? I have to use diphenylmethanol as a starting material. Please provide me the whole procedure with the appropriate steps and amount of substances I need to use. Thanks!!
(2) Show how you would prepare the following Compound from benzere include all reagents and intermediate structures Show all steps in mechanism for this reaction HCI CH3
Show the detailed synthesis of the following compound from
but-1-ene. Show the steps in the correct order, with numbers
identifying the steps, the necessary conditions and showing
intermediate reaction structures. It is not necessary to show the
reaction mechanism.
Н.С нс- -ОН
3. Show reagents that you could use to prepare the following ether via a Williamson ether synthesis and explain your reasoning.
Please show steps and explain
(8) 5. Prepare the following compounds using nucleophilic substitution and eliminations. Start with alkyl halides, alcohols, thiols, etc., and inorganics. Any common solvent is allowed. a) CH NH2 b) CH, CHCH 0-CH, CH
2.How will you prepare the following reaction using Wittig Reagents. List all the steps from the alkyl halide. ( 4points)
Please show me the steps and arrows for every step
If you can also explain to me why
Thank you very much.
1.) What is the mechanism and main product for the following reaction? (5 points) OH + ~ -- Na
please answer question number
Questions: 1. Show, by equations, how you would prepare phenylbenzyl ether by the familiar Williamson synthesis. 2. In the preparation of methyl-2-napthoxy ether: A. What substances are present after the final reflux period? B. What serves as the nucleophile? C. How is the product purified? 3. In your preparation of 2,4-dinitrophenyl-p-tolylamine: In A. How is excess amine removed from the product? B. What serves as the nucleophile?