Question

Acetic acid (CH3COOH) and trifluoroacetic acid (CF3COOH) are shown by these particulate models.


Acetic acid (CH3COOH) and trifluoroacetic acid (CF3COOH) are shown by these particulate models. The K, for trifluoroacetic acid is 104times greater than acetic acid. Use the models to account for the differences in magnitude for the K, constant. The yellow atoms are fluorine, the red atoms are oxygen, the black atoms are carbon, and the white atoms are hydrogen.

image.png

 Part 1

Write the formulas for the conjugate bases for the two structures 

The conjugate base of acetic acid

The conjugate base of trifluoroacetic acid


 Part 2 

Which of the following item(s) explain the differences between the Ky values Choose one or more: 

A. The oxidation state for oxygen in trifluoroacetate is more negative than the oxidation state for oxygen in acetate 

B. The trifluoroacetate molecule has more resonance structures than the acetate molecule 

C. The electron-withdrawing fluorine atoms pull electron density from the oxygen in trifluoroacetate. The negative charge is more stabilized in trifluoroacetate by this effect. 

D. The negative charge is on the more electronegative fluorine atom in trifluoroacetate

0 0
Add a comment Improve this question Transcribed image text
Know the answer?
Add Answer to:
Acetic acid (CH3COOH) and trifluoroacetic acid (CF3COOH) are shown by these particulate models.
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for? Ask your own homework help question. Our experts will answer your question WITHIN MINUTES for Free.
Similar Homework Help Questions
  • Acetic acid (CH3COOH) and trifluoroacetic acid (CF3COOH) are shown by these particulate models.

    Acetic acid (CH3COOH) and trifluoroacetic acid (CF3COOH) are shown by these particulate models. The Ka for trifluoroacetic acid is 104 times greater than acetic acid. Use the models to account for the differences in magnitude for the Ka constant. The yellow atoms are fluorine, the red atoms are oxygen, the black atoms are carbon, and the white atoms are hydrogen.Part 1Write the formulas for the conjugate bases for the two structures. The conjugate base of acetic acid  Part 2 Which of the following...

  • Acetic acid (CH:COOH) and trifluoroacetic acid (CF COOH) are shown by these particulate models. The K,...

    Acetic acid (CH:COOH) and trifluoroacetic acid (CF COOH) are shown by these particulate models. The K, for trifluoroacetic acid is 10 times greater than acetic acid. Use the models to account for the differences in magnitude for the K, constant. The yellow atoms are fluorine, the red atoms are oxygen, the black atoms are carbon, and the white atoms are hydrogen. 1st attempt Part 1 (2 points) Write the formulas for the conjugate bases for the two structures. The conjugate...

  • Which of the following statements best explains the decreased acidic nature of carbonic acid compared to...

    Which of the following statements best explains the decreased acidic nature of carbonic acid compared to other carboxylic acids? OH carboxylic acid HO OH carbonic acid A. The extra hydroxyl group on the carbonic acid is an electron donating group, dampening the acidity of the molecule. B. The carbonyl group is an electron withdrawing group, increasing acidity of the OH through resonance. C. The carboxylate anion is stabilized by hyperconjugation and is a weak base, so the conjugate acid is...

  • To compare the acidity of two organic acid, we must the y of their conte bases....

    To compare the acidity of two organic acid, we must the y of their conte bases. The more stable the conjugate base, the stronger the acid. To determine if the conte base is stable, we must follow the below less Negative charges are more stable on trov o LF, Br Larger atoms with negative charge more stable Negative changes preferoide one s than on more electronegative Negative changes to be placed intoms with the more character so they prefers over...

  • Acetonitrile (CH3CN) has a pK, of 25, making it more acidic than many other compounds having...

