Synthesis question. Show how the starting material can be converted to the product through any of the reactions you have learned in OChem 1 and OChem 2. Show all the reagents you need
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- synthesis question: show how the starting material can be converted to the product through any of the reactions. Show all the reagents you need and indicate the stereochemistry when appropriate. If a racemic mixture is formed, draw both enantiomers and write "racemic "next to the two structures. You don't need to show arrow pushing like a mechanism question. Only the reactions. All carbon atoms in the products should come from the starting material. Use as many molecules of the starting material as you might need to get the productDraw the final product of this series of reactions. |||** OH 1. SOCI₂ 2. NaCN • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • If more than one product is possible, only draw the major product. • If the reaction produces a racemic mixture, draw both stereoisomers.Curved arrows are used to illustrate the flow of electrons. Follow the arrows and draw the intermediate and product in this reaction. Include all lone pairs. Ignore stereochemistry. Ignore inorganic byproducts. Draw Intermediate CH₂OH₂* protonation H₂C CH3OH₂* protonation CH3OH deprotonation loss of H₂O elimination Draw Intermediate CH₂OH nucleophilic addition || Draw Intermediate CH3OH deprotonation Draw Product
- 3. Identify all stereocenters in the following molecules as R or S. Joni NH₂ H 4. Consider the following reaction. This reaction is a multi-step reaction. [1] Draw the mechanism for each step of this reaction using curved arrow notation, include all lone pairs of electrons if they are directly involved in the reaction. [2] Identify the arrow pushing pattern (mechanistic pattern: nucleophilic attack, loss of leaving group, or proton transfer) for each step. [3] Draw a transition state each step. H-OSO3H H CH3 | Хо-сно H3C-O-H + H3C-O-H H This content is protected and may in shared distributedTwo step syntheses: Draw the major product of each step. If the starting material includes a chiral center assume it is a racemic mixture ( explain well with step by step answer ).A Moving to another question will save this response. Question 6 A natural product having [a]D = - 40.3° was isolated and purified .This information indicates that the natural product O A. is dextrorotatory. O B. does not rotate plane-polarized light. Ocis levorotatory. O D.Meso compound O E. is racemic. A Moving to another question will save this response. Type here to search 立
- Show how you would synthesize the target compound ne right from the starting compound on the left. Show reagents and conditions, and the structures of important intermediate compounds. Do not show any (arrow pushing) mechanism. Ignore stereochemistry in this question.Given the general reaction coordinate diagram for an El reaction, what does the 1st transition state refer to? TS E TS, SM Reaction Coordinate An activated complex between the leaving group and carbocationic species. An activated complex between the nucleophile and carbocationic species. None of these O An activated complex between the base and carbocationic species.Check all the true statements regarding the reaction shown here. C H CH3SLI This reaction will require more than two mechanistic steps. A mixture of chiral and achiral organic products is expected. This reaction will yield exactly two stereoisomeric products. This reaction will yield more than three stereoisomeric products. This reaction will take place in one step. All the organic products will be chiral. This reaction will yield exactly one organic product. This reaction will take place in two steps. All the organic products will be achiral.
- For the given molecule, highlight any nucleophilic sites in red and any electrophilic sites in blue. XAlkene bromination. The two butane isomers react with Br2. Draw the key reaction inter- mediates and the product(s); use arrow pushing to explain the stereochemical outcomes of the reactions Final Products Intermediate Br2 Intermediate Final Products Br22. Show how you would synthesize the target compound on the right from the starting compound on the left. Show reagents and conditions, and the structures of important intermediate compounds. Do not show any (arrow pushing) mechanism. Ignore stereochemistry in this question. To preview image click here Br HO HO