осн,сн, HO women HO HO OH wolf Can you help him identify reagent reagent reagent reagent reagent reagent repent reagent Identify the starting alkyne in the following reaction sequence 2 NaNH, CHỊCH8 L NH3(1) NH3( (A) CH3CH2CECCH; (C) CH3CECH 1, Hg(OẠC)2 H2O OH 2 NaBH (B) CH3CH2C=CH (D) CH3CH2CH2CECH OB OD O A
Fenton Reaction HO3 + Felt ki Fe+ + + + HO. Fe+ + H2O, k2Fe+ + OH- + OH HO, + Fel+ + Fe2+ + H OH + Fe+ K OH + Fe+ OH + H2O, SHO, . + H2O HQ Felt H₂O + 6 as the 1st ordor of The reaction rate of fenton reaction with the mechanism as above can be expressed reaction rate as below. - d CH₂02] - K [Fe 3+ ] [H₂O₃] = kobs CH,...
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the review if you guess.
Please explain with detail
Assign the anomeric centres of the following disaccharide. OH OH он O HO OH 2 HO OH 1 OH Select one or more: a. 1-beta O b. 1-alpha O c. 2-alpha d. 2-beta
Assign the anomeric centres of the following disaccharide. OH OH он O HO OH 2 HO OH 1 OH Select one or more: a....
provide the reaction mechanism for this reaction scheme
OH NaBH4 HO o 5% NaOH, 0 °C Vanillin Vanillyl Alcohol
HO HO O H O H H H H H OH OH OH OH OH H OH cs a) Circle the glycosidic bond. b) Identify the type of glycosidic bond that is present in this molecule. c) What type of molecule is this? I- H
4. Write a mechanism that is the reverse of the following reaction: (2 po P o Ho H₂O: a - Photo Prih O=8=0 сон Ó OH o=8=0 H30
Jacobsen's Ligand/Catalyst Mechanism
Can I get help with a detailed mechanism for synthesis of the
Jacobsen's ligand and it's formation of the Jacobsen's catalyst
о он " Y YH 2 equiv K2CO3/Abs EtOH EN NE V HN NH3 Ⓡocco, HO OH reflux, 40 min I C002 reflux, ao min toon hot -OH HO! V Ho- 1. Mn(OA).4H 0 Air, Ethanol, Reflux,-1h 2. LICI, Reflux, 30 min OH HO
i am confused as to how to find the mechanism for this problem
i hope you can help me
OH Br
A possible mechanism for the overall reaction, ОН + NO HNO in the presence of N, is: (HO... NO,) (HO...NO2) OH NO NO2 ОН (HO...NO,) N2 HNO N Apply the steady state approximation to the mechanism, what is the rate of the production of HNO,?
3. Propose a mechanism for the following transformation and answer the following question: A. OH O HO B. Why do you not need to worry about the other hydroxyl group interfering with this transformation?