We need at least 10 more requests to produce the answer.
0 / 10 have requested this problem solution
The more requests, the faster the answer.
5. (12 pts) How would you prepare the following compounds from the provided starting materials? You...
4.(12 pts) Determine the structure of the compound with a molecular formula of CsH,XO, that is consistent with the data given below. (Hint: Use the provided table to organize your 'H data.) For full credit, be sure to identify "X." MS: M = 184 m/z, M+2 = 186 m/z; peaks have relative intensities of 3:1 IR (cm-1): significant peaks observed at 2920, 1726, 1600, 1480 'H NMR 3 ul 7 6 5 2 PPM Signal Shift (ppm) Integration Multiplicity Identity...
4.(12 pts) Determine the structure of the compound with a molecular formula of C,H,XO2 that is consistent with the data given below. (Hint: Use the provided table to organize your 'H data.) For full credit, be sure to identify “X.” MS: M* = 184 m/z, M+2 = 186 m/z; peaks have relative intensities of 3:1 IR (cm-1): significant peaks observed at 2920, 1726, 1600, 1480 1H NMR 3 9 8 5 4 3 2 PPM Signal Shift (ppm) Integration Multiplicity...
show stepwise how you would prepare the following compounds from the provided starting material and any other organic or inorganic compound. in order to have full credit you mush show all the reactions conditions and the structure of your oroducts in each transformation (30 points) Show stepwise how would you prepare the following compounds from the provided starting material and any other organic or inorganic compound. In order to have full credit you must show all the reaction conditions and...
5. (12 pts) For the molecules below, provide a retrosynthetic analysis to starting materials that satisfy the conditions given. Then give a step-by-step synthetic plan. You may use any reagents you want to accomplish your synthesis. OH O from starting materials containing three or fewer carbon atoms from starting materials containing two or fewer carbon atoms
Q2. Synthesize the following product from the given starting compounds. This will require more than one step. You may use any organic or inorganic reagent to carry out this synthesis. (8 pts each) Do (you can also use any one C reagent) ОН (you can also use any two carbon reagent)
3. Propose reasonable syntheses of each of the following compounds from the given starting materials. You may use any other readily available alkyl halides, solvents and reagents as necessary. More than one step is necessary. Show all intermediates, reactions, reagents and conditions clearly. It is not necessary to show the mechanism. HCECH HCECH , X HCECH HC=CH M H OHC (30 marks)
4. (12 pts) For each of the molecules below, provide a retrosynthetic analysis to starting materials that satisfy the conditions given. Then give a step-by-step synthetic plan. You may use any reagents you want to accomplish your synthesis. HC НОХ H₃C CH весна from propanal as the only carbon source from starting materials containing three or fewer carbon atoms
Show how you would synthesize the following compound starting with acetylene and compounds containing no more than two carbon atoms as organic starting material. You may use any additional reagents you need Br H H Br
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
wing 6 Show how the following compounds could be prepared from the given starting materials. You can use any necessary organic or inorganic reagents. NHCH -NH; CH OH OH ible or an inyersible reaction? Explain.