Fundamentals Of Analytical Chemistry
9th Edition
ISBN: 9781285640686
Author: Skoog
Publisher: Cengage
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
Describe the origin of shot noise in a spectrophotometer. How does the relative
uncertainty vary with concentration if shot noise is the major noise source?
Expert Solution
This question has been solved!
Explore an expertly crafted, step-by-step solution for a thorough understanding of key concepts.
This is a popular solution
Trending nowThis is a popular solution!
Step by stepSolved in 2 steps
Knowledge Booster
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.Similar questions
- A 5.3 × 10-2 M solution is to be used to prepare a series of five 100 mL solutions of varying concentration for use in creating a calibration curve for a spectrophotometric experiment. Determine the concentrations of each of the five dilutions if 10 mL aliquots of the current solution is used for V1.arrow_forwardA molecular exclusion column has a diameter of 7.8 mm and a length of 30 cm. The solid portion of the particles occupies 20% of the volume, the pores occupy 40%, and the volume between particles occupies 40%. (a) At what volume would totally excluded molecules be expected to emerge? (b) At what volume would the smallest molecules be expected? (c) A mixture of polymers of various molecular masses is eluted between 23 and 27 mL. What does this imply about the retention mechanism for these solutes on the column?arrow_forwardIf a molecule fluoresces, what are the advantages of using a fluorimeter instead of a molecular spectrophotometer to detect the fluorophore. How do these instruments differ from one another? How are they the same?arrow_forward
- One method for the quantitative determination of the concentration of constituents in a sample analyzed by gas chromatography is area normalization. Here, complete elution of all the sample constituents is necessary. The area of each peak is then measured and corrected for differences in detector response to the different eluates. This correction involves dividing the area by an empirically determined correction factor. The concentration of the analyte is found from the ratio of its corrected area to the total corrected area of all peaks. For a chromatogram containing three peaks, the relative areas were found to be 16.4, 45.2 and 30.2, in order of increasing retention time. Calculate the percentage of each compound if the relative detector responses were 0.60, 0.78 and 0.88, respectively.arrow_forwardWhen opening the cover of an analytical detector, which optical elements can help us to differentiate whether the instrument is a spectrofluorometer or a UV-Vis spectrophotometer. Justify your answer:arrow_forwardThe response of the instrument must be lincar in the sample matrix. Systematic errors can occur due to sample or standard preparation. It consists of a series of standard analyte solutions separate from the unknown. A blank is used to correct the response from the instrument. Known quantities of a standard solution of the analyte are added to the unknown. It is the method of choice when the matrix of the sample may affect the signal. Matrix effects can cause the same analyte concentration in an unknown and standard to give different responses. It is used to measure the instrument response as a function of a known analyte concentration under a set of conditions.arrow_forward
- 1. From spinach, the chromatographic analysis will yield two major substances: (a) B-carotene (C40H56), which will separate from the spinach mixture to form a yellow band, and (b) chlorophyll A (CSSH72MGN4OS), which will separate from the mixture to form a green band. i. Describe the characteristics and draw structures of these molecules. ii. From the spectrophotometric analysis, what wavelength (Amax) would you expect ß-carotene (C40H56) to absorb? What wavelength would chlorophyll A (CssH72MgN4O5) absorb?arrow_forwardQuantitative Analysis by External Standard Method Calcium in a juice sample is determined by atomic absorption spectrophotometry. A stock solution of calcium is prepared by dissolving 1.834 g of CaCl, 2H20 in water and diluting to 1000.0 mL. A substock calcium solution was prepared by transferring 10.00 mL of the stock to a 100.00 mL volumetric flask and diluting to the mark. Three standard solutions of calcium were prepared by transferring 2.500 mL. 5.00 mL and 10.00 mL of substock to 50.00 mL volumetric flasks and diluting to the mark. The sample is prepared by transferring 1.000 mL of fruit juice from the original bottle to a 25.00 mL flask and diluting to the mark. Strontium chloride is added to all solutions before dilution to avoid phosphate interference. Instrumental response of the standards is measured against the blank, and the following readings are recorded: 9.10, 18.6 and 37.0. The sampie reading is 28.1. Using the multipoint method, find the concentration of calcium in…arrow_forwardFlame Atomic Absorption Spectroscopy (FAAS) method is selected due to its wide applicability for metal ion analysis in drinking water samples. Provide appropriate discussion to determine the concentration of selected heavy metals (Cu and Cr) in the unknown tap water sample.arrow_forward
- 1. State the difference between transmittance, absorbance, molar absorptivity, and fluorescence. Which one(s) is proportional to analyte concentration?arrow_forwardYou have obtained a gas chromatogram of a two component mixture of compounds A and B. The height of peak A is 3.84 cm. and the width at half height is 1 cm. The height of peak B is 3.49 cm. and the width at half height is 1.36 cm. The percentage of a component in the mixture is proportional to peak area. Estimate peak areas by multiplying height by width at half height. What was the percentage of compound B in the mixture? (Enter your answer as a number without any percent symbol or the word percent.)arrow_forwardA standard solution was prepared containing 10.0 ppm of an analyte and 15.0 ppm of an internal standard. Analysis of the sample gave signals for the analyte and internal standard of 0.155 and 0.233 (arbitrary units), respectively. Sufficient internal standard was added to an unknown sample to make it 15.0 ppm in the internal standard. Analysis of the unknown sample yielded signals for the analyte and internal standard of 0.274 and 0.198, respectively. Calculate the concentration of analyte in the unknown sample.arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- Principles of Instrumental AnalysisChemistryISBN:9781305577213Author:Douglas A. Skoog, F. James Holler, Stanley R. CrouchPublisher:Cengage Learning
Principles of Instrumental Analysis
Chemistry
ISBN:9781305577213
Author:Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:Cengage Learning