Explain why benzoic acid is acidic. please explain using inductive and resonance effect as well.
Explain why benzoic acid is acidic. please explain using inductive and resonance effect as well.
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
C. Interestingly, when compared to benzoic acid, p-methoxybenzoic acid is less acidic and m- methoxybenzoic acid is more acidic. Please explain how the location of the methoxy groups influences the pka of each isomer relative to benzoic acid using drawings and a minimum amount of words. TIP: How stable is each conjugate base? What is or isn't stabilizing it? TIP #2: EAS/Aromaticity has nothing to do with it. Meo OME increasing acidity
Hexyne is more acidic than N,N-dipropyl amine. What is the principle effect to explain this? hexyne N.N dipropyl amine A: Element Effect B: Charge Effect C: Resonance Effect D: Hybrid Orbital Effect E: Inductive Effect
Using resonance and induction, explain why sulfuric and nitric acid are such strong acids. Also explain why sulfuric acid is a stronger acid than nitric acid (40 pts).
Please just answer part " b". Please explain your
ranking based on inductive, electronegativity,resonance stability,
size.
4. The following compounds can all behave as bases: NANH2 NaOH CHCH,ОН CH3CH2NH2 NH2 For each compound, draw its conjugate acid. a. b. Rank the acids in order of increasing basicity. Explain your ranking.
Using resonance structures as part of your answer, explain why Br in bromobenzene is: a. A mild ring deactivator b. An o-, p-director. [Note: It is not enough to use resonance structures from part "a" to "prove" part "b". One must show that o-, p-attack is faster, i.e. has lower Ea (AGa) by actually showing an electrophile, e.g. the generalized E+, attacking at the o-, m-& p-positions and, using Hammond's Principle, explain why the o-, p-attacks are favored.] Explain what...
6. Usina resonance structures, explain why acetaldenyde has a pka of 17, while acetone of 19. 7. Using resonance structures, explain why methyl acetate (pka 25) is less acidic than acetone (pka 19). 8. Rank the following in order from least to most acidic. Explain your ranking, using resonance structures with your explanation. & la
You would recrystallize benzoic acid using water as the solvent rather than methanol. Explain why.
Using the elemental, inductive, resonance and hybridizations effects, explain a scenario that would make for a strong Lewis base? i.e. in order to have a strong Lewis base, what kind of structural elements does it need to observe?
why isnt the benzoic acid answer?꙼̈
melting points of Benzoic acid and Phenyl succinate are both
121 celsius in the chart. can you please explain?꙼̈
1. An unknown compound X is one of the four compounds listed in the following table. A mixture of X with benzoic acid melts at 89°C, a mixture of X with phenylsuccinate melts at 20°C, and a mixture of X with m-aminophenol melts at 102°C. What is the identity of X? Explain Chemnical mp. ("C)...