In first reaction , the first step is formation of imine by attacking with secondary amine. In second step imine is converted to minimum ion , which then react with NaBH3CN and gives final product.
In second reaction first step is diazotisation using NaNO2/HBr. The next step is attack of anisole by removing HBr and final product is obtained.
3. Synthesize the following by showing all the appropriate reagents and intermediates. (6 pts.) b. a....
3. Synthesize the following by showing all the appropriate reagents and intermediates. (6 pts b. CI -NH2 N OCH CI-
3. Synthesize the following by showing all the appropriate reagents and intermediates. (6 pts.) b. CI -NH2 OCH;
3. Synthesize the following by showing all the appropriate reagents and intermediates. (6 pts.) b. CI- -NH2 -OCHE
3. Synthesize the following by showing all the appropriate reagents and intermediates. (6 pts a. N
3. Synthesize the following by showing all the appropriate reagents and intermediates. (6 pts.) COOH CH2NH2 from a. b.
3. Synthesize the following by showing all the appropriate reagents and intermediates. (6 pts.) CH2NH2 from a COOH
3. Synthesize the following by showing all the appropriate reagents and intermediates. (6 pts.) CH2NH2 from a COOH 0-
2. Synthesize the following by showing all the appropriate reagents and intermediates (6 pts.) COOH CHNH from b Connect OFFION
3. Synthesize the following by showing all the appropriate reagents and intermediates. (8 pts.) a. NH осно
2. (6 pts.) Accomplish the following transformation, showing all synthetic intermediates and reagents. en —