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For each problem, design a synthesis, showing all of the reagents and products along the way....
Please write neatly, thank you. INSTRUCTIONS: I'd recommend answering these on a separate sheet. Make sure to label your answers clearly with each problem number. For each problem, 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. ONE STEP SYNTHESIS (20 points]. Choose any FOUR of the five problems below to answer. (Answers beyond the fourth do not count.) 1) 3)...
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
Please go through each step of this synthesis problem and show each reactant bwtween steps! It is very important that they are correct so please make sure your answer is right! thank you so much! E. SYNTHESIS: (12 points) cohols, alkenes synthesize the molecule below using any of the following reagents: a and/or alkynes of three carbons or less, any inorganic reageAts, any oxidizing or reducing agents, and any peroxyacids. DO NOT GIVE MECHANISMS. HO OH HO
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...
Multistep Synthesis (9 pts) Show how to convert benzene into at least one of the molecules below using any reagent. You should be able to do this in three steps but this is not a required minimum or maximum. If you are not sure of an intermediate step put down structures and as much as you know about reagents to maximize partial credit. You may attempt more than one and the best will be graded. It is ok if a...
Synthesize the molecule below using any of the following reagents: cyclopentane, alkanes, alkenes, or alcohols of three carbons or less, any inorganic reagents, any oxidizing or reducing agents, and any peroxyacids. show each intermediate and the reagents needed for each step. E. SYNTHESIS: (15 points) Synthesize the molecule below using any of the following reagents: cyclopentane, alkanes, alkenes, or alcohols of three carbons or less, any inorganic reagents, any oxidizing or reducing agents, and any peroxyacids. Show each intermediate and...
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. ??? ???
#19 all 6 synthesis Design a synthesis of each target using the starting material and any reagents containing three carbons or less. Read the assigned pages in the text, and do the assigned problems
Please answer question 4 with a full explanation. 4. (9 points) Multi-step synthesis. Devise a synthesis for the target molecule starting from benzene and small alcohols with no more than two carbons. You can use any inorganic reagents necessary target 5. (10 points) Analysis of 'H NMR spectrum. Below is the 'H NMR spectrum of the product from this week's experiment.
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 a:s 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 Question 10 но но OCH3 н,so TMS-C РСС Li 2. H20 H20 Et3N H-Br OCH3 CH3OH 1. NaH TBAF 2....