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Q: Propose an efficient synthesis for the following transformation: The transformation above can be…
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- Please label all the steps and reagents with their corresponding letter. Thanks!show all important steps of rxn. (3S,4R)-2-bromo-3-propyl-2- phenylpentane in ch3OH. label arrow, intermediates, and all potential priductsPlease give me the final product following reaction . Feel free to write out each step! thatd be greatly appreciated!
- Can you draw the products that form when 1-butene reacts with; O3, then Me2S OsO4, then NaHSO3/H2O Br2 in H2O Please analyze in detail for each. Also can you please reply fastly?Below is the equation for a nucleophilic substitution reaction and some experimental data. CH3CH2Br + CH3COO- ⇌ CH3CH2CO2CH3 + Br- Rate = k [CH3CH2Br][CH3COO-] Which mechanism would best fit the data?Q. Carry out following conversion. Provide suitable reagents, reaction conditions and also mechanism of the reactions. Do (iii) as soon as possible.
- The synthesis above can be performed with some combination of the reagents listed below. Give the necessary reagents in the correct order. Be sure to consider stereochemistry and regiochemistry.A. NaOHB. mCPBAC. OsO4, tBuOOHD. NaHE. H2, LindlarF. CH3CH2CH2BrG. CH3CH2ClH. NaNH2I. H3O+J. Na, NH3(l)Chemistry please provide the flow of electrons aswell!! thank you! using the starting material (on the left) to determine the sythetic route which will be the most reaosnable and effective to theres none, you have to start witth the begin products to get to finish needed by using the minmium reagents and reactions needed to get to the final productComplete the reactions given below, write down the type of mechanism (SN1, SN2, E1, E2)?
- For which reaction mechanisms—SN1, SN2, E1, or E2—of thefollowing statement true? A statement may be true for one or moremechanisms. Tertiary (3°) alkyl halides react faster than 2° or 1° alkyl halides.1.)How is this reaction is carry out ? Show all the steps please arrows and all the movement of electrons. 2.)Show the Jones intermediaryIn the box to the left of each reaction below, write the mechanism by which it occurs (could be SN1, SN2, or E1, or even 2 of them). Then draw the product(s).