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- QUESTION 35 Calculate the reaction rate of catalase at room temperature using the following data. Depth of Hydrogen Peroxide Solution Time = 66.3 seconds 2.2 cm O 3.000 68.50 0.080 O 30.140 O 0.033QUESTION 26 Which of these reagents is commonly used to determine the number of polypeptides in a protein? dansyl chloride 2-mercaptoethanol (B-ME) DEAE cyanogen bromide iodoacetate O O O OQUESTION 9 Explain why an Ether (as shown below) has a low boiling but a ketone (propanone) as shown below) has a high boiling point. H;C CH3 H;C CH3 O A. Ether forms weak dispersion forces with itself while Ketone forms strong hydrogen bonds with itself O B. Ether forms weak dispersion forces with itself while Ketone forms strong dipole-dipole interaction with itself OC Ether forms weak dipole-dipole interaction with itself while Ketone forms strong hydrogen bonds with itself O D. Ether forms weak hydrogen bonds with itself while Ketone forms strong dispersion forces with itself. O E. Ether does not form any bonds with itself since there are no H atoms while ketone forms strong hydrogen bonds with itself.
- Question 4 If 32p – labeled (radioactive phosphate) inorganic phosphate were introduced to erythrocytes undergoing glycolysis which of the following molecules would you expect to detect 32 p in Glycolytic intermediates? Select an answer and submit. For keyboard navigation, use the up/down arrow keys to select an answer. a Fructose 1-6 bisphosphate b 3-Phosphoglyceraldehyde Dihydroxyacetone phosphate d 2-Phosphoglycerate e 1-3 bisphosphoglycerate f Phosphoenolpyruvate 3-Phosphoglycerate h Pyruvate i None of the aboveQUESTION 1 Which of the following concepts in column A best fits the concept in column B. p-Nitrophenyl a-D-Glucoside Action of intracellular a-GLUCOSIDASE + NaHCO3 Boiling cells Tris-pH 5.0 A. Substance that act as molecular mimic of a maltose molecule B. Develops TT-Nitrophenyl into a yellow colour reagent for measurement at 400nm c. Breaks the a-linkages of p-Nitrophenyl a-D-Glucoside, leaving p-Nitrophenyl and a glucose molecule D. Allows transport of p-Nitrophenyl a-D-Glucoside across the membrane E. Stop the reaction and release internal p-NitrophenylQuestion 42 The structure below HO, urs O contains trans double bonds O represents an unsaturated fatty acid O does not pack very easily O two of these are correct O three of these are correct O contains cis double bonds O packs easily
- Question 7 Please click here to access the Unit 6 lab experiment video. Please consider the B1 extractions with 1 M aqueous sulfuric acid, which is described in the Unit 6 lab instructions document - Under the acidic extraction conditions with aqueous sulfuric acid, benzaic acid will be found predominantly in what form and in which phase (ether or aqueous)? Benzoic acid is in its protonated form and can predominantly be found in the upper ether phase. O Benzoic acid is in its protonated form and can predominantly be found in the lower aquecus phase. O Benzoic acid is in its deprotonated form las socium benzoate salt) and can predaminantly be found in the upper ether phase. O Benzoic acid is in its deprotonated form (as sodium benzoate salt) and can predominantly be found in the lower aquenus phase.QUESTION 28 Which amino acid is most likely to break an alpha helix? Alanine Isoleucine none of the choices are correct Proline QUESTION 29 If an enzyme has a kcat = 3.3e's-1, Km = 5.9e M, what is its catalytic efficiency? Give your answer in 2 significant figures and scientific notation QUESTION 30 To determine the molecular weight of a purified protein you subject it to ESI mass spectrometry at pH=2. The spectrum i t aiahbeni aln hain m tian Click Save and Submit to save and submit. Click Save All Answers to save all ansuers. 786 Mostly cloudy 9 Type here to searchQuestion 11 Four these are related. Select the exception. amino group O carboxyl group Rgroup (side chain O hydrogen O nitrogenous base
- Question 5 of 40 Side-by-Side Identify the charge states for aspartic acid (Asp), leucine (Leu) and Lysine (Lys) at pH 1, 7 and 12. Then calculate the isoelectric point (pI). Step 7: Determine the appropriate calculation for the pl of lysine. For lysine, the pKa of the amine is 8.95, while the pKa of the carboxylic acid is 2.18 and the pK, of the amine in the Strategy: First identify the sidechain on each amino acid. Then determine whether the side chain is acidic, basic or side chain is 10.53. neutral. Determine whether each functional group is Calculate the pI of lysine. charged or not at the pH indicated. Calculate the (pI) from the pKa values of the functional groups. pI MacBook ProQuestion 16 For a Michaelis Menten reaction the following rate constants were observed: k1 = 7x 107/M-sec k1 =1x 103/sec k2 = 2 x 104/sec The value of Km is: Select an answer and submit. For keyboard navigation, use the up/down arrow keys to select an answer. a 0.3 M b 0.03 M 0.003 M d. 0.0003M e 0.00003 M f 0.000003 M 0.0001 M 0.01 M i 0.001MQuestion 13 Which of the following is the correct structure of the tripeptide Gly-Phe-Ala? a. H-N. Ph H. N. b. HN OH с. H,N. Ph d. OH но Ph NH, O a O b O d * Previous ASSIFICATION OF AMINO ACOS perbes, tis ed on the in chemican VE CLASS CLASSIFI tende nd the LG their co0 useful POLARITY of their R polar, aliphatic R group R group R ter at biological pH, near pH 7.0). ged R group d(basic) Rgroup cidic) Rgroup saov OM HHHIN