Foundations of College Chemistry, Binder Ready Version
Foundations of College Chemistry, Binder Ready Version
15th Edition
ISBN: 9781119083900
Author: Morris Hein, Susan Arena, Cary Willard
Publisher: WILEY
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Chapter 15, Problem 72AE
Interpretation Introduction

Interpretation:

Volume of 12.1 M HCl required to be added to 3 L of 3.25 M HCl so as to prepare Ehrlich reagent has to be calculated.

Concept Introduction:

The acidity strength is quantified by the magnitude of a parameter called pH. The strong acids tend to lower values of pH. This is since pH represents the negative logarithm of the concentration of H+ ion. So higher the concentration of H+ ion lower will be pH.

The expression to evaluate pH is as follows:

  pH=log[H+]

Here,

[H+] denotes concentration of H+ ions.

The dilution formula is given as follows:

  M1V1=M2V2

Here,

M1 denotes molarity of  initial solution before dilution.

V1 denotes the volume before dilution.

M2 denotes molarity of final solution after dilution.

V2 denotes volume after dilution.

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2. Predict the NMR spectra for each of these two compounds by listing, in the NMR tables below, the chemical shift, the splitting, and the number of hydrogens associated with each predicted peak. Sort the peaks from largest chemical shift to lowest. **Not all slots must be filled** Peak Chemical Shift (d) 5.7 1 Multiplicity multiplate .......... 5.04 double of doublet 2 4.98 double of doublet 3 4.05 doublet of quartet 4 5 LO 3.80 quartet 1.3 doublet 6 Peak Chemical Shift (d) Multiplicity
Interpreting NMR spectra is a skill that often requires some amount of practice, which, in turn, necessitates access to a collection of NMR spectra. Beyond Labz Organic Synthesis and Organic Qualitative Analysis have spectral libraries containing over 700 1H NMR spectra. In this assignment, you will take advantage of this by first predicting the NMR spectra for two closely related compounds and then checking your predictions by looking up the actual spectra in the spectra library. After completing this assignment, you may wish to select other compounds for additional practice. 1. Write the IUPAC names for the following two structures: Question 2 Question 3 2. Predict the NMR spectra for each of these two compounds by listing, in the NMR tables below, the chemical shift, the splitting, and the number of hydrogens associated with each predicted peak. Sort the peaks from largest chemical shift to lowest. **Not all slots must be filled**
11:14 ... worksheets.beyondlabz.com 3. To check your predictions, click this link for Interpreting NMR Spectra 1. You will see a list of all the - compounds in the spectra library in alphabetical order by IUPAC name. Hovering over a name in the list will show the structure on the chalkboard. The four buttons on the top of the Spectra tab in the tray are used to select the different spectroscopic techniques for the selected compound. Make sure the NMR button has been selected. 4. Scroll through the list of names to find the names for the two compounds you have been given and click on the name to display the NMR spectrum for each. In the NMR tables below, list the chemical shift, the splitting, and the number of hydrogens associated with each peak for each compound. Compare your answers to your predictions. **Not all slots must be filled** Peak Chemical Shift (d) Multiplicity 1 2 3 4 5

Chapter 15 Solutions

Foundations of College Chemistry, Binder Ready Version

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Solutions: Crash Course Chemistry #27; Author: Crash Course;https://www.youtube.com/watch?v=9h2f1Bjr0p4;License: Standard YouTube License, CC-BY