EBK EXPERIMENTAL ORGANIC CHEMISTRY: A M
EBK EXPERIMENTAL ORGANIC CHEMISTRY: A M
6th Edition
ISBN: 9781305687875
Author: Gilbert
Publisher: CENGAGE LEARNING - CONSIGNMENT
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Chapter 8.2, Problem 17E
Interpretation Introduction

Interpretation:The spectrum of acetanilide contained in a Nujol mull needs to be prepared and should be compared with the ATR spectrum. The sources of differences need to be explained.

Concept introduction:

In IR spectroscopy, the vibration of atoms is depicted as frequency in IR spectrum which is useful in predicting the functional groups and other compounds. The frequencies of different compounds falls in various ranges that is depicted in IR spectrum.

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Part 3B Set 2. Can 1H NMR spectroscopy be used to differentiate between the two compounds? Briefly explain why or why not. Predict the 1H NMR spectrum for each compound (include integration, multiplicity, and approximate chemical shift). Either draw the actual spectrum or put in a data table format.
[Review Topics] [References] Splitting of a signal in a proton NMR spectrum tells us the number of chemically non-equivalent hydrogens in the immediate vicinity of the hydrogen giving the signal. Predict the number of lines exhibited by hydrogens at the labeled positions in a first-order NMR spectrum. (Make the approximation that all coupling constants are equal.) 1) The number of lines exhibited by hydrogen(s) a is The number of lines exhibited by hydrogen(s) b is The number of lines exhibited by hydrogen(s) c is 2) The number of lines exhibited by hydrogen(s) a is The number of lines exhibited by hydrogen(s) b is The number of lines exhibited by hydrogen(s) c is Submit Answer Retry Entire Group No more group attempts remain W
Part 3B Set 1. Can 1H NMR spectroscopy be used to differentiate between the two compounds? Briefly explain why or why not. Predict the 1H NMR spectrum for each compound (include integration, multiplicity, and approximate chemical shift). Put it in data table format.
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