4. Provide the detailed synthetic route to the following target and the retrosynthetic scheme. *NHCHg
4. Provide the detailed synthetic route to the following target and the retrosynthetic scheme. NHCHE m - ir
4. Provide the detailed synthetic route to the following target and the retrosynthetic scheme. pines — is NHCH 5. Provide missing reactants, reagents and conditions in allen - you ya - y - yu-gu
Provide the synthetic route for the following reaction. (4) Provide the synthetic route for the following reaction. C6HsBr C6H3COOH
(4) Provide the synthetic route for the following reaction. C6H5Br C6H5COOH (5) Provide the synthetic route for the following reaction. -CH, -CH2COOH
Provide the synthetic route for the following reaction. (5) Provide the synthetic route for the following reaction. =CH₂ — a -CH,COOH
1. Provide the missing conditions for both steps and show how the amide can be converted to the corresponding acid chloride. Step 1 Step 2 Step 1 Conditions for step 1 (brain-twister: is there just one way?): Conditions for step 2 (same brain-twister): Full reaction scheme: 2. Consider the following reaction: 1. NaOM/MeOH 2. H,0* Does it have a specific name? How many products are possible? Show all of them. Suggest a synthetic route that leads to a lesser number...
6. Provide a synthetic route for the following transformations:
A) at least one retrosynthetic analysis (disconnection) B) a reaction scheme showing each of the synthetic steps with starting materials, products, reagents and conditions C) a paragraph or so describing the logic of a synthetic strategy and why it would be the most likely to give the desired product. octa-2,4,6-triene
17. Provide a synthetic route from benzene to m-bromoethylbenzene aka 1-bromo-3-ethylbenzene. 18. Provide a synthetic route from benzene to p-aminoacetophenone aka 4-aminoacetophenone. 19. Provide a synthetic route from p-methylaniline to m-chlorotoluene 20. Cl KNH2 Liq. NH3 -33 °C
Give a detailed synthetic route to B. using starting material with 3 or fewer carbons. Give a detailed arrow pushing mechanism for each reaction in the route. (12.5pts) Give a detailed synthetic route to A. using starting material with 3 or fewer carbons. Give a detailed arrow pushing mechanism for each reaction in the route. (12.5pts) Give a detailed synthetic route to B. using starting material with 3 or fewer carbons. Give a detailed arrow pushing mechanism for each reaction...