Concept explainers
(a)
Interpretation: The structure of the conjugate acid of monosodium phosphate (base) needs to be determined.
Concept Introduction:Bronsted and Lowry purposed the Bronsted-Lowry acid-base theory. It states that acid can give
(b)
Interpretation: The reason of ineffective use of an aqueous solution of monosodium phosphate for extracting benzoic acid from a diethyl ether solution needs to be explained, if the pKa of conjugate acid of monosodium phosphate is 2.1.
Concept Introduction:Bronsted and Lowry purposed the Bronsted-Lowry acid-base theory. It states that acid can give
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EBK EXPERIMENTAL ORGANIC CHEMISTRY: A M
- (a) Explain how NaBH, in CH;OH can reduce hemiacetal A to 1,4-butanediol (HOCH,CH,CH,CH,OH). (b) What product is formed when A is treated with Ph;P=CHCH,CH(CH),? (c) The drug isotretinoin is formed by reaction of X and Y. What is the structure of isotretinoin? Although isotretinoin (trade name Accutane or Roaccutane) is used for the treatment of severe acne, it is dispensed under strict controls because it also causes birth defects. PPha NaOCH,CH3 HO- isotretinoin HO A Br X Yarrow_forwardCalculate the equilibrium constant for the acid–base reaction between the reactants in each of the following pairs: (a) HCl + H2O (b) CH3COOH + H2O (c) CH3NH2 + H2O (d) CH3N+H3 + H2Oarrow_forwardWhat is the conjugate acid of H2C6H7O5 -1aq2? What is its conjugate base?arrow_forward
- Physiological pH in humans is pH = 7.3. At this pH, would cellular carboxylic acid citric acid (Kal 7.08 x 104) exist primarily as the undissociated free acid or as its dissociated carboxylate form? From the choices provided below, indicate whether the carboxylic acid will exist primarily in its protonated form as a Free Acid or in its deprotonated form as a Carboxylate Anion by clicking on the corresponding button. At equilibrium in this pH, the concentration of the preferred form of the acid is approximately | times higher than the concentration of its conjugate form. Round to the nearest order of magnitude.arrow_forwardPhenylamine is an aromatic amine that is used in the manufacture of dyes. When absorbed through the skin itcauses the Fe+2 in hemoglobin to become oxidized into Fe+3, resulting in the formation of methemoglobin whichcannot bind to or transport oxygen. Phenylamine is soluble in water and acts as a weak base.C6H5NH2 (aq) + H2O (ℓ) ⇋ C6H5NH3+ (aq) + OH- (aq)a. When you measure the concentrations of the ionized substances you find them to be:[C6H5NH2] = 0.234 mol/L [C6H5NH3+] = 2.8 x 10-5 mol/L [OH-]= 2.8 x 10-5 mol/LIf the Kb is 4.27 x 10-10, is the reaction at equilibrium? If not, which direction does it need to move (rightor left) to reach equilibrium? Explain. b. At equilibrium the concentrations of the ionized substances are:[C6H5NH2] = 0.0537 mol/L [C6H5NH3+] = 4.79 x 10-6 mol/L [OH-]= 4.79 x 10-6 mol/LIf this reaction is taking place in a 2.0L container, and 1.5 moles of phenylamine were added to thereaction, what will the new concentrations of the three ionic species be when…arrow_forwardDraw the skeletal structure of the product(s) for the Lewis acid-base reaction.arrow_forward
- Write a net ionic equation to show that piperidine, C5H11N, behaves as a Bronsted-Lowry base in water.arrow_forwardThe pKb of the organic base nicotine (denoted Nic) is 5.98. Write the corresponding protonation reaction, the deprotonation reaction of the conjugate acid, and the value of pKa for nicotine.arrow_forwardThe acid dissociation constant K of trimethylacetic acid (HC(CH³)₂CO₂) is 9.33 × 10¯6. a Calculate the pH of a 3.6M solution of trimethylacetic acid. Round your answer to 1 decimal place. pH = - 0 X Śarrow_forward
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