Write the background information on
Willoamson Ether Synthesis 1 and 2
Amine formation
Write the background information on Willoamson Ether Synthesis 1 and 2 Amine formation
please answer these questions. thanks 1. Write a reaction of the Williamson Ether synthesis of your product. 2. In this acid catalyzed reaction, a stable benzylic carbocation is formed. Show how this carbocation is formed. 3. Write resonance forms for the benzylic carbocation that is formed. 4. Use the government website www.uspto.gov to find the patent number for the synthesis of your product. Step 2: Ether Synthesis он OR NaBH ROH Amberlyst-15 NaoH H,O он он он
write an equation for the formation of dimethyl ether from methanol
write the mechanism for the williamson ether synthesis of 1-ethyl-4-propoxybenzene from 4-ethylphenol and 1-iodopropane.
5. Write the corresponding letter according to the following selection: A) Ester, B) Ether, C) Amine, D) Amide, E) Aldehyde (CH3)3N CH3OCH, CH2=0 CH3NH2 O=CHNH2 CH3CO2CH3
1. A common problem in the acid-catalyzed hydration of alkenes is the formation of an ether byproduct. Show the formation of the ether byproduct in relation to the reaction below by providing a curved-arrow mechanism for its formation. (2 pts) H307 Но + 0 OH
pls help Testdents are trying to synthesize the same ether thatuned two different products Compounds A & B. 2 points) Gave stretures for compounds A&B. S a ints) Write mechanisms to account for the formation of each product. 0 Na Shorm o synthesis is the formation of 1. Na Compound A Bonnie's Sms Sannie Sie 2014 HONE? Compound B CO- Na Two students are trying to synthesize the same ether. But they obtained two different products Compounds A & B....
Reductive Amination Write down a reaction scheme for the synthesis od N-benzyl alanine methyl ester hydrochloride. (Reagents are methyl pyruvate, benzylamine, sodium triacetoxyborohydride) Maybe helpful: Scheme 1:Formation of an N-substituted imine(Shiff base) through the reaction between a carbonyl-containing compound and a primary amine Scheme 2: Imine reduction yields an amine
Friedel - Craft Acylation Synthesis of 4-Methoxiacetophenone Background Information 1.- What is an electrophilic aromatic substitution? 2.- Give three examples of activating groups. Explain why they activate the ring for substitution. 3.- Give three examples of deactivating groups. Explain why they deactivate the ring for substitution. 4.- Describe the difference between a Friedel-Craft alkylation and Acylation. Synthesis of 4-Methoxiacetophenone For this Friedel-Craft acylation we will react Anisole with Acetic Anhydride. Write the mechanism and the structure of the final product....
Propose a synthesis of the following amine from ethanol. Ethanol should be the only carbon source you use. 1.) Propose a synthesis of the following amine from ethanol. Ethanol should be the only carbon source you use. T OH 2) Propose a synthesis. I он 3) Propose a synthesis. I
Which of the following reactions is classified as a Williamson ether synthesis? d) Which of the following reactions is classified as a Williamson ether synthesis? A) CH3OH/ Δ B) 1. Na 2. CH3CH2I C) 1. CH,MgB:/ ether D) 1. Hg(OAc)2/ CH3OH 2. NaBH4 E) 1. MCPBA