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- 1. what reaction and meachanism is this ? 2. Explain mechanism what happenning in each step on this picture 3. why is it says "stop" when NaOEt added ? does reaction stop there ? why does it stop ? ? what principle ?need all 4 parts along with reaction names in detail don't copy or else I will downvotedo not fully undsertand the slide，need further explanation. what does it means by the additive effect of two group？which two group ？？why OH is a more powerful activator than CH3？ meta rarely take please because it is too hindered？why too hindered？Too hindered in EAS or which reaction？why？？I am confused.
- Hello, could someone help me with this practice problem? thx in advance (: For the major product of this reaction, draw the perspective diagram of the major products. The mechanism isn't necessary, just the products. If appropriate, add an enantiomer where required. Lastly, state the stereochemistry of the process (syn, anti or none).For which reaction mechanisms—SN1, SN2, E1, or E2—of thefollowing statement true? A statement may be true for one or moremechanisms. Racemization at a stereogenic center occurs.For the following reactions: A. Draw the missing reactant, reagent or product including the correct stereochemistry where appropriate. B. Determine the Reaction Pathway (Sn1, Sn2, E1, E2) leading to the desired product C. How many steps are in the Reaction as can be plotted on a Reaction Coordinate?
- Show full curly arrow mechanism and talk about regioselectivity/ stereoselectivity. Also define which one is acting as nucleophile, electrophile, base or acid / reaction name. Thank youDraw mechanism for the reactions below. Make sure to show all "electron-pushing" arrows, cond and lone pairs.Hello, could someone help me with these two practice problem? thx in advance (: For the major product of this reaction, draw the perspective diagram of the major products. The mechanism isn't necessary, just the products. If appropriate, add an enantiomer where required. Lastly, state the stereochemistry of the process (syn, anti or none).
- Please solve resynthesis problem with all reagents! Thank you. Training Y1.In retro synthesis: How do we know the bond between Carbon and NO2 will break first?? Why does not Br bond break first? 2. Is it matter that which bond break first ? 3. When it asked "what immediate the precusrsor" , what specificly does it means??? why it's important? 4. What steps or rule should we follow when solving retrosynthesis questions?React molecule with cl2 and identify all mono halogenated products Then label all stereogenic centers, R/S configuration and label reaction products as chiral or achiral Then determine major product using table Lastly draw arrow pushing mechanism to explain formation of major product in halogenation reaction