a. 3. For the following IUPAC names, draw the corresponding structure. Include correct stereochemistry where necessary. (2E)-penta-2,4-dienoic acid
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- Can you assit with confirming product(s), define major/minor, show stereochemistry, if appropriate, and/or if no reaction occursArrange the structure on the image with regard to the reactivity towards hydrolysis. 1 being the least and 3 being the mostFill in the missing reactants, reagents and products in the following reactions. Indicate stereochemistry if necessary. Unless otherwise specified, assume the reagents are in excess. PLease explaion with MUCH detail.
- Predict-the-product. Draw the structure(s) of the major organic profuct(s) formed in the following reactions. Please indicate stereochemistry if appropriate.Provide the E2 mechanism for β-elimination reactionemploying 2-chloro-2-methylbutane to prepare 2-methyl-2-butene and 2-methyl-1-butene reaction. Use the actual structures of thereactants and products. Explain which of the alkenes is the major product ofthis reaction ?(A) Provide the major organic product for the reaction below (B) Would the product be optically active of optically in active?
- Hydrogenation of alkene A with D2 in the presence of Pd-C affords a single product B. Keeping this result in mind, what compound is formed whenA is treated with each reagent: (a) mCPBA; (b) Br2, H2O followed by base? Explain these results.Identify the pericyclic reactions in the followingreaction schemes. Give the complete reaction name and indicate the course of the reaction with the aid of the arrow notation.APPLY STEREOCHEMISTRY WHEN APPLICABLE: Does each reaction occur from SN1 or 2? What are the organic products?
- Synthesis: need to provide the likely organic products, keeping in mind regiospecificity and stereochemistryUsing the attached molecule and synthesis, please redraw the molecule showing the stereochemistry attained through the synthesis.give the major products and include stereochemistry when appropriate