Carry out the synthesis of EACH following products from benzene.
Carry out the synthesis of EACH following products from benzene. NH2 OH Br
30 Design a synthesis of m-bromostyrene from benzene. points Br Part 1 out of 12 Choose the best option for the immediate precursor to the target molecule. Br points НО 23 Design a synthesis of p-t-butylacetophenone from benzene. points Choose the best option for the immediate precursor to the target molecule. Part 2 out of 6 Choose the best option for the precursor to t-butylbenzene. 2 points NH2 OH 23 points NH2 он
9. Provide a stepwise synthesis to carry out the following conversions CN Br Br (a) (b) 2 но,S OH
Aromatic Synthesis Reactions Starting with benzene, propose syntheses to carry out each of the following conversions. Assume ortho and para isomers can be separated.
Design a synthesis of n-propylbenzene from benzene. Hint: A one-step synthesis using CH,CH CH Br and AlBr yields a large amount of isopropylbenzene. 4. 5. Design a high-yield synthesis of each target starting from benzene NO2 NH2 NH2 H2N CI CI target target target target
1. Provide a stepwise synthesis to carry out the following conversion. Br Br 2. Discriminate between the reactants and products by using FTIR 3. Discriminate between the reactants and products by using H-NMR 4. Discriminate between the reactants and products by using C-NMR 5. Discriminate between the reactants and products by using MS Page 1 of 1 1. Provide a stepwise synthesis to carry out the following conversion. Br Br 2. Discriminate between the reactants and products by using FTIR...
Synthesis 18.63) Synthesize each compound from benzene and any other organic or inorganic reagents. Br- CICINO, OYNH2 COOH O2N. -C NH2 НО ОН SO3H HOOC (PABA) sunscreen component
6. Synthesis: (40 pts) Show how you would carry out the following synthesis using inorganic or organic reagents containing four or less carbons. Include the reagents you would need for each step and the structure of the intermediate products formed in each step in the appropriate boxes. A) Cyclobutane 1) 1) 2) Br 0 B) OH 1) 2)
6. Synthesis: (40 pts) Show how you would carry out the following synthesis using inorganic or organic reagents containing four or less carbons. Include the reagents you would need for each step and the structure of the intermediate products formed in each step in the appropriate boxes. Cyclobutane 1) 2) 1) 2) Br B) OH 1) 2)
Synthesize the following compounds from benzene. СООН b Br NO2 NO2 NH2 Br ОН СООН b Br NO2 NO2 NH2 Br ОН
6. Synthesis: (40 pts) Show how you would carry out the following synthesis using inorganic or organic reagents containing four or less carbons. Include the reagents you would need for each step and the structure of the intermediate products formed in each step in the appropriate boxes. CI A) Cyclobutane 1) 2) 1) 2) Br B) OH 1) 2)