ORGANIC CHEMISTRY SMARTWORK5 - ACCESS
2nd Edition
ISBN: 9780393432534
Author: KARTY
Publisher: NORTON
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
Chapter 16, Problem 16.9YT
Interpretation Introduction
Interpretation:
That the integrations of the two signals in Figure
Concept introduction:
The area under an absorption peak is proportional to the number of protons that generate that peak. The higher an integral trace’s stair step rises for a particular signal, the greater the number of protons that contribute to that signal.
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solutionStudents have asked these similar questions
Isoamyl acetate is the primary component of artificial banana flavor. Which signals will be in the positive phase, negative phase, or nonexistent in normal 13C NMR, DEPT-90, and DEPT-135 of isoamyl acetate?
In what ratios would the peaks of an sextet (a signal with six peaks) appear?
Which of the following IR frequencies would be expected for ethanol? Select all that apply.
~1710 cm¹ (broad)
~2870 cm 1
O~2250 cm 1
0-3075 cm ¹
~3410 cm1 (broad)
Chapter 16 Solutions
ORGANIC CHEMISTRY SMARTWORK5 - ACCESS
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
- a The structure of 2 chloroethanol is usually staggered, as shown in this Newman projection: How many distinct 1HNMR signals would you expect from this molecule? Assume that the OH bond is pointing away from the CC bond. b In some circumstances, 2 chloroethanol can be frozen in an eclipsed structure, whose Newman projection looks like this: How many distinct 1HNMR signals would you expect from this molecule?arrow_forwardOnce again, the question is included in the problem. I want to compare it to my answer!arrow_forwardMatch the following functional groups with the associated IR frequency. (all measurements below approximate wavenumbers in cm-¹) Alkene (C-H) Alkane (C-H) Carbonyl (C=O) Alcohol (O-H) 1700 cm^- 3050 cm^-✪ 2900 cm^- 3400 cm^-arrow_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_forwardWhat is the rule for splitting signals?arrow_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
- a. If two signals differ by 1.5 ppm in a 300 MHz spectrometer, by how much do they differ in a 500 MHz spectrometer? b. If two signals differ by 90 Hz in a 300 MHz spectrometer, by how much do they differ in a 500 MHz spectrometer?arrow_forwardExpected number of signals in Styrene 13CNMR how many peaks should be seen between a. 100-150ppm b. 150-220ppmarrow_forwardLabel 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 .arrow_forward
- 2. b) Spectrum 1 and 2 correspond to butanoic acid or ethyl alcohol compounds. Select the spectrum based on respective compound and justify your answer. Spectrum 1 1000 Wavenumbers (em) Spectrum 2 400 500 Wavenumbers (cm) % Transmittance % Transmittancearrow_forwardPlz solve all urgent need. In 30minsarrow_forwardWhat is M+, M+1 and M+2? Label these on spectrum. Calculate number carbons and nitrogen and using the equation. Start by assuming zero nitrogens; if the number of carbons does not come out to be a whole number, use the remainder to justify calculating number of nitrogens. This will not work out perfectly every time! Remember that these will be approximate depending on the signal intensity of the M+ peak and the presence of an [M-1]+ peak that can skew the isotope ratios. If this does not work out, use the value as an approximation to help guide your structure characterization. Calculate the number of oxygens using the equation. If there is no M+2 peak, state this. If the value is too low to be accurate, use it as an indicator for presence/absence of oxygen. This will not work out every time but will be used as a guide to determine chemical formula. Check the nitrogen rule – does it make sense with the M+ you observe and your calculations for N? Check whether fragments…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 LearningPrinciples of Modern ChemistryChemistryISBN:9781305079113Author:David W. Oxtoby, H. Pat Gillis, Laurie J. ButlerPublisher:Cengage Learning
- Principles of Instrumental AnalysisChemistryISBN:9781305577213Author:Douglas A. Skoog, F. James Holler, Stanley R. CrouchPublisher: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
Principles of Modern Chemistry
Chemistry
ISBN:9781305079113
Author:David W. Oxtoby, H. Pat Gillis, Laurie J. Butler
Publisher:Cengage Learning
Principles of Instrumental Analysis
Chemistry
ISBN:9781305577213
Author:Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:Cengage Learning