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NOTE: Third option is incorrect answer
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- 1. Which of the following compounds is most acidic? a. I b. Il с. ||| d. IV e. V I ОН II ОН Br III ОН Br Br IV ОН V F ОНRank the bold-faced hydrogens for the following compounds from most acidic to least acidic. H I O A. II > IV> ||| >V>I OB. II > IV> V> ||| > I OC. IV>II> I > V > III O D.V> III > IV> || > | OE. IV>II> ||| > V > I II CI CO₂H CKH Н III W n IV CO₂H2A. Rank the following compounds with increasing acidity: (1 = least acidic; 3 = most acidic) Me Me Mo Me (c) Se H. (d) H. .H H.
- Highest acidity Lowest acidity Answer Bank H;C. CH -CH, CH3 H3C H. H H H. 从山 H- -0-CH3 H3C CH3 H.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+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…
- For the molecule with formela GH,ON please draw the Congtitutional isomers withthe properties as ndicated below ALL the cansttutanl isomera molecule of 'this aromatic ring contain Draw Gingle (R) 9tere agenic center any Congttutional isomer with a BO) Draw heteroatom CN oro) in the aromatie ring a congtitutional iscmer that has for the molecule you Show the mogt acidic proton drew in Boxi by drawing the conjuga te base e Draw a Conot tutonal isomer where the mogt acidic proton hao a pka of-5 Draw a congtitutional isomer with aldehyde functional goue dreus in vi) for the molecul you Show the most acidec pro ton by duawing Show the most acid veus In Box y the Conjugate base Oraw a congttutional igomer trat eantain an ester tunctional graffPart A Arrange the following solutions in order of increasing basicity: Rank solutions from least basicity to greatest basicity. To rank items as equivalent, overlap them. Reset Help KOH KCHO2 C;H;NHNO, KBr (C,H;);NHB. Least basicity Greatest basicityTWO POSSIBLE TAKE PLACE PROTON TRANSFER REACTIONS cAN BETWEEN THE FOLLOWINn REACTANTSS. 0-H a. WRITE THE PRODUCTS OF EACH POSSIBLE PROTON TRAWS FER REACTION. iS MORE FAVORABL WHI CH REACTION REASONINA. 6. DETERMINE EXPLAIN YOUR
- HELPP MEEE i need the answer of this please, if you can help me, please doitArrange the following species as most stable in solution to least stable in solution using the K, of their conjugate acids. C6 H;O Ka • ClO, Cio- 1.6 x 10-10 Ka = 1.2 x 10-2 Ka = 3.5 x 10-8 Ka = 1.0 x 10-48 CH5 Most Stable lons 1 | Cio- | CiO, 3. CH3 C6 H5O .... 2. 4.:The degree of dissociation of a weak acid HA is given as 1.82 %. It can also be stated as 0.00182 (dimensionless). .a O 0.0182 moles. .b O 0.00182 moles. .c O 0.0182 (dimensionless). .d O