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- Please give me the final product following reaction . Feel free to write out each step! thatd be greatly appreciated!Chemistry please provide the flow of electrons aswell!! thank you! using the starting material (on the left) to determine the sythetic route which will be the most reaosnable and effective to theres none, you have to start witth the begin products to get to finish needed by using the minmium reagents and reactions needed to get to the final productThe reaction below could run through both substitution and elimination reactions. 1. Provide the correct reagent to produce the products shown 2. State which mechanism(s) was followed
- When the following transformation was conducted at an appropriate temperature, the following two products were formed. Provide a mechanism (all steps drawn with complete arrow pushing detail) to account for their formation. Note that n-Bu3SnH is a source of H• and is in excessPredict the major organic product of the following reactions. Please do a,b, c, d or e. Specifically referring to b?Give the major organic product or missing starting material for the following reactions. Please do b or a explain as well.
- I. Of the following reactions, answer what is requested:a) Analyze the type of alkyl halide and determine if the nucleophile is strong or weak and also if it has a basic character.b) According to the previous paragraph, determine if there is competition between the substitution and elimination reactions.c) Describe the mechanism of each of the product (s) that are formedd) Of the product (s) that are formed, indicate which one comes from the substitution reaction and which one from eliminatione) If two or more products are formed, indicate which would be the majority and explain why.Give reactent, products of all reactions subparts below. With appropriate wedge dash when possible.Pls help ASAP, thanks! "Predict the major organic product of the following reaction"
- What is the mechanism for this synthesis? The answer key has two benzene rings but I only get one. How is this possible?Show the mechanism and formation of all products for your alkene for each selected reaction (3 separate complete mechanisms). As part of your submission you must: -An explanation of each step of your reaction (as if you were teaching someone) - Identification of the major product - Explanation for why you selected the major product Please make sure to explain in detail for each of the point listed aboveI don’t get to synthesize this from an ALCOHOL of two carbons or less and benzene. Chloro, in our notes is a ortho/para directing. So I don’t know how you would get a meta substituted benzene