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- 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?I need an explanation on the mechanism, linked bellow 1 paragraph explanation on the steps and mechanism. and what the final product is calledSolve 20min I'll give thumbs up! What are the major products for this?
- select the most appropriate reagent(s) to effect the change. 1. Disiamylborane, 2. HO–, H2O, H2O2 H2, Pd K2Cr2O7, H+ NaOCl H2SO4, HgSO4steps and reagents 1. PhMgBr, THF 2. H2O, HCl 3. H2SO4 4. Br2, H2O Please give a detailed mechanismcould you show mechanism and products, and explain the function of the "workup" step? Thanks
- Please show a way to synthesize the reaction Step by step. Thank you! I can use all the practice I can getHi! Are these nucleophiles and electrophiles that I listed int hte image correct? Thanks, ShreyaHi can u help pls as u can see it on the pic i tried to do the mechanism for the formation of dibezyleacetone from acetone and benzaldhyde in a basic condition. I used NaOH . am stuck on benzyleacetone can u continue the mechanism from benzyleacetone to dibenzyleacetone ? I think there are seven or eight steps left thank u