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jkn1121

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  1. I just want to make sure, D is True right?
  2. ph3: Structure 2 ph7-8: Structure 2 ph11: Structure 1 A. T since the structure is hydrophic then structure 2 would be capactible B. F since it at ph 11, therefore sturcture is more basic to be capatible C. F, since the structure 2 has the charge to make it acidic
  3. Because it has the charge and it goes with the lower ph since it more acidic
  4. its a neutral structure and its in a chargeless stage but if the unpronated structure is with a pka of 9.2, i think it should be structure 2 instead, right?
  5. Structure 1 is hydrophobic since its neutral and nonpolar can pass through the membrane easily I think the answer is A. F since the pka is very high it wont be soluble in a low ph B. T since the pka will be solube in a hgh ph C. F, ph too low D. T, ph similar close to ph 7,8
  6. 1. Benzylamine is a chemical used as a precursor in the synthesis of some drugs. The amino group in benzylamine has a pKa of 9.3. The other groups in this molecule can be considered not ionizable. Structure 1 The picture above shows the unprotonated form of the benzylamine. Draw the protonated state of this compound. Structure 2 * Suppose to be a NH3 Which structure (or structures) will predominated at the following pHs? (Structure 1 is the original picture (unprotonated) and structure 2 is the one you drew (protonated). pH 3: ______Structure 2____________________________ pH 7 – 8: _____Structure 1__________________________ pH 11: _______________Structure 1__________________ I dont undrstand how this can link into a T/F answerable Based on the structures above (your structure and the original unprotonated structure), which is true about benzylamine? (mark true or false) a. This molecule will be more soluble in water at low pH (for example at pH 3) _____________ b. This molecule will be more soluble in water at high pH (for example at pH 11) _____________ c. If ingested, this molecule is more likely to be absorbed (go through the cellular membrane) in the stomach, at a pH of ~ 1 _____________ d. If ingested, this molecule is more likely to be absorbed in the intestines, at pH ~ 7 or 8 _____________
  7. jkn1121

    Pchem

    If we have 3-Heptanone and 2-Heptanone, what value would we get for 3-Heptanone? Also is the C=O group in the 2-Heptanone structure is replaced by the C=S group or the C=Se group. What dipol moment values would you expect for the resulting structure. I'm not sure how to answer this
  8. Actually that question was kind of off-topic
  9. jkn1121

    pH

    An enzymatic reaction takes place in 10 mL of a solution that has a total citrate concentration of 120 mM and an initial pH of 7.00. During the reaction 0.2 millimoles of acid are produced. a) Using the data in the table below, calculate the final pH of the solution. B) What would be the final pH in the absence of the citrate buffer? Assume that the other components of the solution have no significant buffering capacity and that the solution is initially at pH 7.00. c) What would be the final pH if the solution contained 120 mM of phosphate buffer instead of citrate buffer? Acid Ka (M) pKa ___________________________________ Citric Acid 7.41 x 10-4 3.13 (pK1) Citrate- 1.74 x 10-5 4.76 (pK2) Citrate2- 3.98 x 10-6 5.40 (pK3) H3PO4 7.08 x 10-2 2.15 (pK1) H2PO4- 1.51 x 10-7 6.82 (pK2) HPO42- 4.17 x 10-13 12.38 (pK3) I think using the pH= pka+ log (base/acid) I first take 10m x 120mM= 1200moles, then using 1/2(pka1+pka2) to determine which pka to use ill use pk1 and pk2 and then i get 3.945. Subtract then plug 1200mol for base, 3.945 for pka, and base as .2mM. final ph 7.72?
  10. oh crap i take He g/mol instead of H2, so the answer is 302.21g
  11. I was wondering if the Stronger the Acid, the lower the pka then in a case if a pka=10, then in would most likely be soluble in 0.1M HCl rather than a 0.1M NaOH ?
  12. If P and T cancels out, so R is given and V is 24.8 dm^3, I calculate for n PV= nRT V= nR n= V/R n= 24.8/.0826 = 302.21mol * 4g/mol = 1208g
  13. For A, I said 9-10 since a buffer doesnt change the pH much and when I drew the titration curve the pH range around that area, I guess. I was wondering for D, the relationship between the pH and pka is that when the pH is lower than the pka, the concentration increases since comparing the conc. of NH3, at pH 9, the conc of NH3 is 0.080, then when the pH was 10, the conc. was .028
  14. Ok, so if you are figuring out the volume, M= mol/L ------> L=mol/M L= 0.052/5M NaOH = 0.0104 or is it 0.052/0.1M = 0.52
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