First Bromination of benzene give bromobenzene followed by friedel craft propylation give desired product.
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4. Propose an efficient synthesis of the molecule below starting with benzene. You can use any...
1. Consider the three molecules below to answer the following questions. Circle TRUE or FALSE at the end of each question (0.5 points each). Molecule A Molecule C Molecule B A. The rate of EAS with Molecule B will be faster than the rate of EAS with Molecule A (assume MAJOR product formation). TRUE or FALSE B. Molecule C will undergo nitration to yield a meta-product that is the MAJOR product. TRUE or FALSE c. The rate of meta-product formation...
1. Propose a synthesis of the molecule below starting with benzene. You can use any other reagents you want. (2 points) сн.CH, но-с-сн, сH;
9. Propose an efficient synthesis of each molecule below starting from benzene and any other reagents needed (organic or inorganic) A. CI B. CI NO2 Br
Ethyl phenylacetate is a pleasant smelling compound used in perfumery. Propose a synthesis starting with benzene. Show all reagents and all intermediate structures. You do not need to show the mechanism. Assume ortho and para isomers can be separated. 3. Ethyl phenylacetate Ethyl phenylacetate is a pleasant smelling compound used in perfumery. Propose a synthesis starting with benzene. Show all reagents and all intermediate structures. You do not need to show the mechanism. Assume ortho and para isomers can be...
3. Propose a synthesis of the molecule below starting with ethylbenzene. You can use any other reagents you want. (2 points) COOH Br
Aromatic Synthesis Reactions Starting with benzene, propose syntheses to carry out each of the following conversions. Assume ortho and para isomers can be separated.
3. Propose a synthesis of the molecule below starting with ethylbenzene. You can use any other reagents you want. (2 points) CH.CH COOH NO2
2. Propose a synthesis of the molecule below starting with toluene. You can use any other reagents you want. (2 points) CH-CH2-O-CH,
Homework extra credit! #18. As promised in lecture... Propose a synthesis of this compound starting with the ind se a synthesis of this compound starting with the indicated material. For full credit you need to write out all the steps, showing the reagents used for each reaction. each step. For reactions that produce both ortho and para isomers, assume that the par e both ortho and para isomers, assume that the para isomer is the major product. This is not...
Propose an efficient and elegant synthesis of the molecule using only a benzene as your starting material. You may use any alkyl halide or alcohol as your other sources of carbon (excluding HCOCl), and any other reagent you deem necessary. OH Cl