Ring opening of unsymmetrical epoxide by SN2 manner and occurs at least substitited side.
Hence A is major
Please help with mechanism. (please draw all curvy arrows charges and electrons. Explain using mechanism which...
Could you help me write a detailed mechanism for the following problems? All arrows, charges, and electrons must be included. In addition, could you help decipher which would be the major/minor product while providing an explanation? laase write the detailed mechanism for the following reaction. Please draw ALL CURVY DOWS charges and electrons. Explain using mechanism which will be major product A or B.( pts) BIZ mub -OX HO Brand B ps) Он Но, NaH НО.
please help. thanks Q4. Please write the detailed mechanism for the following reaction. Please draw ALL CURVY ARROWS charges and electrons. Explain using mechanism which will be major product A or B. (9 pts) Hount . Et and X
How to do synthesis of both? Explain and draw all electrons and arrows and charges please, with all reagents. A) 3Y A) 3Y
The second picture is the actual starting material, it has an extra carbon after the OH. Q5. Please write the detailed mechanism for the following reaction. Please draw ALL CURVY ARROWS charges and electrons. Explain using mechanism which will be major product A or B. (9 pts) OH HO NaH HO HC OH3
2. Draw all the resonance forms for the following compounds. Use curvy arrows to show the flow of electrons. (8 pts)
Please draw the curvy arrows of this mechanism. 1. BH THF 2. ILO.OH он 3,3-dimethyl-1-butene 3.3-dimethyl-1-butanol +3.3-dimethyl-2-butanol?
Please help with this mechanism Draw the mechanism for the reaction of an alkyl halide with sodium azide, followed by reduction. Follow the directions on each step. Complete the mechanism of the initial step of the reaction of the alkyl halide with sodium Complete the product structure by adding any missing atoms, bonds, charges, and nonbonding electrons. Omit curved arrows. Predict the organic product of the LAH reduction and hydrolysis steps; include nonbonding electrons. Do not include any inorganic products.
Using arrows to designate the flow of electrons, predict the major product(s) and the mechanism of the reaction below. provide all possible product(s), hand draw the response on a piece of paper. No cutting and pasting from the Internet, You can only upload an image of your response, Initial your name next to each response. С 80 oC Xylene
#1. Using curved arrows to symbolize electrons, write a complete reaction mechanism for the bromination of acetanilide to create the product. Include the resonance structures for any charged, delocalized intermediates that are involved. #2. Why does performing the experiment at 0 degrees Celsius help you identify some of the relative rates of reactivity? #3. Explain why a methyl group is a mildly activating group while a methoxy group is strong activating. #4. Explain why-- NH2 act as an activator and--...
2. Elimination - draw the mechanism arrows that explain the electrons that changed for the formation of the alkene product E2 - 2 molecules collide Hocas + k'ko bistan woman on ollut 3. List above molecules from best to worst Nu: 4. Best to worst leaving group?