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Please show the reagents and mechanism for the bottom one. Thanks! Outline practical laboratory, steps, showing...
Q: Draw out the mechanism. Please show all steps so I can understand. Thank you! arrow formalism to describe how the reaction below occurs. Be sure to draw out all reaction intermediates & the movement of all electrons needed to justify the formation of the indicated product. You do not need to add in any reagents that are not shown OR show any other products that could be made but are not shown (focus on showing the mechanism for only...
Mechanisms: Outline a detailed mechanism for each of the following. No other reagents than those given are necessary. Use arrows to explain the flow of electrons and show all intermediates. - On Mechanisms. Outline a detailed mechanism for each of the following. No other reagents than those given are necessary. Use arrows to explain the flow of electrons and show all intermediates. 17. Br2 OH + HBr O my te mos ek.no H30+ HO. + H2O
Outline all steps in the laboratory synthesis of the following compounds from benzene and/or toluene, using any needed aliphatic or inorganic reagents. Assume the para isomer can be separated from an ortho,para mixture. Do not show mechanisms. p-bromobenzoic acid m-bromobenzoic acid 2-bromo-4-nitrotoluene 2-bromo-4-nitrobenzoic acid 4-bromo-3-nitrobenzoic acid o-iodobenzoic acid
Show the complete mechanism for the following transformation. Then, show the reagents and intermediate steps to complete the synthesis. CF3 CF3 ??? O2N o X steps ZI
Hi there. Could you please show a stepwise mechanism for the following: Please SHOW ALL STEPS so I can understand. Thanks! :) (a) 2-methylcyclohexanol dehydrating via El pathway to form the major product detected by GC (b) cis-2-methylcyclohexanol dehydrating via E2 pathway to form the major product detected by cyclohexanes to illustrate this mechanisms stereochemical requirements.
Please explain along with showing the mechanism. I am thinking this one has to do with the reaction favoring x due to better carbocation stability but I am unsure. 7. (10 points) Under the reactions conditions below, product X is formed exclusively. Provide a mechanistic explanation for the regiochemical selectivity of this reaction. OCH3 CH3OH H2SO4
1. Use standard conventions to write a mechanism for the reaction sequence below and provide an unambiguous structural formula for the organic product o cerere min Excess CH3CH3MgI to H20+ 2. Show the reagents and/or conditions one could use to convert propanoic acid into N,N-dimethylpropanamide. More than one step may be required. 3. Show the reagents and steps one could use prepare ethyl acetate assuming alcohols are the only source of carbon
NEED HELP WITH ORAGNIC ASAP! NEED STEP-BY-STEP REASONING AND EXPLAIN EVERYTHING.MUST SHOW ALL WORK AND STEPS PLEASE AND SHOW STEREOCHEMISTRY FOR EACH REACTION!!! (PLEASE DONT REPOST OLD ANSWERS) The (-------) lines indicate unspecified steriochemistry please identify those!!! And show all intermediate via arrow pushing.PLEASE DO 2A AND 2B! 2A)- Indicate reagents and approximate reactions conditions that could be used to effect the following transformations. In the process, show each step of the reaction including resulting intermediates giving rise to the...
Provide a mechanism for the following reaction. Please show all intermediates and use arrows to show the movement of electrons. Propose a synthesis for the following compound. You may use any reagents needed. Complete the synthesis in 4 steps or less (more than one step is needed).
Show reagents and experimental conditions you might use to convert 3-methyl-1-pentyne into each of the following. Please show and explain all steps! 2. Show reagents and experimental conditions you might use to convert 3-methyl-1-pentyne into each of the following: Br