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Treatment of but-2-yne with NCS affords an interesting molecule with two methoxy groups and two chloride groups added to it. Please draw a complete reaction mechanism that clearly shows the curvy reaction arrows and explains the product structure.
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- !(plz do number 3 , given all possible product , identify major product and give mechanism for each product)Draw the starting materials and mechanism arrows(s) to give the product shown.Ochem help... What is the major product of the following reaction sequence? Provide the stepwise mechanism for each step (1, 2a, and 2b). (see attached image)
- Please explain, thank you! Treatment of (R)-4-chlorocyclohexene with HCl produces a mixture of four products. Draw the mechanism that accounts for the formation of each product, and identify which products are optically active.Provide the mechanism for each step of the given reaction, showing the major product as well.Based on the mechanism of the reaction, predict the product of the following reactions, and explain your answer with conformation analysis and arrow pushing. Please answer fast I give you upvote.
- How would you synthesize the product from the given reactant in the followingreaction? Show the reaction scheme of each step and draw the mechanismochem 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)Draw a complete stepwise mechanism for the reaction shown below. You must show the structures of all intermediates and indicate electron flow with curly arrows.
- Please provide a detailed mechanism for the following transformation. There are two (2) generally accepted intermediates in this reaction, so only two will be graded. Also, show the appropriate curved arrows to rationalize the next step.Provide the missing reagent(s) needed to complete the following reactions. For each reaction determine whether the mechanism went through a carbocation, a 3-membered ring intermediate, or was concerted. Also indicate whether the reaction follows Markovnikov’s Rule, and is syn or anti addition.Select one activator & ortho para director to be on a benzene ring to start. You will then add a bromine to this group showing the COMPLETE mechanism, including all resonance structures. Put a box around the stabilizing resonance structure and explain why it is stabilizing.