Draw the most likely conjugate base resulting from this acid- base reaction. Include all lone pairs. Ignore inorganic byproducts. :0: ü :0: NaOCH2CH3 CH2 0:01 CH2 m
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- Complete the equation for the reaction between each Lewis acid-base pair. In each equation, label which starting material is the Lewis acid and which is the Lewis base; use curved arrows to show the flow of electrons in each reaction. In doing this problem, it is essential that you show valence electrons for all atoms participating in each reaction. (a) (b) (c) (d)b Please help me answer all of this x O Dashboard ở Course: Chem 120 - Organic Che x O LOCAL clicker + A cpp.edu/~Isstarkey/local/clicker/bonding/acid-base.html Arrange the following hydrogens in the order of DECREASING pK, values (from least acidic to most acidic). Arrange the following compounds in order of INČREASING acid strength (from least acidic to most acidic). A)I> II > III -OH HCI CH;OH II III B) III> ||>1 0=C-C-CH2-CF3 OH I C) II > III >I A) III I> II II E) II>I> II C) I < III < II D) II < III < I E) I < II < III Which is the stronger base? Explain briefly. Draw the conjugate acid or conjugate base, as directed, for each. но CH3-C-o conjugate base of NH3 conjugate acid of HO conjugate acid of H:0 hydroxide acetate NH, H20 A) A) Because this is more stable: H-0-H hydroxide is the stronger base. NH. он о B) H20 B) Because this is more stable: H-o hydroxide is the weaker base. NH, OH H2 C) C) Because this is more stable: CH-8-OH acetate is the stronger base. NH, H2 D) D)…What is the expected order of decreasing acidity for the following molecules? Но Но. Но НО I II III IV O III > IV > I > || O1> I| > III > IV O Il > 1 > III > IV Il > | > IV > III O III > IV > I|> I
- CH;COOH +NH; CH;COO+NH, 9. In the above reaction in aqueous solution, the acid reactant is and its conjugate base product is O A. CH3COOH; CH3CO0- О в. СнЗСоон; NH4+ O C. NH3; CH3C00- O D. NH3, NH4+ O E. CH3COOH; H30+c. Explain the trend in acidities: Acid pKa CH2FCOOH CH2CICOOH 2.66 2.86 2.90 CH2BRCOOH CH2ICOOH 3.172. Which is the most acidic hydrogen in the following compound? Provide a brief explanation. H H H. H, II IV +H `H.
- b My Questions | bartleby O Dashboard O Course: Chem 120 - Organic Che X O LOCAL clicker + -> A cpp.edu/~Isstarkey/local/clicker/bonding/acid-base.html What is the most acidic proton in methanol, CHOH Which is the stronger base? Explain briefly. (H, or H,)? Explain briefly (CB = Conjugate Base). NH3 NH2 H-0-C-H H. ammonia aniline A) H, is more acidic. Because carbon is less clectronegative, CB-b is more stable than CB-a. A) Because this is more stable: aniline is the stronger base. -NH2 B) H, is more acidic. Because carbon is less electronegative, H, is more stable than Hp- B) Because this is more stable: ammonia is the stronger base. -NH2 C) H, is more acidie. Because oxygen is more electronegative, CB-a is more stable than CB-b. C) Because this is more stable: NH3 aniline is the stronger base. D) H, is more acidic. Because oxygen is more electronegative, H, is more stable than Hp. D) Because this is more stable: NH2 ammonia is the stronger base. E) H, is more acidic. Because oxygen…1. Identify the acids and bases in the following reactions: (a) CH3OH + H+ CH3OH2+ (b) СН3ОН + NН2 CH30- + NH3 (c) ZnCl2 || || + ZnCl2 H3C° H. H3C H.Select (highlight) the most acidic atom of the compound, and um topic H₂C OH
- For each group of anions, rank in order of increasing conjugate base strength. Briefly explain. яroup 1 group 2 :0: Cl- Br- BrThe hydride ion is very basic and reacts readily with compounds having even weakly acidic protons to form H2. True or false?Draw the most likely conjugate base resulting from this acid-base reaction. Include all lone pairs. Ignore inorganic byproducts.