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- Why does the final product has the opposite configuration compared to the reactant? Shouldn’t it form OMs first, then OMs gets substituted by Cl- via Sn2 (the 1st inversion of configuration) then the Cl- gets substituted by OCH3- (the 2nd inversion of configuration? To my understanding 2 inversions = same configurationo chem - please show stereochemistry and break down each step as much as possibleChemistry 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 product
- Which product is the final product in the reaction below, shown as numbered?Which compounds from 5a-d will react with hydroxide in the fashion shown. Which reaction will be the fastest and slowest? Explain using knowledge of carbonyl chemistry, pka and leaving groups.1. what is the Nature of the leaving group (LG)? 2. what is the relative size of activation energy (Ea) for each reaction? 3. what is the Hammond's postulate? 4. what are the Relative thermodynamic stability of the reactive intermediates? 5. what is Influence of the solvent (if given) on the reactions and intermediates?
- Please help with the following ochem mechanisms.... 1. Provide the stepwise mechanisms for the following reactions (see attached picture)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?Show the SN2 mechanism in the reaction between (S) 2-bromobutane and iodide ion. Label the product and draw a enery diagram for this reaction.
- 1.Draw the product, please shows step by step in details 2.Explain if (CH3)2CH in this reaction can attach in ortho positon in Friedel Craft Alkylation?? why or why not???What major product is expected from the reaction shown in Image 18?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)