The following data is for the oxidation of catechol (the substrate) to o-quinone by the enzyme o-diphenyl oxidase. Additional data is also provided for when the reaction is run in the presence of p-hydroxybenzoic acid (PBHA). All data was acquired by monitoring the change in absorbance at 540 nm. Die volgende data is vir die oksidasie van katekol (die substraat) na o-kinoon deur die ensiem o- difenyloksidase. Bykomende data word ook verskaf vir wanneer die reaksie uitgevoer word in die teenwoordigheid van p-hidroksibensoësuur (PBHA). Alle data is verkry deur die verandering in absorpsie by 540 nm te monitor. [catechol] (mM) Rate (AAU/min) Rate (AAU/min) Uninhibited PBHA 1,01 65,02 38,27 0,49 47,11 24,60 0,32 38,44 16,99 0,25 32,84 13,88

The following data is for the oxidation of catechol (the substrate) to o-quinone by the enzyme o-diphenyl oxidase. Additional data is also provided for when the reaction is run in the presence of p-hydroxybenzoic acid (PBHA). All data was acquired by monitoring the change in absorbance at 540 nm. Die volgende data is vir die oksidasie van katekol (die substraat) na o-kinoon deur die ensiem o- difenyloksidase. Bykomende data word ook verskaf vir wanneer die reaksie uitgevoer word in die teenwoordigheid van p-hidroksibensoësuur (PBHA). Alle data is verkry deur die verandering in absorpsie by 540 nm te monitor. [catechol] (mM) Rate (AAU/min) Rate (AAU/min) Uninhibited PBHA 1,01 65,02 38,27 0,49 47,11 24,60 0,32 38,44 16,99 0,25 32,84 13,88

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter20: Dienes, Conjugated Systems, And Pericyclic Reactions

