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- The name for Reaction 1 is _______ Choices: A. Williamson ether synthesis, B. Reduction with Grignard reagent, C. Acidic ether cleavage, D. FC Alkylation The reagent/s for REACTION 1 is/are ______ Choices: A. methanol in acidic medium, B. sodium hydride and bromomethane, C. methyl bromide and aluminum bromide, D. methanoyl bromideUse the appropriate reagent used in the reaction. (d),(e) please!!Synthetize 3-pentynal from 3-butynal using whatever organic/inorganic reagents are needed.
- Propose a short synthesis f or ONE of the following molecules. You can start with acetylene, and alkyl halides from 1-4 carbons in length. You can also use an reagents you wish. a) Hexan-3-one (CH3CH2COCH2CH2CH3)Provide all needed reagents and conditions for each step.Fill in the missing reagents below.
- Give one example of Williamson ether synthesis. Show the reactants materials and the product. Draw the reaction mechanism?rank these from least to most reactive in nucleophilic acyl substitution with a nucleophile I)CH3COOC2H5 II) CH3COO-Na+ III)CH3COCl IV) CH3CONH2Fill in the appropriate reagents for the following reaction:
- select the most appropriate reagent(s) to effect the change. 1. Disiamylborane, 2. HO–, H2O, H2O2 H2, Pd K2Cr2O7, H+ NaOCl H2SO4, HgSO4Show how m-dibromobenzene can be synthesized from benzene from multiple reactions. Tip: think of diazotation as an important reaction in this process.Kinetic and thermodynamic enol products Of 2-butanone conditions? Factors that affect Rate of reaction?...