4. Considering the structure of the substrate, the nature of the nucleophile, and the solvent (written...
4. Considering the structure of the substrate, the nature of the nucleophile, and the solvent (written on the arrows), determine the type of mechanism (Snl or S2) for every reaction. Predict the products and draw the mechanism DMF + KN3 ОН + water H-CI а) b) ethanol Br acetone CH3CH20H KI Br d) Br DMSO DMSO Br + КCN KSCH2CH3
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-
2. Predict the product(s) of each of the reaction conditions below. Specify the substrate type (primary, secondary, or tertiary alkyl halide), nucleophile (strong or poor), and the solvent type (protic or aptrotic). Specify the type of reaction mechanism (SN1 or SN2), show the curved arrow mechanism and draw the products as 3D structures to illustrate stereochemistry. Predict the product(s) of each of the reaction conditions below. Specify the substrate type (1º, 2º, or 3 alkyl halide). mucleophile (strong or poor),...
a)indicate the reaction mechanism(s) favored by the particular type of leaving group, substrate, nucleophile/base, and solvent employed; b) predict the major pathway(s) that will occur under these conditions; c) provide the structure(s) of the major product(s) of the reaction ко Ме Me HT H Br Me-N Ме., 'H Me ко Ме Me HT H Br Me-N Ме., 'H Me