Identify the MAJOR product(s) that would be obtained from the following TWO-STEP reaction sequence. 1) Br2 (1 equiv) 2) Cl2 Nal (excess) CI Br (+ enantiomer) Br Br Br Br CI
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- Please label all the steps and reagents with their corresponding letter. Thanks!Please show the major products with stereochemistry where needed.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 product
- The product of reaction between acetone and bromine (excess) with KOH excess is A. Ch2BrCOCh3 B. ChBr3 C.ChBr2COCH3 D.CBr3COCH3 E.Ch2BrCOCHBr2Why 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 configuration1. 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)Please draw the mechanism (assuming an SN1pathway) for the reaction of cyclopentyl bromide with the cyanide anion (-CN) to yield cyclopentyl cyanide as the organic product Thank youPlease assign the missing products or reagents (A till E) in this scheme.
- What major product is expected from the reaction shown in Image 18?Supply the missing reagent in the following reaction: (see attachment) A. Lindlar, H2, mCPBA B. O3 or KMnO4 C. fused KOH D. NH3 E. NaNH2Attached compounds undergoes E2 elimination with strongbase? For compounds that undergo elimination, draw the product. Forcompounds that do not undergo elimination, explain why they are unreactive.