4. Staring with toluic acid and diethylamine, write an alternative synthesis of the product DEET that does not involve the acid chloride as an intermediate. You may use scifinder in the laboratory to do a reaction search. Provide literature support for your answer.
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- 3. You are given a mixture of aspirin, phenol, and naphthalene that you need to separate. i) Draw the structures of each, and identify if they are acidic, basic, or neutral compounds. For each compound draw their reaction with the appropriate acidic or basic conditions that will change their solubility and allow them to be separated. ii) What modifications would you have to make to the experimental protocol in order to separate these three compounds? Provide specifics.How do you convert Phenol to salicylaldehyde, Name the reaction and Explain with Complete step by step mechanism.?Draw out the reaction (with mechanistic arrows) for the reaction of carbonic acid with water to show the ionization of one proton. Use the editor to format your answer
- C) a nitrile D) an amine nitrite salt DIRECTIONS: Each of the following questions or incomplete statements below is followed by four suggested answers lettered A - D. Select or choose the letters of the best answer to the question or incomplete statement. 7. An organic nitrogen compound, X, gives ammonia on warming with dilute aqueous sodium hydroxide, X could be A) ethanamide B) ethylamine C) phenylamine D) amino ethanoic acid Which one of the following reagents reacts 1. in a similar fashion with both phenylamine (C H,NH,) and ethylamine. A) Br,(aq) C) conc. HNO, D) cold HNO (aq) 2. Phenylamine (aniline) can be prepared by reducing nitrobenzene with tin and concerntrated hydrochloric acid followed by the addition of alkali and finally steam distillation. The alkali is added to; A) prevent oxidation of phenylamine. B) liberate free phenylamine from solution C) dissolve excess nitro benzene D) dissolve the phenylamine 8. Arrange the following molecules in their increasing order of base…20:32 hydroxide 2. Using curved arrows, show the deprotonation mechanism of phenol with (OH). Also, provide the structure of the product of this deprotonation. Start answering this question by drawing the structure of phenol. Then hydroxide ion. Find your most reactive electrons and draw the curved arrow that shows where they would go to deprotonate phenol. Then "make a bond break a bond" write they question 3. Provide valid resonance structures for the product of the previous arrow(s) charge moving onto the ortho- and para positions. Use curved to show how the charge resonates to the next structure in your scheme. all the proper notations for depicting resonance. that show the in the structures Be sure to use Send a chat CTopic: Organic Synthesis Involving Amines: Propose an organic synthesis for 4-bromo-3-nitrophenol. To achieve this, you can use any common reagents of your choosing, and your sole carbon source is 4-bromobenzoic acid. Be sure to describe your process in the discussion text box and also attach a sketch of the stepwise progression of your synthesis process. Hint, this can be done in six major steps shown as reaction arrows. Six major reaction arrows would give one starting material, five intermediates, and one product.
- 4) Write the reaction between cyclohexanecarboxylic acid and thionyl chloride showing all three products (two gaseous and one liquid). Take the liquid product and treat it with 2 moles of dimethylamine in benzene as the solvent. You get two products. What are they? Draw their formulae and write their names.Synthesize Chloramphenicol from Toluene or Benzaldehyde. Draw and explain step by step please.(p.s: if you can, can you write what the reagents does?) (Drug Chemistry)Show how acid derivatives hydrolyze to carboxylic acids under either acidic or basicconditions. Explain why some acid derivatives (amides, for example) require muchstronger conditions for hydrolysis than other derivatives.
- The reaction between propanoic acid and benzyl alcohol in an acidic medium. Show the product by writing the reaction together with its mechanism.1. Create a flowchart for the synthesis and purification of phenacetin. Draw out your steps for the extraction process and label the organic and aqueous layers in your diagrams. Indicate where the product is in each step. 2. Draw the mechanism for the deprotonation of the phenol group of acetaminophen by potassium carbonate. Label the acid, base, conjugate acid and conjugate base. How do you know potassium carbonate is a strong enough base to do this deprotonation?Chemistry Question 2. Compound A is heated with acrolein and base to gives a product as shown below. Provide a detailed step by step reaction mechanism for the formation of the product. H2C= base Compound A Acrolein Need Answer ASAP. Wil Upvote!