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 me...
(b) 6pts. Ethyl phenylacetate is a pleasant smelling compound used in perfumery. Show how to convert bromobenzene to ethyl phenyacetate. In addition to bromobenzene, use any other organic and inorganic reagents as necessary. lor polos CH,00,
2. Aklomide, 2-chloro-4-nitrobenzamide, is an ingredient in veterinary antibacterial preparations. Propose a synthesis of aklomide starting with toluene. Show all reagents and all intermediate structures. You do not need to show the mechanism. Assume ortho and para isomers can be separated. NH2 O2N Aklomide
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...
Aromatic Synthesis Reactions Starting with benzene, propose syntheses to carry out each of the following conversions. Assume ortho and para isomers can be separated.
2. Propose a syntheses of the following compound starting with benzene. Assume ortho and para isomers can be separated. (1 UN ONK , COOH COOH
4. Propose an efficient synthesis of the molecule below starting with benzene. You can use any other reagents you want. NOTE: Some reactions produce ortho- and para-products. It is allowable to just take ONE of the products and use it in the next synthesis or claim it as the final product (we assume that ortho- and para-products can be separated). (3 points) CH2CH2CH Br
Starting with Benzene and using any other necessary reagents of your choice a synthesis for the following compound. Assume that ortho and para isomers can be There may be more than one plausible answer.
Starting with benzene and any reagents you need, synthesize compound shown. More than one step is required. Assume you can separate ortho and para-isomers. (12 pts) _CH₂
Using the reagents list below, propose a synthesis of the target compound starting from benzene. Enter your answers as a list of letters corresponding to the selected reagents in order you wish to use them. You may assume that all reactions are appropriately worked up and that mixtures of comstitutional isomers can be separated Remaining Time: 59 minutes, 08 seconds. Question Completion Status: Moving to another question will save this response. Question 1 Using the reagents listed below, propose a...
Using the reagents list below, propose a synthesis of the target compound starting from benzene. Enter your answers as a list of letters corresponding to the selected reagents in the order you wish to use them. You may assume that all reactions are approximately worked up and that mixtures of constitutional isomers can be separated. Remaining Time: 59 minutes, 08 seconds. Question Completion Status: Moving to another question will save this response. Question 1 Using the reagents listed below, propose...