The top half of the image depicts the reaction of the synthesis of N,N-diethyl-m-toluamide (DEET). The...
Propose a stepwise mechanism for the synthesis of N,N-diethyl-m-toluamide (DEET). please show all steps! thanks (CH,CHy), WH -CH,CH) NHCr N(CH, CH,) SOCI -HCI CAM3 -5 CAM
Please analyze the IR and NMR spectra. The product is N,N-diethyl-m-toluamide. The product is obtained by the following reactions Please label all major peaks. Solvent is Et2O. Extracted with NaOH and then HCl and then H2O. Dried and then evaporated. To further purify, hexane was used in column chromatography to elute the product. Then evaporated. CH3 CH3 SOCI2 + SO2 O=0 ОН CH3 CH3 -- + excess (CH3CH2)2NH + (CH3CH2)2NH2* crt ether CI 'N-CH2CH3 CH,CHE 1000 11 100 100 100...
the top half of the image depicts the synthesis of 2-[(3,4-dimethoxyphenyl)methylene]-2,3-dihydro-1H-inden-1-one from 1-indanone and 3,4-dimethoxybenzaldehyde. The bottom half of the image attached shows the table of chemicals used in the reaction. How would I calculate theoretical yield and furthermore, the percent yield? This experiment had a lot of chemicals used and I don't know where to start. Crossed aldol condensation of 3.4-dimethoxybenzaldehyde and l-indanone your co m ments cholateOH -4.0 dehydration formation OH O CHOY carbonyl addition initial aldol product...