11. Provide the reagents for the following synthesis below (Hint: Be careful of going from B...
Provide the proper order, steps, and reagents used for the
synthesis of the product below from benzene.
IV. Synthesis: A) Provide the proper order, steps, and reagents used for the synthesis of the product below from benzene. SOSH
1. Provide a complete retrosynthesis and forward synthesis of the target molecule below from the given starting materials. All carbons of the target must be from the given starting materials. You may use any reagents you find necessary. You may include more than one step over a reaction arrow, but please no more than 3 steps at a time. Please show the key intermediates in your synthesis for partial credit. (10 bonus points) For full credit, include a retrosynthetic analysis,...
b. Complete the synthesis shown below using any reagents of four carbons or fewer. (Consider: Robinson) [6 points]
11. Propose a synthesis for each compound below. You must write in all necessary reactants, reagents, and solvents to receive full credit. Your starting materials must be 3 carbons or less. If you use an ionic or organometallic species, you must show how it was synthesized from a neutral, covalent species. Any species that adds carbon to your product must be synthesized from a molecule of 3 carbons or less. Only show the steps of your synthesis- do not put...
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...
How would you carry out the synthesis below? Additional
carbons may come from any alkyl halide with 3 C's or less. Show the
reagents needed for each step of your transformation, but do NOT
draw the mechanisms for each step.
SHORT ANSWER #30: How would you carry out the synthesis below. Additional carbons may come from any alkyl halide with 3 C's or less. Show the reagents needed for each step of your transformation, but do NOT draw the mechanisms...
8) Suggest a synthesis for the following comp neccesary reagents. Provide the structure of all key compounds in the synthetic route.(16 Points) ounde from the provided starting material. You may any dr a) Br b)
mation shown below requires at least two steps. Provide the reagents/conditions for each & Each transformatie transformation. (20 pts) Reagents A-? Reagents ? Reagents D? Reagents .....: Reagents ? 6. Predict the product from the Birch reduction shown below: (3 pts) N2, NH3 CH, OH Bonus: (6 pts) Provide a synthesis for the target molecule using benzene.
Complete the following synthesis by selecting from the list of 10 reagents below. Each reagent (or set of reagents) is labeled as a letter. In the answer box, simply place the order of reagents used as uppercase letters. For example, if your synthesis involves using reagent A followed by B, followed by C, and then D, your answer would be: ABCD. NaOH NaOET 1. NaBH4 ext H2O EtOH 2. H20 A B с D E Br H30+ Ph3P=CH2 PCC heat...
Complete the following synthesis by selecting from the list of 10 reagents below. Each reagent (or set of reagents) is labeled as a letter. In the answer box, simply place the order of reagents used as uppercase letters. For example, if your synthesis involves using reagent A followed by B,followed by C, and then D, your answer would be: ABCD. 0 NaOEt 1. NaBH4 NaOH H20 EtoH 2. H20 heat нзо Ph3P-CH2 PCC heat Enter Your Answer: