Organic Chemistry: Principles and Mechanisms (Second Edition)
2nd Edition
ISBN: 9780393663556
Author: Joel Karty
Publisher: W. W. Norton & Company
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
Chapter 16, Problem 16.10P
Interpretation Introduction
Interpretation:
The operating frequency of an NMR spectrometer using a magnet whose strength is
Concept introduction:
The spectrometer’s operating frequency is the frequency at which a bare proton absorbs radiation when subjected to the spectrometer’s magnetic field.
The gyromagnetic ratio (
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solutionStudents have asked these similar questions
A sample of a red dye and a sample of a blue dye both have the same concentration. Their Absorbance is measured using the same spectrophotometer. At a particular wavelength, will both samples give the same Absorbance reading? Why or why not?
Label below statement as True or False.
When a nucleus is strongly shielded, the effective field is smaller than the applied field and the absorption is shifted upfield .
Problem solving:
• Zinc (II) and the ligand L form a product that absorbs
strongly at 600 nm. As long as the molar concentration
of L exceeds that of zinc (II) by a factor of 5, the
absorbance is dependent only on the cation
concentration. Neither zinc(II) nor L absorbs at 600
nm. A solution that is 1.60 x 104 M in zinc (II) and 1.00
x 103 M in L has an absorbance of 0.464 in a 1.00-cm
cell at 600 nm. Calculate:
The percentage transmittance of this solution
- The percent transmittance of this solution in a 2.50-cm
cell.
- The molar absorptivity of the complex.
Chapter 16 Solutions
Organic Chemistry: Principles and Mechanisms (Second Edition)
Ch. 16 - Prob. 16.1PCh. 16 - Prob. 16.2PCh. 16 - Prob. 16.3PCh. 16 - Prob. 16.4PCh. 16 - Prob. 16.5PCh. 16 - Prob. 16.6PCh. 16 - Prob. 16.7PCh. 16 - Prob. 16.8PCh. 16 - Prob. 16.9PCh. 16 - Prob. 16.10P
Ch. 16 - Prob. 16.11PCh. 16 - Prob. 16.12PCh. 16 - Prob. 16.13PCh. 16 - Prob. 16.14PCh. 16 - Prob. 16.15PCh. 16 - Prob. 16.16PCh. 16 - Prob. 16.17PCh. 16 - Prob. 16.18PCh. 16 - Prob. 16.19PCh. 16 - Prob. 16.20PCh. 16 - Prob. 16.21PCh. 16 - Prob. 16.22PCh. 16 - Prob. 16.23PCh. 16 - Prob. 16.24PCh. 16 - Prob. 16.25PCh. 16 - Prob. 16.26PCh. 16 - Prob. 16.27PCh. 16 - Prob. 16.28PCh. 16 - Prob. 16.29PCh. 16 - Prob. 16.30PCh. 16 - Prob. 16.31PCh. 16 - Prob. 16.32PCh. 16 - Prob. 16.33PCh. 16 - Prob. 16.34PCh. 16 - Prob. 16.35PCh. 16 - Prob. 16.36PCh. 16 - Prob. 16.37PCh. 16 - Prob. 16.38PCh. 16 - Prob. 16.39PCh. 16 - Prob. 16.40PCh. 16 - Prob. 16.41PCh. 16 - Prob. 16.42PCh. 16 - Prob. 16.43PCh. 16 - Prob. 16.44PCh. 16 - Prob. 16.45PCh. 16 - Prob. 16.46PCh. 16 - Prob. 16.47PCh. 16 - Prob. 16.48PCh. 16 - Prob. 16.49PCh. 16 - Prob. 16.50PCh. 16 - Prob. 16.51PCh. 16 - Prob. 16.52PCh. 16 - Prob. 16.53PCh. 16 - Prob. 16.54PCh. 16 - Prob. 16.55PCh. 16 - Prob. 16.56PCh. 16 - Prob. 16.57PCh. 16 - Prob. 16.58PCh. 16 - Prob. 16.59PCh. 16 - Prob. 16.60PCh. 16 - Prob. 16.61PCh. 16 - Prob. 16.62PCh. 16 - Prob. 16.63PCh. 16 - Prob. 16.64PCh. 16 - Prob. 16.65PCh. 16 - Prob. 16.66PCh. 16 - Prob. 16.67PCh. 16 - Prob. 16.68PCh. 16 - Prob. 16.69PCh. 16 - Prob. 16.70PCh. 16 - Prob. 16.71PCh. 16 - Prob. 16.72PCh. 16 - Prob. 16.73PCh. 16 - Prob. 16.74PCh. 16 - Prob. 16.75PCh. 16 - Prob. 16.76PCh. 16 - Prob. 16.77PCh. 16 - Prob. 16.78PCh. 16 - Prob. 16.79PCh. 16 - Prob. 16.80PCh. 16 - Prob. 16.81PCh. 16 - Prob. 16.82PCh. 16 - Prob. 16.83PCh. 16 - Prob. 16.84PCh. 16 - Prob. 16.85PCh. 16 - Prob. 16.86PCh. 16 - Prob. 16.87PCh. 16 - Prob. 16.88PCh. 16 - Prob. 16.89PCh. 16 - Prob. 16.1YTCh. 16 - Prob. 16.2YTCh. 16 - Prob. 16.3YTCh. 16 - Prob. 16.4YTCh. 16 - Prob. 16.5YTCh. 16 - Prob. 16.6YTCh. 16 - Prob. 16.7YTCh. 16 - Prob. 