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Fill in the missing reagents that would give the target molecules. These transformations will require more...
Synthesis version: 7. Provide reagents for the following two transformations. If more than one step is required, number individual steps. Use your answers to 6a and 6b to help you with this! Br CH,CH3 + E H CIWC- H, OH HzC CH3 CEC CH,CHz . HC Br H C-CICH "CH + E HO CH2CH3
6. Fill in the missing reagents for the following reactions. If more than one step is necessary, indicate according Br (racemic) OH (racemic) Br (racemic) 7. Synthesize the following molecules by providing the correct substrates and/or reagents. Br Br Br
(10 pts) Fill in the missing intermediates (two), final product, and reagents (two) in the llowing multistep synthesis. Br X OH -- NH 에 CH,Br 6) (5 pts) Write out the 3-step arrow pushing mechanism showing how cyclopentanol is dehydrated to make cyclopentene: он conc. H,SO + HO heat
Question 5 (27 pts.) Synthesize the target) molecules on the right from the starting molecules the left. this can not be done in one reaction. Give reagents and conditions and the intermediate molecules at each step. Do not show any mechanisms or transient intermediates. If other isomers are formed at any step then you need to indicate this but you do not need to draw their structures. NOZ CO2H SO3H
Question 5 (27 pts.) Synthesize the target) molecules on the right from the starting molecules the left, this can not be done in one reaction. Give reagents and conditions and the intermediate molecules at each step. Do not show any mechanisms or transient intermediates. If other isomers are formed at any step then you need to indicate this but you do not need to draw their structures. NOZ CO2H SOH
2. How will you carry out the following transformations? Give reagents and products for each step clearly. the Libri Heze-luze - HC=C - CH₂ CH3 do BRL Br e told cott HO tc-lt
Problem IV. Synthesis (24 points). These transformations will require multiple steps. Provide the reagents for each step and draw out your proposed synthetic intermediates. Please do not draw curved arrows; this prob- lem is not asking for mechanisms. You do not need to provide solvents for the reactions. (1) (12 points) Provide a synthetic route-i.e., a sequence of reactions-to produce compound SS from compound RR using any other starting materials and reagents you wish. RR (2) (12 points) Provide a...
6. (20) Fill in the missing reagents to accomplish these conversions (>1 step may be needed): 7, (10) Give the alkyl halide which would give only the alkene shown by way of an E2 elimination (one alkyl halide for each alkene): 8. (10 - extra credit) (a) (6) Propose a 2-4 step mechanism to explain this conversion. (b) (4) Draw a reasonable reaction coordinate diagram for this process.
1) 2 (CH3),CHCH Br / Cul/ 4 Li? CHỊCH, CHỊCH 2) H30+ 2. Using any necessary reagents, show how the following synthetic transformations may be achieved. Give reagents and conditions for each step. Include all synthetic intermediates compounds produced during the course of multi-step synthesis). NOTE: You may not use HOC OH 1. For each of the following questions, provide the missing reagents that can be purchased) and conditions or predict the MAJOR product. Indicate stereochemistry and identify a racemic...
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6) Fill in the missing reagents and intermediate products for the following two step, EAS reaction. (6 pts) SO, 7) Draw the two neutral starting materials needed to generate the products via an S2 reaction. A base may be needed to complete the reaction, but it does not need to be included. More than one option may exist, but only draw ONE pair of molecules. (6 pts each) b) 8) Fill in the starting materials in this...