3. Provide the product and a reasonable mechanism for of the reaction below. Note that TSOH (tosic acid) is just a strong protic acid that can be used in polar organic solvents. OH OH 2 cat. H* (from TsOH) product conatins a ketone on a six-membered ring
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- Please help with the following OChem reaction sequence... What is the major product obtained from the following reaction sequence? Also provide the structures for the major organic products formed in each step A, B, C, and D (see attached image)Complete the following reaction. Thank you!Give the major organic product or missing starting material for the following reactions. Please do b or a explain as well.
- Help! Please explain in detail. Thank you! Avobenzone is an active component in many sunscreens. It can exist in an equilibrium between its keto and enol forms. The enol from of avobenzone is given below. (A) Draw the keto form of this compound (B) Which tautomer (keto or enol) exists in a higher equilibrium percentage? Explain your reasoning.ochem help please Predict the major product(s) for the following reaction sequences and provide the stepwise mechanism for both steps 1 and 2 .... (see attached image)final product. b) Draw the correct first step and complete the mechanism, showing the structure of the HO: H. H. НО-Н H. H. .. reaction. H. H a) Explain why the following mechanism is not plausible for the first step of this 2. Consider the following reaction:
- 1. Complete the following reaction and provide the detailed mechanism N' H*6) Complete the following mechanism. (D and SN2) H Br. NaH "H: " 7) Complete the following mechanism. (D and SN2) H NaH "H: " Br. SN2 Good Nucleophile SN2 ether THFPredict the major product of the given reaction and then draw a reasonable mechanism for the product formation using appropriate curved arrow notation. Part 1: OH H2SO4 (aq) view structure Part 2 out of 4 H,0 H,SO4 HSO, HO finish structure . draw structure . H;O*