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Provide methods for preparing the following through a Grignard synthesis.
a) 3-methylbutanoic acid
b) 2, 4-dinitrophenylacetic acid
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- Provide methods for preparing the following through a Grignard synthesis.i) 3-methylbutanoic acidii) 2, 4-dinitrophenylacetic acidProvide a stepwise synthesis for benzyl alcohol to benzoic acid (including arrow-pushing mechanisms) Steps: benzyl alcohol - sodium benzoate - benzoic acid Kindly show all the arrow pushTo synthesize trans-cinnamic acid from benzaldehyde (PhCHO) and acetic anhydride (Ac2O) under basic, refluxing conditions to exemplify the Perkin condensation. 1. Draw the complete chemical reaction to be carried out. 2. Provide a complete arrow-pushing mechanism for the synthesis of trans-cinnamic acid. 3. Briefly describe the role of water, Na2CO3, and HCl in the isolation of the product. Draw the structure of the product at basic pH (after Na2CO3 addition) and at acidic pH (after HCl addition).
- Prepare the following compound by the synthesis of malonic acidProvide a stepwise synthesis for benzyl chloride to benzoic acid (including arrow-pushing mechanisms) Benzyl Chloride - benzyl alcohol - sodium benzoate - benzoic acid Kindly show all the arrow pushShow how to bring about each step in this synthesis of the herbicide propranil.
- Outline a synthesis of the following compounds (A-C) from acetoacetic ester OR malonic ester. Show the starting material and reagents. If the synthesis is not possible, indicate why. A) hept-6-en-2-one B) 2-benzylheptanoic acid C) 3-isobutyl-2-heptanoneStarting exactly with any acid chloride with exactly with 5 carbon atoms, and using appropriate reagents outline the synthesis of the following molecules: (a) 2,6-dimethyl-4-heptanone (b) 4-propyl-4-octanolProvide a stepwise synthesis for benzyl alcohol to sodium benzoate with reagents KMnO4 and NaOH (including arrow-pushing mechanisms) Please show all the arrow push with the given reagents above.
- Starting with toluene, outline a synthesis of each of the following: (a) o-nitrobenzoic acid (b) m-nitrobenzoic acid (c) 3-chlorobenzoic acid (d) p-bromobenzoic acidPlease don't provide handwriting solution Write a retrosynthetic analysis and synthesis for the following transformation.Illustrate the synthesis of triphenylmethanol via Grignard reactions. Select the appropriate reagents of your choice.