EBK ESSENTIAL ORGANIC CHEMISTRY
EBK ESSENTIAL ORGANIC CHEMISTRY
3rd Edition
ISBN: 8220100659461
Author: Bruice
Publisher: PEARSON
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Chapter 13.1, Problem 2P

(a)

Interpretation Introduction

Interpretation: The stronger acid of the given compounds has to be found.

Concept introduction:

Electronegativity is a measure of the tendency of an atom to attract a bonding pair of electrons.  Electronegative of hybrid orbitals depends upon the % s character. Hence more the s character more the electronegativity.

The acidity depends upon the electronegativity of an atom. More the electronegativity more the acidity.

s character decreases from sp>sp2>sp3. Therefore, acidity decreases from sp>sp2>sp3.

The oxygen is more electronegative. Therefore, it attracts a shared pair of electron pair of OH bond towards itself. As a result, OH bond is more easily broken.

(b)

Interpretation Introduction

Interpretation:

The greater pKa value of the given compounds has to be found.

Concept introduction:

The ionization constant Ka of acids increases with increasing the strength of acid. The stronger the acid, higher the value of ionization constant Ka.

The relation between Ka and pKa is expressed as,

pKa= -log(Ka)

The stronger the acid, lower the value of pKa.

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Done 11:14 ⚫ worksheets.beyondlabz.com 5 (a). Using the peak information you listed in the tables for both structures, assign each peak to that portion of the structure that produces the peak in the NMR spectrum. Draw this diagram on your own sheet of paper and attach the sketch of your drawing to this question. Question 6 5 (b). Using the peak information you listed in the tables for both structures, assign each peak to that portion of the structure that produces the peak in the NMR spectrum. Draw this diagram on your own sheet of paper and attach the sketch of your drawing to this question. Question 7 6. Are there any differences between the spectra you obtained in Beyond Labz and the predicted spectra? If so, what were the differences? <
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
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