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- 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.NO2 being a deactivating group, increase the acidic nature of alcohol, by increasing the stability of the corresponding conjugate base. True FalseI had written those notes above the nucleophiles, so I am unsure if they are correct.
- Using the information below explain why CN- is a stronger Bronsted base even though in the reaction given it is only 300 fold more nucleopihlic.as a follow-up question can explain this mechanismWithout changing reagent concentrations or amounts, what change could one make to the reaction shown below that would increase its reaction rate explain your reasoning?
- predict the outcome of the reaction of letter C only.The following reaction is one step in the pathway to remove ammonia from the body. Curved arrows are used to illustrate the flow of electrons. Using the starting structure, draw the curved electron-pushing arrows for the reaction. Be sure to account for all bond -breaking and bond making steps. Then draw the missina product of this reaction. Include all lone pairs in the structures. Ignore inorganic byproducts, counterions, Training and solvents.Please provide detailed steps as I am using this to study, along with explanations as to what you did on each step
- Please answer this NEATLY, COMPLETELY, and CORRECTLY for an UPVOTE. Arrange the intermediates below in order of increasing basicity:1.Explain why pyridine ( Kb=2.3x10-9) is a much stronger base than pyrrole (Kb=2.5x10-14), 2.Explain and illustrate, why it is difficult to perfom Friedel-Craft reactions on unactivated pyridine.Complete each Lewis structure, draw all important resonance structures, predict a value for thebond angles requested, and explain your reasoning. a. Nitrous acid (HNO2)HONOHON=ONO= b. Enolate ion (C2H3O) HC1C2=HC2C1=