13. Which acid in each pair below is the stronger acid? Please explain your answer with the structural considerations presented in class - EWG strength, number of EWGS, or proximity of EWGS. Br Br Explanaation: or н,с EWG strength number of EWGs proximity of EWGS Br он он bromoacetie acid 2-dibromoacetic acid Explanation: сн, снс CH2C EWG strength number of EWGS proximity of EWGS or Он Он 3-fluoropropanoic acid 2-fluoropropanoie seid Choose the more acidic proton from each mo lecule, i.e., each molecule has two acidic protons. which is more acidic? which is more acidic? он но но Он Br Br Why? Why?

13. Which acid in each pair below is the stronger acid? Please explain your answer with the structural considerations presented in class - EWG strength, number of EWGS, or proximity of EWGS. Br Br Explanaation: or н,с EWG strength number of EWGs proximity of EWGS Br он он bromoacetie acid 2-dibromoacetic acid Explanation: сн, снс CH2C EWG strength number of EWGS proximity of EWGS or Он Он 3-fluoropropanoic acid 2-fluoropropanoie seid Choose the more acidic proton from each mo lecule, i.e., each molecule has two acidic protons. which is more acidic? which is more acidic? он но но Он Br Br Why? Why?

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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uestion 10 Which compound shown below is expected to be the least basic, if all are placed in the same solution conditions? (a) (b) CH2CH,NH2 (c) (d) NH N. H. MacBook Pro HIN:
abel basic nitrogens with "B" and nitrogens that are not basic with "X". (f) (h) H (i) H H B (j) (k) H. (1) H. IN H. B. H.
20.)
eq eq M M M ereg 2req 2req 2req X 2req J F3 $ 4 R C V [Review Topics] [References] Draw both resonance structures of the anion formed by the reaction of the most acidic C-H bond of the compound below with base. 4x Include all valence lone pairs in your answer. • For structures having different hydrogens of comparable acidity, assume that the reaction occurs at the less-substituted carbon. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate resonance structures using the symbol from the drop-down menu. ✓✓99.81 O 0- F4 . % 5 T G B F5 *** ^ 6 Cengage Learning Cengage Technical Support Y ChemDoodle H N F6 & N& 7 U O J F7 + [ ] در M 8 PrtScn K F8 9 Home O 83°F Sunny F9 L ) 0 End F10 P Previous C PgUp F11 9 ? Next Save and Exit 9:38 AM 7/18/2022 PgDn F12 0 Ins D Back