a) Draw mechanism/product for aldol reaction: NaOet ethanol (solvent) c) Final product if result is protonated with mild acid in an ice bath. d) Final product(s) it result is Awarmed) with excess H₃O+
Explain the effect of the solvent on the reaction kinetics with respect to an SN1 mechanism? - solvent used was 60/40 acetone/water solution up to 100ml
SN2 stepwise mechanism with arrows, the substrate and solvent effect on the reaction, and the stereochemical and regiochemical outcome for the reaction
HCI Choose the correct mechanism and then the solvent that is best for the reaction. CH3OH X Сн,он OCH DMSO SN2, DMSO SN1, DMSO SN2, CH3OH Sn1, CH3OH
in the solvent-free synthesis of chalcones, Discuss the key aspects of the mechanism and why the equilibrium favors product. + OCH3 OCH3 OCH3 OCH3 e come OCH3 OCH3
show complete mechanism including if steps are reversible or not OH cat. KOH H2O (solvent)
Draw a FULL reaction mechanism for the formation: reactants: sodium saccharin with iodoethane in the solvent DMF a) N-ethylsaccharin b) O-ethylsaccharin
provide a stepwise mechanism: 10. Provide a STEPWISE Mechanism for the following 40pts a) excess CH3l NH H2CCH2 Ag2O H20, Heat
Determine, based on the identity of the substrate, nucleophile, and solvent, the mechanism of nucleophilic substitution of each reaction and draw the products, including stereochemistry. OTS DMF y uns + ⓇCN MeCN 3) M Br + H3C-0-
what would the mechanism be for these NH2 NaB (CN) Hz CH,OH solvent OCH3 Reductive I-2 NaB (CN) HZ H2N CH,OH solvent