PLEASE ANSWER ALL OF THE QUESTION (a, b and c)
PLEASE ANSWER ALL OF THE QUESTION (a, b and c) Show how you could synthesize the...
Show how you could synthesize the following products via a
Williamson ether synthesis (i.e. select an appropriate nucleophile
and electrophile to react together). Include any reagents that
would be necessary for the reaction to occur (i.e. acid or base).Do not include mechanisms
3. Show reagents that you could use to prepare the following ether via a Williamson ether synthesis and explain your reasoning.
Please confirm if this is right
Could you confirm if number 4 is correct
Could you confirm if number 4 is correct
(4.) Show how to synthesize this ether, starting with alcohols as the only carbon sources, plus any other necessary reagents: 2. Br (4.) Show how to synthesize this ether, starting with alcohols as the only carbon sources, plus any other necessary reagents: 2g mechanism: Pringet tot 6 2 H. (4.) Show how to synthesize this ether, starting with...
can you solve everything please
Short Answer 7. Show how you could synthesize these compounds from any compound having three carbons or fewer. You can use any regent necessary, but keep to the three carbons. Сн, снен, с-н снен, сн, ск, сн, сн, 8. Give an example of a synthesis that requires the protection of an ketone. You may use any reaction, any organic compounds. You must show the reaction that does the protecting. 9. Give an example of a...
help please
6) What products would you expect to obtain from reaction of T-methylcyclohexanol with the following reagents? 4) HIBI b) Na Cro oxidizing agents) How would you prepare the following ether using a Williamson synthesis?
Starting with acetylene use a sequence of reagents to show how you could make each of the following products. Note that some steps will be redundant so please just start from a common intermediate once you have shown its synthesis. For example, all of the other products can be made from either 1-butyne or 2-hexyne. You may not use any other source of C other than methyl bromide, calcium carbide, chloroform and the products you can make from these sources....
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?
5. Show how to synthesize the following molecules using the given starting material. Show all the intermediate products for multiple steps. You can use any other reagents or starting materials necessary D amer --
Please show all steps and include how to
determine the equivalents needed
The final step in the synthesis of naproxen (the active ingredient in the commercial painkiller Aleve) involves a Williamson ether synthesis. Propose a mechanism for the transformation shown below. Include all charges and intermediates and stoichiometric equivalents of each of the reagents used (i.e. 1 equivalent, 2 equivalents, excess, etc...). [3 Marks] OH DY" – 6607 naproxen
Please answer and show all work. It is a multistep
question.
[1]. How do you prepare the following compounds, starting from benzene? These synthesis require multiple steps, show all reagents and intermediate products CO2CH3 b.COM CH,CH3