4. Consider the following equilibrium: *35*1 Aga Rhaud ng base Bast COR + right. I ress cons. stable OH COO bas wesilir base Strong aa AUX Is the carboxylate anion (CH3CH₂COO) an appropriate base to deprotonate the alcohol? A) yes, because the equilibrium favors the left side AddOH OH B) yes, because the equilibrium favors the right side C) no, because the equilibrium favors the left side P D) no, because the equilibrium favors the right side

4. Consider the following equilibrium: 351 Aga Rhaud ng base Bast COR + right. I ress cons. stable OH COO bas wesilir base Strong aa AUX Is the carboxylate anion (CH3CH₂COO) an appropriate base to deprotonate the alcohol? A) yes, because the equilibrium favors the left side AddOH OH B) yes, because the equilibrium favors the right side C) no, because the equilibrium favors the left side P D) no, because the equilibrium favors the right side

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter10: Alcohols

Section: Chapter Questions

Problem 10.28P: In each equilibrium, label the stronger acid, the stronger base, the weaker acid, and the weaker...

See similar textbooks

Similar questions

In each equilibrium, label the stronger acid, the stronger base, the weaker acid, and the weaker base. Also estimate the position of each equilibrium. (a) CH3CH2O + CH3CCH CH3CH2OH + CH3CC (b) CH3CH2O + HCl CH3CH2OH + Cl (c) CH3COOH + CH3CH2O CH3COO + CH3CH2OH
What is the structure of compound A? 010 Compound A tot 01 Oll O III O IV OV || s ||| Compound A IV COOH
a) Rank the following in order of increasing boiling point. HO CH3 A B b) Rank the following in order of increasing acidity. H3C `OH HS. но. `OH HO A
Which of the following reactions are correct? Explain the answer. + H₂O + H₂O H₂SO4 H OH H OH
What is the best reason why carboxylic acid 3 is the most acidic? aioH cioH а он дон CI- OH OH 1 || F ||| IV A) It is the least sterically hindered. B) The F groups are good leaving groups. C) F is very electronegative and can stabilize a negative charge as FO. D) F is very electronegative and will help to stabilize a negative charge on oxygen via induction. E) The conjugate base is stabilized by resonance.
ОН Type of reaction 1-Propanol is heated Type of reaction H+, Heat IZ + t 1- NaOH
compared to HCO3-, H2co3 has a A Stronger conjugated base B Weaker conjugated base C Higher ka D Lower ka E Both b and c
8 11 12 4: 2 FO F2 W S X #3 Atenolol (Tenormin ™M) HO 80 F3 E D R Ether Ketone Carboxylic acid Ester Alcohol $ 4 C F4 R F % 5 F5 V T G MacBook Air > 6 "NH₂ F6 & 7 H JA F7 * 00 8 B N J DII F8 ( 9 F9 K M -O
Determine the structure(s) of the most favored conjugate base. B) H₂ H3C-C-C=N A) -C=CH
Rank the following 5 alcohols from most acidic to least acidic. -CI COH OH C OH E
What is the major product of the following reaction? OH oc | (1) BH3 (2) H₂O₂, OH-
Which reaction will give butanoic acid? A) B) C) D) Br 1. CH3MgBr Na₂Cr₂O7 2. H₂O NaCN Br Mg all of the above Et₂0 H3O+ heat 1. CO₂ 2. H₂O