3. Write down the all products for the following reaction. Also write a detail step by step mechanism for the all products formation. 1. CH3MgBr (excess) sos 2. H₂O/H*
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- Give the major organic product(s) for each step of the following reactions (d,e,f)Fill in necessary products reactants or reagants of these reactions. Please note the existence of enantionmers in some cases.For butenafine, develop a synthesis that starts with napthalene and benzene. (aromatic methyl groups can be converted to alkyl bromides using Br2/light, and aldehydes by heating the alkyl bromide in DMSO, eg. ArCH3 to ArCH2Br then to ArCHO).
- please quickly thanks ! 3.Please write out the major reaction and side-reaction in the preparation of ter-butyl.chloride, and write out the key points to use separation funnel in this process.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 productIn light of your answer to Problem 30-40, explain why a mixture of products occurs in the following reaction:
- Find the products for these two reactions. Make sure to include relevant hydrogens, deuteriums and stereohemistry.Hi there, can someone please help me solve for the products of the following reaction? Please make sure to clarify all steps taken to go about solving for the products and explain various terms and rules that should be known or correlate with the question. I'm using these questions to study for our final exam and need some extra clarification on rules and steps. Thank you very much in advance!Study the curved arrows in the reactions below and provide the structures of theproduct(s) formed. One block may represent more than one product/by-product.
- (a) (i) 3-Methyl-2-butanol will react with sulphuric acid to give two isomeric alkenes in 3:1 proportions.(i) Write down the structures for these alkenes and assign appropriate systematic names to them. (ii) Name the most abundant isomer. (iii) Write down detailed mechanism for the formation of a minor product.Chemistry please show detailed mechanisms for the reactions shown below. pleasemake sure to show all work like arrows, charges, and byproducts ect.Which compound is not a possible product in the reaction below ( F2 is in excess F2and UV light the catalyst).CHA + F2 -->O CFAO CHFaO CHF-O CH2F2O CHaF