16.8YTCh. 16 - Prob. 16.9YTCh. 16 - Prob. 16.10YTCh. 16 - Prob. 16.11YTCh. 16 - Prob. 16.12YTCh. 16 - Prob. 16.13YTCh. 16 - Prob. 16.14YTCh. 16 - Prob. 16.15YTCh. 16 - Prob. 16.16YTCh. 16 - Prob. 16.17YTCh. 16 - Prob. 16.18YTCh. 16 - Prob. 16.19YTCh. 16 - Prob. 16.20YTCh. 16 - Prob. 16.21YTCh. 16 - Prob. 16.22YTCh. 16 - Prob. 16.23YTCh. 16 - Prob. 16.24YTCh. 16 - Prob. 16.25YTCh. 16 - Prob. 16.26YTCh. 16 - Prob. 16.27YTCh. 16 - Prob. 16.28YTCh. 16 - Prob. 16.29YTCh. 16 - Prob. 16.30YTCh. 16 - Prob. 16.31YTCh. 16 - Prob. 16.32YTCh. 16 - Prob. 16.33YTCh. 16 - Prob. 16.34YT
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
- Two signals appear in the 1H NMR spectrum of thecompound shown here. One has twice the integration ofthe other. The signal with greater area corresponds to achemical shift of 9.3 ppm. The signal with less areacorresponds to a chemical shift of -2.9 ppm. Explain.Hint: Consider the magnetic field lines from a ring currentarrow_forwardTrue or False: The chemical shift of a particular proton provides information about the electronic/chemical environment of that proton. Could you explain how to do this in detail?arrow_forwardNo need explanation please correct answers need onlyarrow_forward
- (True or False): You can determine the identities of substances in a mixture by examining the peaks in an IR spectrum of the mixture. True Falsearrow_forwardCan help me figure out what compounds on from the written on the NMR wave number graph pleasearrow_forwardSolve for the absorbance if only a quarter of the incident light is transmittedarrow_forward
- the shielding in NMR is: a) Place a metal around the sample tube before staining it on the instrument.b) use a metal block to avoid being attacked by an opponentc) blocking the view of a participant in a concertd) when the magnetic moment of an atom blocks the induced magnetic moment of neighboring nucleiarrow_forwardCompute for the linear equation of the following concentration and absorbance given in the table. SAMPLE CONCENTRATION ABSORBANCE 1 0.178 0.2127 2 0.274 0.2715 3 0.473 0.3892 4 0.574 0.4568 5 0.673 0.5327 6 0.864 0.6283 A. y=0.6169x+0.1031 B. y=0.5169x+0.1531 C. y=0.7169x+0.2031 D. y=0.6469x+0.1231arrow_forwardThe absorbance of sample A is higher than the absorbance of sample B. Therefore, sample A has (circle the correct one) more / less dissolved solute than sample B. The absorbance is (circle the correct one) directly / inversely related to the transmittance of a sample.arrow_forward
- Where are Fluorescence spectroscopy is better than Uv-visible spectroscopy? Please shortly answer at your own words. Answer should be to the point.arrow_forwardThe 1H-NMR spectrum of 1-chloropropane shows three signals and the 1H-NMR spectrum of 2-chloropropane shows two signals. Draw these two molecules and determine the relative integrals of each signal.arrow_forwardPlease solve correctly, with some explanation too. (Gpt/ai wrong answer not allowed)arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- Physical ChemistryChemistryISBN:9781133958437Author:Ball, David W. (david Warren), BAER, TomasPublisher:Wadsworth Cengage Learning,Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning
- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning
Physical Chemistry
Chemistry
ISBN:9781133958437
Author:Ball, David W. (david Warren), BAER, Tomas
Publisher:Wadsworth Cengage Learning,
Organic Chemistry: A Guided Inquiry
Chemistry
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Cengage Learning
Organic Chemistry
Chemistry
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:Cengage Learning
NMR Spectroscopy; Author: Professor Dave Explains;https://www.youtube.com/watch?v=SBir5wUS3Bo;License: Standard YouTube License, CC-BY