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- Explain why pentane-2,4-dione forms two alkylation products (A and B) when the number ofequivalents of base is increased from one to two.Draw the structure of the organic product formed when the given compounds undergo the three-step reaction sequence indicated. Select Draw Rings More Erase C Br 1. NaOC,H5. C,H5OH 2. NaOH, H2O 3. H3O*, heat1. Identify all products produced in the following reaction. Br MeOH
- Draw out a complete arrow-pushing mechanism for the following reaction. This reaction is explicitly done with heat. O NaOH, H₂O heatComplete the following reaction sequence with the missing major organic products. CH, NaOH CH,CH,CH,CHCH,CHCH,CEN H20 NaOH H,0 CH,CH,The overall dehydration reaction we are performing (the dehydration of cyclohexanol) is reversible and actually slightly endothermic. How can we shift the equilibrium to the product side, assuming we can not limitlessly increase the temperature? Increased magnetic stirring le Chatelier's principle Increased amount of catalyst Extended reaction time
- ОН Type of reaction 1-Propanol is heated Type of reaction H+, Heat IZ + t 1- NaOHDetermine the major product of the reaction shown in the box د b C A B C NaBH CH₂OH Select an answer and submit. For keyboard navigation, use the up/down arrow keys to select an answer. d D OH OH B ON OH C b Dc) Explain why pentane-2,4-dione forms two alkylation products (A and B) when the number of equivalents of base is increased from one to two. i) 1 Equiv. Base i) 2 Equiv. Base ee ii) CH3I ii) CH3I iii) H20 iii) H,O B