Answer questions a-c about the Bronsted acid-base reaction below using the identifying letters A-D below each structure. A table of pKa values for various organic and inorganic acids can be found in the references section. A cyclohexanone B benzoate cyclohexanone enolate a) The weaker acid is b) Its conjugate base is c) The species that predominate at equilibrium are (two letters, e.g. AC) D benzoic acid O= OH

To test a spectrophotometer’s accuracy, a solution of 60.06 ppm K2Cr2O7 is prepared and analyzed. This solution has an expected absorbance of 0.641 at 350.0 nm. Several aliquots of the solution produce the following absorbance values.   0.640    0.638    0.640    0.639    0.640    0.639    0.638  is there any significant difference between the experimental mean and the expected value at a 99.9% confidence level?   Question 21 options:   Yes because tcal<tcritical   Yes because tcal>tcritical   No because tcal<tcritical   No because tcal>tcritical

Draw the major organic product of the Bronsted acid-base reaction. Include all lone pairs and charges as appropriate. Ignore any counterions. I :O: NaOH :O: Select to Draw H

[References] Answer questions a-c about the Bronsted acid-base reaction below using the identifying letters A-D below each structure. The pKa's for the acids of interest are: acetic acid (pK, 4.8), and hydrogen bromide (pK,=-9). CH3 Br CH3 H-Br OH B acetic acid bromide acetate hydrogen bromide a) The stronger base is b) Its conjugate acid is c) The species that predominate at equilibrium are (two letters, e.g. ac) Submit Answer Try Another Version 1 item attempt remaining Visited Previous Nex Email Instructor Sav Cengage Learning | Cengage Technical Support

Order the following acids with respect to increasing acidity: I. Fluoroacetic acid      II. Chloroacetic acid III. 3-chloropropanoic acid  IV. Propanoic acid

4) Which direction is favored when dissolved in acetone? Does the answer change if dissolved in methanol? Explain. Nal ce

Organic Chemistry 1 Why did you choose your choice? Explain your reasoning and rational (theory and principles and periodic trends) as to why the species is the strongest base or the strongest conjugate acid. That is to say, provide a reasoning and an answer to your selection/choice. Why did you circle your answer for that particular species?

Please correct these within the same method provided. no stick form i dont like those. i attached the example i dont NOT WANT IT. SO PLEASE DONT USE IT.

Answer questions a-c about the Bronsted acid-base reaction below using the identifying letters A-D below each structure. A table of pka values for various organic and inorganic acids can be found in the references section. ata CH3 CH3 -CH3 CH3 CH,- в D ethoxide ethanol dimethylsulfone anion dimethylsulfone a) The weaker base is b) Its conjugate acid is c) The species that predominate at equilibrium are (two letters, e.g. AC)

3.) Based on the structure of its conjugate base, which acid has the lowest pKa? A. CH3COOH B. CICH2COOH C. BRCH2COOH D. CICH2CHCOOH Keywords: pKa, acid strength, dissociation, conjugate base, elemental effects, inductive-electron withdrawal, hybridization, resonance, electronegativity, proximity Concepts: structural implications for conjugate-base stability