12.54 please provide a synthesis for the following transformations: ( a - „О-О-О-О ОН " - ОН 3 -- Со е зE 3 3 3 3 о: 1ттттт HO
please provide a detailed snswer only use image 1,2, and 3. the partisl image is not an option Which of the following would be most likely to be air oxidized to a quinone? Но NH, НО NH2 НО. НО ОН ( HOM NH2 NH2 NH, но НО он.
Please give a detailed description of the 1H-NMR for fluorescein progide a description of the observed chemical shifts 80 7.25 7.39 7.07 он 0.HO са PPM Please give a detailed description of the 1H-NMR for fluorescein HO PPM
2. (17 points) Consider this alcohol synthesis: ugler, ether ОН a. Provide a clear, stepwise, chemically correct, detailed reaction mechanism for this reaction. obrada to modo non ho mailano
Please provide detailed eplanation. Thanks V. Draw the major productís) of the reactions below. Include all appropriate stereochemistry OH HBr 1) PBr3 2) NaCN он HBr он SoCl2 pyridine 1) HCI 2) NaOMe OH
For the following transformations, please provide detailed conditions to give the designated product in maximum yield with minimum by-products. More than one step may be needed. [8 pts eal a) b) MeO он MeO
Organic Chem 2: please help! 26) Provide a detailed, stepwise synthesis for preparing the molecule on the left below from the molecule on the right and any other reagents necessary Br он
Provide the product of this reaction; please draw a detailed step by step mechanism! Thank you, will give a rating! HO K2CrO tosih H20
Please provide a detailed 13C-NMR analyis please indicate for both the reactant and product the diffrent types of carbon and their peaks. Experiment 10. Synthesis of 3-Nonenoic Acid HO OH heptanal malonic acid Et N reflux 3-noncnoic acid
Please provide a detailed mechanism 8. What is the major organic product obtained from the following reaction? Но но. он H2SO OH OH 2 3 a. 1 b. 2 с. 3 d. 4 ANSWER: b