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
Show how you could synthesize the following products via aWilliamson ether synthesis (i.e. select an...
PLEASE ANSWER ALL OF THE QUESTION (a, b and c) Show how you could synthesize the following products via a Williamson ether synthesis. Include any reagents that would be necessary for the reaction to occur.
3. Show reagents that you could use to prepare the following ether via a Williamson ether synthesis and explain your reasoning.
Show how you could synthesize the products below using a Grignard reagent and appropriate electrophile by drawing the overall balanced equation. No mechanisms are required for this question. You do not need to show formation of the Grignard reagent. [2 marks] HO H3COH Ph Phi
Show how you could synthesize the products below using a Grignard reagent and appropriate electrophile by drawing the overall balanced equation. НО не он PhPh.
Alkoxide ions react with haloalkanes, or alkyl halides, forming an ether. The generic reaction is RO:1 + R'X → ROR' a) Draw or write the structure of an alkoxide ion and a bromoalkane that can be reacted together to synthesize 2-methoxy-2-methylpropane, (CH3)3COCH3. b) Draw or write the structure of the alcohol that can be deprotonated to form your alkoxide from part 'a'. c) What base would you use to deprotonate the alcohol from part 'b' in order to convert the...
4. Synthesize the following compound from starting materials containing the indi cated number of carbons. Show your syntheses in the forward direction and include any necessary reactants, reagents or catalysts. Do NOT provide mechanisms. (25 pts) 4. Synthesize the following compound from starting materials containing the indi cated number of carbons. Show your syntheses in the forward direction and include any necessary reactants, reagents or catalysts. Do NOT provide mechanisms. (25 pts)
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...
1) Predict the major product in each of the following transformations. Show the mechanism. 2) Show how you could synthesize the products below using a Grignard reagent and appropriate electrophile by drawing the overall balanced equation. Include the mechanism. Predict the major product in each of the following transformations. No mechanisms are required for this question. [3 Marks] 1. CH,сн,МgBr (еxcess) 2. HС{aq) 1. PhMgBr (1 equiv.) 2. HCI(aq) ОН HO 1. CH2MgBr (2 equiv.) 2. HCl(aq) Н Show how...
① ( 38 Points) Synthesis for the cases below show how you would synthesize the desired product from the given starting material using any Reaction in Chapters 1-9, Use any recessary Reagents and any alcohol up to 6 carbons H-C=C-17 myh Acetylene Starting material heptanal starting maker
20% Multi-Step Synthesis Sa) Show how you could perform the following synthesis. You may use any reagents that you need. 20% Multi-Step Synthesis Sa) Show how you could perform the following synthesis. You may use any reagents that you need.