1. Predict Product: H 2. Propose a synthesis of the polystyrene using the carbon-containing compounds (shown...
Please propose a synthesis of the following compounds from the given starting materials. You may use any other reagents and/or additional carbon containing compounds you wish. Multiple steps may be required. OO O I H^CH3 NO2 N
Provide a step-wise synthesis of the molecule shown below using the two starting materials provided and anything else you may need. 5. Provide a stepwise synthesis of the molecule shown below using the two starting materials provided and anything else you may need. a. anything plus any other molecule containing 1 C plus any other reagents necessary. cl Hint: this is a highly convergent synthesis. You will need to prepare two separate molecules, then birng them together to form the...
1) Propose a synthesis of the following amine from ethanol. Ethanol should be the only carbon source you use. 2) Propose a synthesis. 3) Propose a synthesis. 1) PCC pn. 3)acid work up 5) 03 6) DMS 7)? 8)? 9) H/Ni 4) Propose a synthesis. 5) Name the following using IUPAC nomenclature.
Question 3 Propose a stepwise synthesis for N-propylbutanamide, using 1-propanol and/or carbon dioxide as your only source of carbon and any other reagents necessary. Testbank, Question 140a Using the reagents below, list in order (by letter, no period) those necessary to provide this synthesis Note: Not all spaces provided may be needed. Hints: First receive a Grignard reagent in steps 1 and 2. Use propanol in step 5. In step 9 a product from step 4 reacts with a product...
Propose a stepwise synthesis for N-propylbutanamide. using 1-proanol and/or carbon dioxide as your only source of carbon and using any other reagents necessary. Detail how the final product could be identified using a spectroscopic method.
H H-N 1) What is the overall charge of the above compound when placed in an aqueous pH 7 buffer? A. O, zero B. +1 C. +2 D. +3 or +4 2) Predict the resulting product from the following multi-step synthesis shown below: O NaoMe NaoMe MeOH / dil HCI H30+ Δ Ph2P=CH2 ОMe ? Br Br NaOME O OH OH P+Ph3 Br A. Br D. B. CO2H
reaction mech: initiation , propagation, and termination of the synthesis of polystyrene Polymersti 2. Write the reaction mechanism (showing arrows) of the synthesis of polystyrene. 4pts • Include and show arrows in 2 initiation steps with benzoyl peroxide forming the phenyl radical. (this is shown in Figure 9 of the lab- just add all arrows) A propagation step of the styrene (the monomer) and phenyl radical. A second propagation step showing polymer growth by reacting styrene and the radical product...
1) Propose a synthesis of the following amine from ethanol. Ethanol should be the only carbon source you use. Lfcce HN 2) Propose a synthesis. OH 3) Propose a synthesis. Ph OH 1) PCC 2) 3)acid work up 4)2 NH 5) O3, 6) DMS 7)? 8)? 9) H2/Ni 4) Propose a synthesis. HN 5) Name the following using IUPAC nomenclature. Br
4-2 Indicate whether or not each of the following four- carbon oxygen-containing compounds has a carbonyl group present in its structure. a. CH3-CH2-0-CH2-CH3 b. CH3-CH2-C-CH3 C. CH3-CH2-CH-CH2-OH od. CH3-CH2-CH2-C-H
Design an effective synthesis for each of the following amino acids starting from the compounds shown on the left. You may also use any monofunctional organic compound containing four or less carbon atoms, and any inorganic reagents in your syntheses.