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- List the given compounds in order of increasing acidity (lowest first). Give a reason for your answer. (picture with i,ii, and iii) A chemist has been asked to make the chemical shown below. Draw and name the oneinitial organic chemical used and devise a synthesis for the chemical below. Ensure you include all reagents and conditions.The product in this reaction is basic enough to be protonated by a dilute HCl solution. Draw the protonated species, clearly showing where protonation occurs. Draw all possible resonance structures of the conjugate acid of the product, and use these to explain why the product is so much more basic than a typical ester, like ethyl acetate.Which of these acid chloride derivatives could you potentially use as a starting material without converting it to another derivative first?
- Please answer this NEATLY, COMPLETELY, and CORRECTLY for an UPVOTE. Arrange the intermediates below in order of increasing basicity:Write the products for (A-I). Label products with the mechanism (Sn2, Sn1, E1, E2) that produced it and write out and label major vs minor elimination products.Can you help answer this problem and elaborate the steps clearly and show any reagent and intermediate steps?
- For the following groups of molecules (labeled A-C), rank the acidity of the molecules in order from least acidic (3) to most acidic (1). Explain your reasoning.A. For the following reaction, give a full curved-arrow pushing mechanism for formation of BOTH products and indicate the Lewis acid and base at each step ( LA or LB ) and whether they are also Bronsted acids and bases (BA or BB). Include all reasonable resonance contributors for any intermediates AND INDICATE THE MAJOR RESONANCE CONTRIBUTOR IF APPROPRIATE B. Indicate which product, A or B, would be formed under thermodynamically controlled conditions and which would be formed under kinetically controlled conditions and give a BRIEF explanation of the role of temperature in determining kinetic and thermodynamic control C. Draw a reaction energy diagram for both reactions on the same diagram.Rank each of the following sets of nitrogen bases in terms of basicity and explain your answer
- Using the retrosynthetic analysis propose a logical route for the following transformation. Draw all substrates, reagents and productsIn the presence of excess base and excess halogen, a methyl ketone is converted to a carboxylate ion. The reaction is known as the haloform reaction because one of the products is haloform (chloroform, bromoform, or iodoform). Before spectroscopy became a routine analytical tool, the haloform reaction served as a test for methyl ketones: the formation of iodoform, a bright yellow compound, signaled that a methyl ketone was present. Why do only methyl ketones form a haloform?In step 2 of the reaction sequence HCl is added to the basic reaction mixture after the reflux period. Show a reaction (with full structures) that explains the purpose of the HCl.