PREPARING F/YOUR ACS EXAM IN GEN CHEM
PREPARING F/YOUR ACS EXAM IN GEN CHEM
18th Edition
ISBN: 9781732776401
Author: EUBANKS
Publisher: American Chemical Society
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Chapter ER, Problem 13PQ
Interpretation Introduction

Interpretation:

The reaction, which occurs when iron and zinc metals are to the solutions containing Fe2+,Zn2+ ions has to be predicted.

Concept Introduction:

Standard reduction potential:

The standard reduction potential is in a category known as the standard cell potentials or standard electrode potentials.  The standard cell potential is the potential difference between the cathode and anode.  The standard potentials are all measured at 298 K , 1atm  and with 1 M solution.

The relation between the reduction and oxidation potential is,

  Eoreduction=-Eooxidation

Expert Solution & Answer
Check Mark

Answer to Problem 13PQ

Zinc metal will reduce Fe2+ ions.  Hence, option (D) is correct.

Explanation of Solution

Reason for the correct answer:

Considering the choice (D) the overall reaction is,

  Zn(s)Zn2++2e(aq)+0.76VFe2+(aq)+2eFe(s)-0.44V___________________________________Fe2+(aq)+Zn(s)Fe(s)+Zn2+(aq)+0.32V

The overall standard electrode potential is +0.32V this positive cell potential value is associated with the spontaneous reaction.  Thus, option D is correct.

Reason for incorrect answer:

The overall reaction for option (A) is ,

  Fe(s)Fe2+(aq)+2e+0.44VZn2+(aq)+2eZn(s)0.76V___________________________________Fe(S)+Zn2+(aq)Fe2+(aq)+Zn(s)0.32V

The overall standard electrode potential is -0.32V this negative cell potential a value confirms thus, option (A) is incorrect.

The overall potential is zero in case of option (C) thus it is not a correct choice.

The overall potential is also negative in the case of option (B).  Thus it is also not a correct choice.

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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
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