Give the complete synthesis 45. b) Give the complete, detailed synthesis for the following structure. You...
Draw the complete synthesis of the compounds Question 44 (10 points) Pick One! Draw the complete, detailed synthesis of one of the three compounds below on your paper. You may use benzene, cyclohexane, or cyclohexanone as one of your starting compounds. You can use any monofunctional organic compound with one or two carbons. You can use any inorganic reagents of your choice. Up to 3 points will be awarded for each additional synthesis problem done correctly. (10 points) < Paragraph...
Please answer the question completely. 10. Propose a synthesis for two of the following molecules. You may start from any compound of 3 carbons or fewer, and usc benzene, acctylenc, and any functional group as a starting material to make the final product as shown. You may use anly reactions you choose. (15 points each): على علیہ تعمل اللہ تہ
5. Give the reactions for the following synthesis using benzene and any inorganic reagent. OEt steps HO 6. Give the reactions for the following synthesis using and two carbon functional group and any inorganic reagent. (hint: use Wittig and Gilman reactions) steps ОН —
5. Give the reactions for the following synthesis using benzene and any inorganic reagent. t LOEt ot steps , ropo HOA steps / 6. Give the reactions for the following synthesis using and two carbon functional group and any inorganic reagent. (hint: use Wittig and Gilman reactions) LOH _ steps HO
can you please solve everything 9 Give an example of a synthesis that requires the protection of an alcohol. You may use any reaction, any organic compounds. You must show the reaction that does the protecting. Acetylide ion reacts with cyclohexanone, followed by acid workup. Write a complete mechanism. 10. Identify the compound that gives this NMR spectrum. The compound has carbons. 11. 4
Please explain the mechanisms! 1. Propose a synthesis for each of the following problems starting with reagent shown and using any other organic or inorganic reagents allowed in each problem. Multiple steps are required. The number of steps you use does not matter. Reactions should give the desired product as a major product. For full credit show the product of each step (reaction). If you make use of organometallic reagents such as Grignard, Wittig, organolithium, organosodium, organocopper, etc. you must...
One-step synthesis: Design a synthesis, showing all of the reagents and products along the way. You may use any inorganic reagent and any organic reagent of two carbons or less. 3) НО. НО ? + En
Devise a stepwise synthesis for the compound below using any of the following reagents: cyclohex-2- enone, alcohols, alkenes, and/or alkynes of FOUR carbons or less, benzene, any inorganic reagents, any oxidizing or reducing agents, and any peroxyacids. DO NOT GIVE MECHANISMS. (Bonus: make your cyclohex-2-enone using only the other reagents given) он Devise a stepwise synthesis for the compound below using any of the following reagents: cyclohex-2- enone, alcohols, alkenes, and/or alkynes of FOUR carbons or less, benzene, any inorganic...
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...
3. 6 pts each - Choose two of the following problems and devise a synthesis to create the corresponding molecules. You may use any reagent or starting material containing 4 carbons or fewer, a phenyl group, or a benzyl group. The third synthesis may be attempted for up to 5 points of extra credit points. ??? ???