    Acetonitrile (CH3CN) has a pK, of 25, making it more acidic than many other compounds having only C-H bonds. Draw structures for acetonitrile and its conjugate base using skeletal structures. Use resonance structures to account for the acidity of acetonitrile. draw structure ... Acetonitrile Acetonitrile's conjugate base: draw structure... draw structure ... (negative charge on ) (negative charge on N) The acidity of acetonitrile is accounted for by: O Acetonitrile's conjugate base is stabilized by resonance. O Acetonitrile's conjugate base...

  • Is my understanding of acidity/ basicity correct? Arranging them in order is confusing. In arranging acidity:...

    Is my understanding of acidity/ basicity correct? Arranging them in order is confusing. In arranging acidity: - if the molecules have no charge, consider their conjugate bases: the most stable conjugate base (most stabled negative charge; element effect: high electronegative atom, bigger atom/ inductive effect: the presence of e-withdrawing/ resonance/ hybridization effect: increased %s character) - if the molecules have + charges, conjugate bases are not considered. The most unstable + charged molecule would be the strongest acid. (most unstable...

  • In a covalent bond between two atoms, the more electronegative atom will attract more electron density...

    In a covalent bond between two atoms, the more electronegative atom will attract more electron density toward itself, producing a polar bond. The more electronegative element will carry a partial negative charge, whereas the less electronegative element will carry a partial positive charge. The direction of the bond dipole is always toward the more electronegative element. This is often indicated by an arrow, as shown in the figure. The magnitude of the bond polarity can be estimated by using the...

  • pKa Conjugate base Acid formula Conjugate base name Acid name F3CCOOH 0.20 F3ccoo trifluoroacetic acid trifluoroacetate...

    pKa Conjugate base Acid formula Conjugate base name Acid name F3CCOOH 0.20 F3ccoo trifluoroacetic acid trifluoroacetate ion 13.80 Cl3CCOOH 13.34 0.66 Cl3CCOO trichloroacetic acid trichloroacetate ion HOOCCOOH 1.23 HOOCCOO oxalic acid hydrogen oxalate ion 12.77 Cl2HCCOOH 12.70 dichloroacetic acid 1.30 Cl2HCCOO dichloroacetate ion H2SO3 12.23 1.77 HSO3 sulfurous acid hydrogen sulfite ion 1.92SO42- HSO4 hydrogen sulfate ion sulfate ion 12.08 HCIO2 1.95 CI02 chlorous acid chlorite ion 2.12 H2PO.4 phosphoric acid H3PO dihydrogen phosphate ion 11.88 CIH2CCOOH 2.87 CIH2CCOO 11.13...

  • The reaction is the Pechmann reaction of resorcinol and ethyl acetoacetate to form 4-methylumbelliferone: When HCl...

    The reaction is the Pechmann reaction of resorcinol and ethyl acetoacetate to form 4-methylumbelliferone: When HCl is added to the product, protonation occurs at the carbonyl oxygen of the ester. Draw the conjugate acid of this reaction and explain why 4-methylumbelliferone is more basic than a typical ester. Note: my professor mentioned something about Lewis acids/bases and mentioned how bases are more electron rich. I would like to explain how the product is more basic than a typical ester using...

  • could i see the steps for the questions in each section below , thank you !...

    could i see the steps for the questions in each section below , thank you ! Find the quantum numbers for the following elements | Ca N Te Be2 LI" V U Dy 02 NE TIS Oxidation #s Rules: METALS can have ONLY POSITIVE oxidation #s NONMETALS can have BOTH POSITIVE AND NEGATIVE oxidation #s Find the Oxidation Numbers for the following elements Ag P Li Al Lewis Dot Structure Rules for making your Lewis Dot Structure 1. Calculate the...

ADVERTISEMENT
Free Homework Help App
Download From Google Play
Scan Your Homework
to Get Instant Free Answers
Need Online Homework Help?
Ask a Question
Get Answers For Free
Most questions answered within 3 hours.
ADVERTISEMENT
ADVERTISEMENT
ADVERTISEMENT