Predict the products of the reaction. In the reaction above, the nucleophile reacts with the carbonyl carbon twice. State which reaction occurs faster, the first addition or the second addition, and explain why. 1) (2 equiv.) 2) H3O+, H₂O MgBr
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- Determine the mechanism of nucleophilic substitution of each reaction and draw the products, including stereochemistr CH₂CH3 CI Br + CN d. + CH3COOH a. acetone + -OCH3 e. DMF f. b. C. ||||| a ||||| Br H Br CH2CH2CH3 + CH3OH DMSO H CH3 CI Br + OCH₂CH3 + CH3CH₂OHFor the reaction sequence below, provide the correct reagents, intermediate or final product. Br You? Na enant.p. please don't provide handwrriten solution Write the mechanism of the reaction with proper arrow formalisim, do not combine into one step
- Write out the expected splitting pattern for hydrogens Ha, Hp and Hc 3Jab = 10 Hz На Hb 3Jpc = 7 Hz CI Hc Hc Ha:Hb:Hc: doublet, quartet, doublet Ha:Hb:Hc: quartet, quartet, triplet Ha:Hb:Hc: doublet, doublet of triplets, doublet Ha:Hb:Hc: doublet, triplet of doublets, doubletCan i see the mechanism for this reactionA student attempted to synthesize an epoxide according to the reaction scheme shown here, but no epoxide was formed. Explain why. Hint: It may be helpful to build a OH NaOH No epoxide model of the reactant molecule. (H3C);C' Br
- What will be the major product of the following reaction and what is the likely mechanism for its formation? (CH;);COK Br racemic OCCCH3)3 OCCH3)3 ÓCCCH3)3 A B C D ERank the following esters from most reactive to least reactive in the first slow step of a nucleophilic acyl substitution reaction (formation of the tetrahedral intermediate): Rank the same esters from most reactive to least reactive in the second slow step of a nucleophilic acyl substitution reaction (collapse of the tetrahedral intermediate).24. Which product is formed by the reaction ? A) | B) || C) ||| D) IV Br ОН NaH Br ... هستم IV