3. Two anilinium structures are shown below. Indicate which is more acidic and provide some reasoning...
2) For each of the acids, indicate which proton is more acidic, A or B. Circle the more acidic proton in the structure. Explain your reasoning in one or two sentences (no more!) using a conjugate base stability argument. a. A Fo НО. OH B b. A -H NOH B
Provide a resonance structures which explain why ortho and para nitrophenol are much more acidic than phenol
2-Aminophenol is fairly acidic having a pKa value of ~4.8. Which of the structures shown below (labeled I - IV) is not a valid resonance form of the expected conjugate base. 2-Aminophenol is fairly acidic having a pka value of 4.8. Which of the structures shown below (labeled I - IV) is not a valid resonance form of the expected conjugate base.
Below are two structures known to be acidic at the sites indicated by a dashed arrow. Which of the two is the more acidic? -H H3CH
Predict which proton would be more acidic and explain your reasoning.
Draw 3 resonance structures of SCN. Determine which of the 3 is the most stable. Provide the reasoning for your choice.
5. a) which proton in A is most acidic? Explain thoroughly with resonance structures. b) Decide whether A is more or less acidic than B, and explain your choice.
3. Provide the structures for the products of the reaction shown below? (3 pts) ? HС
3. Provide the structures for the products of the reaction shown below? (3 pts) + HCI
Explain why compound A is more acidic using resonance structures and question 21. WILLUDUlyalli Clemsty ENAM 20. Explain why Compound A is more acidic than Compound B. Use resonance structures to e 21. Which of the following is the least stable carbocation? Circle your response. (2) IV