Principles of Instrumental Analysis
7th Edition
ISBN: 9781305577213
Author: Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher: Cengage Learning
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Chapter 13, Problem 13.21QAP
Interpretation Introduction
Interpretation:
The differences between a monochromator, a spectograph, and a spectrophotometer should be determined.
Concept introduction:
A monochromator is a device that is basically used as a wavelength selector for the monochromatic light incident on it. A spectrograph is a device that separates the wave into all of its incoming wavelengths. Whereas a spectrophotometer is a device that is used to measure the properties like transmittance and the absorbance of the solution.
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4. (2 pts) Draw the structure of the major component of the Limonene isolated. Explain how
you confirmed the structure.
5. (2 pts) Draw the fragment corresponding to the base peak in the Mass spectrum of
Limonene.
6. (1 pts) Predict the 1H NMR spectral data of R-Limonene.
Proton NMR: 5.3 pon multiplet (H Ring
Part VI.
Ca H 10 O is the molecular formula of compound Tom and gives the
in the table below. Give a possible structure for compound Tom.
13C
Signals summarized
C1
C2
C3
C4
C5
C6
C7
13C shift (ppm)
23.5
27.0
33.0
35.8
127
162
205
DEPT-90
+
DEPT-135
+
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2. Using the following data to calculate the value of AvapH o of water at 298K. AvapH o of water at
373K is 40.7 kJ/mol; molar heat capacity of liquid water at constant pressure is 75.2J mol-1 K-1 and
molar heat capacity of water vapor at constant pressure is 33.6 J mol-1 K-1.
Chapter 13 Solutions
Principles of Instrumental Analysis
Ch. 13 - Prob. 13.1QAPCh. 13 - Prob. 13.2QAPCh. 13 - Prob. 13.3QAPCh. 13 - Prob. 13.4QAPCh. 13 - Prob. 13.5QAPCh. 13 - Prob. 13.6QAPCh. 13 - Prob. 13.7QAPCh. 13 - At 580 nm, which is the wavelength of its maximum...Ch. 13 - Prob. 13.9QAPCh. 13 - Zinc(II) and the ligand L form a 1:1 complex that...
Ch. 13 - The equilibrium constant for the conjugate...Ch. 13 - The equilibrium constant for the reaction...Ch. 13 - Prob. 13.13QAPCh. 13 - Prob. 13.14QAPCh. 13 - Prob. 13.15QAPCh. 13 - Prob. 13.16QAPCh. 13 - Prob. 13.17QAPCh. 13 - Prob. 13.18QAPCh. 13 - Prob. 13.19QAPCh. 13 - Prob. 13.20QAPCh. 13 - Prob. 13.21QAPCh. 13 - Prob. 13.22QAPCh. 13 - Prob. 13.23QAPCh. 13 - Prob. 13.24QAPCh. 13 - Prob. 13.25QAPCh. 13 - Prob. 13.26QAPCh. 13 - Prob. 13.27QAP
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- Part VII. Below are the 'HNMR 13 3 C-NMR, COSY 2D- NMR, and HSQC 20-NMR (Similar with HETCOR but axes are reversed) spectra of an organic compound with molecular formula C6H13 O. Assign chemical shift values to the H and c atoms of the compound. Find the structure. Show complete solutions. Predicted 1H NMR Spectrum ли 4.7 4.6 4.5 4.4 4.3 4.2 4.1 4.0 3.9 3.8 3.7 3.6 3.5 3.4 3.3 3.2 3.1 3.0 2.9 2.8 2.7 2.6 2.5 2.4 2.3 2.2 2.1 2.0 1.9 1.8 1.7 1.6 1.5 1.4 1.3 1.2 1.1 1.0 0.9 0.8 f1 (ppm)arrow_forward3. Draw the expanded structural formula, the condensed structural formula, and the skeletal structural formula for 2-pentene. expanded structure: Condensed structure: Skeletal formula: 4. Draw the expanded structural formula, the condensed structural formula, and the skeletal structural formula for 2-methyl-3-heptene. expanded structure: Condensed structure: Skeletal formula: following structurearrow_forwardPart IV. Propose a plausible Structure w/ the following descriptions: a) A 5-carbon hydrocarbon w/ a single peak in its proton decoupled the DEPT-135 Spectrum shows a negative peak C-NMR spectrum where b) what cyclohexane dione isomer gives the largest no. Of 13C NMR signals? c) C5H120 (5-carbon alcohol) w/ most deshielded carbon absent in any of its DEPT Spectivaarrow_forward
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- 8. Choose the compound that will produce the spectrum below and assign the signals to the corresponding protons. 2 4 3 ō (ppm) OH 4 6 6 СОН 2 1 0arrow_forward7. Assign all of the protons on the spectrum below. A B 2 C E 2 1 3 6 4 3 2 1 0arrow_forwarde. If (3R,4R)-3,4-dichloro-2,5-dimethylhexane and (3R,4S)-3,4-dichloro-2,5-dimethylhexane are in a solution at the same concentration, would this solution be expected to rotate plane polarized light (that is, be optically active)? Please provide your reasoning for your answer. [If you read this problem carefully, you will not need to draw out the structures to arrive at your answer...]arrow_forward
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