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- For each of the following reactions predict the major product(s)Complete the following reactions by identifying the majority product(s) or the reaction conditions that are missing. No mechanism is neededThe iodination of acetovanillone (1-(4-hydroxy-3-methoxyphenyl)ethan-1-one) occurs in the following reaction: C9H10O3 + NaI + NaOCl --> C9H10O3I + NaCl Draw the complete reaction mechanism of acetovanillone including curved arrows.
- 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.Predict the major thermodynamic and major kinetic product from the following reaction. Label the major products accordingly. Draw the mechanism (arrow pushing) for each product (2 mechanisms total). Please explain stepsPredict the product with suitable mechanism
- PLEASE SELECT ONLY 1 OPTION FROM THE FOLLOWING ONLY OPTIONS: Elimination 2nd order Radical Halogenation Electrophilic Aromatic Substitution Alkene Addition Substitution Nucleophilic 2nd order Pericyclic Organometallic Coupling React Elimination 1st order OxidationWhich of the following series of reactions is a viable route form the starting material to the product shown below? The correct route is option B but please inlcude a detailed description explaining why and a step by step process:)Predict the major product and the mechanism
- Draw the mechanism for the conversion of propanedial (see Problem 7.43) in its keto form to its enol form under basic and acidic conditions. Do the same for the conversion from the enol form to the keto form.Which of the following reactions occurs more rapidly?!(plz do number 3 , given all possible product , identify major product and give mechanism for each product)