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- Explain the differences in acidity between p-cyanobenzoic acid and m-cyanobenzoic acid. Illustrate your answer appropriately, showing the acid-base reaction that takes place with each of these and explaining in such terms as electronic (inductive or resonance) and/or steric effects.give clear handwritten solution of all the subparts please!Give a clear handwritten answer..and give all possible products
- Rank the following in order of acidity with 1 being the most acidicCompare the chemical structure of compound A with that of compound B. Answer it in a detailed way. Thank You.aminophylline is a good water soluble derivative of theophylline as ethylene diamine derivative in order to enhance its water solubility for formulation options and to enhance the bioavailability of theophylline . dose complexation phenomena involved in aminophylline preparation? how? show through drawing chemical structure as well as drawing the electronic configuration for complexation
- Identify the correct ranking of the structures from highest acidity to lowest acidity for the bolded hydrogen. The correct answer is D, please explain why that is correct and why other options are wrong.Rank each of the following sets of nitrogen bases in terms of basicity and explain your answerCan you solve all the parts to this question Answer the following questions about the procedure: A. What would be the optical reading of (+/-)-phenylsuccinic acid (racemic phenylsuccinic acid)? B. What would you expect to be the optical reading of pure (+)-phenylsuccinic acid? [Hint: you can find this as a physical property on Sigma.] C. Explain what a reflux is. D. Why can’t you separate (+) and (-) phenylsuccinic acid using a simple recrystallization? E. After the two enantiomers are separated, how can you check the purity of the final solid (how can you determine if it is pure (+)-phenylsuccinic acid)?