Section20.3: Uv-visible Spectroscopy

Problem 20.5P

See similar textbooks

Similar questions

Carbon monoxide [CO] exhibits an IR absorption at 2143cm-1, acetone [CH3C(O)CH3],exhibits an IR absorption for the CO vibration at 1715 cm-1 and ethanol [CH3CH2OH] exhibits an IR absorption for CO at ~1150 cm-1. Draw Lewis structures of these three molecules and use your structures to explain the observed differences in the CO IR absorption peak frequency (nCO).
10 Wavelength, 1. (nm) E (Red, µ.Mcm- ɛ(Yellow, µMr'cm¬1) Absorbance 500 0.0369 0.000549 0.405 430 0.00506 0.0167 0.474 An orange colored solution is prepared by mixing a red dye solution with a yellow dye solution and the absorbance was measured at the analytical wavelengths of 430 nm and 500 nm. The table provides the molar absorptivity for the red and yellow dye at each analytical wavelength. Calculate the concentration (in u.M) of the red and yellow dye in the mixture. [red] = [yellow] =
One common way to determine phosphorous in urine is to treat the sample after removing the protein with molybdenum (VI) and then reducing the resulting 12-molybdophosphate complex with ascorbic acid to give an intense blue-coloured species called molybdenum blue. The absorbance of molybdenum blue can be measured at 650 nm. A 24-hour urine sample was collected, and the patient produced 1122 mL in 24 hours. A 1.00 mL aliquot of the sample was treated with Mo (VI) and ascorbic acid and diluted to a volume of 50.00 mL A calibration curve was prepared by treating 1.00 mL aliquot of phosphate standard solution in the same manner as the urine sample. The absorbances of the standards and the urine sample were obtained at 650 nm and the following results were obtained. ppm, P aBSORBANCE (A) 1.003.00 0.230 2.00 0.436 3.00 0.638 4.00 0.848 Urine sample 0.518 ffind the slope and intercept, then graph it.
50 uL of an aqueous sample of double-stranded DNA is dissolved in 950uL of water. This diluted solution has a maximal absorbance of 0.326 at 260 nm. What isthe concentration of the original (more concentrated) DNA sample, expressed in ug/ul? I would like to know the process of this question. And I was wondering as well if the total diluted volume would be 950ul + 50ul = 1000ul
You are measuring the concentration of an unknown protein sample, and the absorbance at 595 nm (or A595) of your unknown is greater than that of the highest-concentration standard solution. It is not advisable to simply extrapolate the line of the standard curve to calculate the concentration of the unknown In this scenario, what would be the best strategy to measure the concentration of your unknown (instead of extrapolating from the standard curve)? (answer in 5 sentences)
The biuret reaction is a general method for the determination of proteins or peptides. This method is based on the reaction of the Cu2+ with four NH groups of the peptide bonds, forming a violet complex with an absorption maximum at 540 nm. The intensity of the color is proportional to the number of peptide bonds present, and therefore to the amount of protein. This reaction is specific, the dipeptides and amino acids give a negative reaction, and few substances interfere. A quantity of 19.89 g of fish meat is extracted with 100 mL of glacial acetic acid. Subsequently, 3 mL of the previous solution with 3 mL of the biuret reagent to generate the reaction, after 30 minutes. To reduce errors due to other interfering substances and residual turbidity, the corrected absorbance method Ac is applied to 500 nm and 570 nm. In a study, a standard sample analyzed by the Kjeldahl method (total Nitrogen analysis) is obtained, resulting in 0.43% N (w / v), (Protein content [%] =% N x 6.38). 3 mL of…
A standard of solution was put through appropriate dilutions to give the concentrations of glucose (mM) shown in the accompanying table. The absorbances in the table (1.00-cm cells) were recorded at 490 m table. Use the method of least squares to find an equation relating absorbance and the concentration of glucose.
The students conducted the assay for LDH activity using the two serum samples. Each cuvette (path length 1 cm) contained 3ml of a suitable assay buffer (including pyruvate as substrate). 20 microlitres of either serum was added to the cuvette and the absorbance values immediately recorded at the optimum wavelength for a period of 5 minutes (absorbance readings taken every 30 seconds). Protein concentration of serum sample (mg/ml) Change in absorbance at optimum wavelength per minute Control serum (C) 8 -0.04 Diseased serum (D) 7.8 -0.6 1c. Using the molar absorption coefficient of NADH as 6220 M-1 cm-1, and by application of the Beer-Lambert law, estimate the enzyme activity in the two samples (C and D). Express activity as moles per second. 1d. Estimate the specific activity of the two samples (moles per second per microgram).
There is a class of polyesters that have the general structure shown below. For example, in polyethylene terephthalate (PET) m =1. How would you expect the Tg ad Tm of these polymers to vary with m, given that the molecular weight of the chain is held constant? Give reasons for your answer. Also, assuming that you are now just considering one member of this class of polymers, say PET, how does the Tg vary with molecular weight, n.
7. Suppose you are an employee of a plastics firm and you are assigned the task of identifying a polymer used by a competitor to make certain automotive parts. You prepare a film of the polymer and determine its IR spectrum, as shown below. What information can you deduce from the spectrum? Spectrum below plots transmittance (y-axis) vs. frequency in wavenumber (cm³¹) T прити JU 0 0 0 0 0 1000 3000 2000 1500 1000 500
The functional groups in an organic compound can frequently be deduced from its infrared absorption spectrum. A compound containing no nitrogen exhibits strong, broad absorption across the 2500-3300 cm-1 region, accompanied by 2200 (w) and 1715 (s) cm-1bands.Relative absorption intensity: (s)=strong, (m)=medium, (w)=weak. What functional class(es) does the compound belong to? List only classes for which evidence is given here. Attach no significance to evidence not cited explicitly.Do not over-interpret exact absorption band positions. None of your inferences should depend on small differences like 10 to 20 cm-1. The functional class(es) of this compound is(are)fill in the blank 1.(Enter letters from the table below, in any order, with no spaces or commas.) a. alkane (List only if no other functional class applies.) b. alkene h. amine c. terminal alkyne i. aldehyde or ketone d. internal alkyne j. carboxylic acid e. arene k. ester f. alcohol l. nitrile g. ether
it has been noticed that adulteration of palmoil with carcinogenic dyes is on high.use the knowledge of analytical process to outline protocols you will follow to determine the quantitative and qualitative amount of the toxic dye spectroscopically.